\n\t\t\t\t\t\t\t\t\n\t\t\t\tERC Carboflow \n\t\t\t<\/h2 > \n\t\t\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLatest Publications<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/schroeder-lab-research-left-img.png\")
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/schroeder-lab-about-katharina-schroder-left.png\")
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tERC Consolidator Grant 2019: CARBOFLOW<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tCARBOFLOW: Streamlined CO2<\/sub> conversion - a platform strategy for modern carbonylation chemistry<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tHardly any industrial process can utilize CO2<\/sub> directly as a raw material, but why is it so difficult to turn CO2<\/sub> into something useful? Due to the highest oxidized state of carbon, CO2<\/sub> is so stable that it can be even used as fire extinguisher, and potent catalysts are required to overcome its thermodynamic and kinetic barrier.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t![\"ERC](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2024\/01\/ERC-carboflow-Picture-1.png\")
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tThe ERC-funded project CARBOFLOW focuses on the photocatalytic reduction of CO2<\/sub> to CO and its valorization into high-value bulk and fine chemicals.\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t![\"Carboflow](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/03\/Carboflow-illustration-1024x404.png\")
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tSeveral goals need to be realised, including fundamental studies and optimisation of the co-catalysed photocatalytic reduction of carbon dioxide to produce CO under mild conditions (Goal 1). The reactivity of formed CO in supercritical carbon dioxide with various organic substrates needs to be explored (Goal 2) before finally developing a streamlined and continuous process for the direct formation of carbonyl compounds from carbon dioxide (Goal 3).\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2024\/01\/photocatalytic-reduction-of-carbon-dioxide.png\")
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tWe envision that the photocatalytic activation of carbon dioxide in combination with the positive features of tailored ionic liquids as co-catalysts may overcome problems currently associated with CO2<\/sub> utilization, eventually replacing the long-standing bastion of CO-based carbonylation chemistry with novel solutions.\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Florian Ehrschwendtner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOrg. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/Org_Biomol_Chem_2022_20_7245.png\")
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSurface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/J_Mol_Liq_2022_347_118160.png\")
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/ChemSusChem_202215_e202102262.png\")
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/Green_Chem_Lett_Rev_2022_15_405.png\")
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/Angew_Chem_Int_Ed_2022_61_e202202189.png\")
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
![\"\"](\"https:\/\/info.ias.tuwien.ac.at\/schroederlab\/wp-content\/uploads\/2023\/02\/J_Org_Chem_2022_87_11042.png\")
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
Latest Publications<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tERC Consolidator Grant 2019: CARBOFLOW<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tCARBOFLOW: Streamlined CO2<\/sub> conversion - a platform strategy for modern carbonylation chemistry<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tHardly any industrial process can utilize CO2<\/sub> directly as a raw material, but why is it so difficult to turn CO2<\/sub> into something useful? Due to the highest oxidized state of carbon, CO2<\/sub> is so stable that it can be even used as fire extinguisher, and potent catalysts are required to overcome its thermodynamic and kinetic barrier.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tThe ERC-funded project CARBOFLOW focuses on the photocatalytic reduction of CO2<\/sub> to CO and its valorization into high-value bulk and fine chemicals.\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tSeveral goals need to be realised, including fundamental studies and optimisation of the co-catalysed photocatalytic reduction of carbon dioxide to produce CO under mild conditions (Goal 1). The reactivity of formed CO in supercritical carbon dioxide with various organic substrates needs to be explored (Goal 2) before finally developing a streamlined and continuous process for the direct formation of carbonyl compounds from carbon dioxide (Goal 3).\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tWe envision that the photocatalytic activation of carbon dioxide in combination with the positive features of tailored ionic liquids as co-catalysts may overcome problems currently associated with CO2<\/sub> utilization, eventually replacing the long-standing bastion of CO-based carbonylation chemistry with novel solutions.\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Florian Ehrschwendtner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOrg. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSurface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\tERC Consolidator Grant 2019: CARBOFLOW<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tCARBOFLOW: Streamlined CO2<\/sub> conversion - a platform strategy for modern carbonylation chemistry<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tHardly any industrial process can utilize CO2<\/sub> directly as a raw material, but why is it so difficult to turn CO2<\/sub> into something useful? Due to the highest oxidized state of carbon, CO2<\/sub> is so stable that it can be even used as fire extinguisher, and potent catalysts are required to overcome its thermodynamic and kinetic barrier.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tThe ERC-funded project CARBOFLOW focuses on the photocatalytic reduction of CO2<\/sub> to CO and its valorization into high-value bulk and fine chemicals.\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tSeveral goals need to be realised, including fundamental studies and optimisation of the co-catalysed photocatalytic reduction of carbon dioxide to produce CO under mild conditions (Goal 1). The reactivity of formed CO in supercritical carbon dioxide with various organic substrates needs to be explored (Goal 2) before finally developing a streamlined and continuous process for the direct formation of carbonyl compounds from carbon dioxide (Goal 3).\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tWe envision that the photocatalytic activation of carbon dioxide in combination with the positive features of tailored ionic liquids as co-catalysts may overcome problems currently associated with CO2<\/sub> utilization, eventually replacing the long-standing bastion of CO-based carbonylation chemistry with novel solutions.\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Florian Ehrschwendtner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOrg. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSurface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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CARBOFLOW: Streamlined CO2<\/sub> conversion - a platform strategy for modern carbonylation chemistry<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tHardly any industrial process can utilize CO2<\/sub> directly as a raw material, but why is it so difficult to turn CO2<\/sub> into something useful? Due to the highest oxidized state of carbon, CO2<\/sub> is so stable that it can be even used as fire extinguisher, and potent catalysts are required to overcome its thermodynamic and kinetic barrier.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tThe ERC-funded project CARBOFLOW focuses on the photocatalytic reduction of CO2<\/sub> to CO and its valorization into high-value bulk and fine chemicals.\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tSeveral goals need to be realised, including fundamental studies and optimisation of the co-catalysed photocatalytic reduction of carbon dioxide to produce CO under mild conditions (Goal 1). The reactivity of formed CO in supercritical carbon dioxide with various organic substrates needs to be explored (Goal 2) before finally developing a streamlined and continuous process for the direct formation of carbonyl compounds from carbon dioxide (Goal 3).\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tWe envision that the photocatalytic activation of carbon dioxide in combination with the positive features of tailored ionic liquids as co-catalysts may overcome problems currently associated with CO2<\/sub> utilization, eventually replacing the long-standing bastion of CO-based carbonylation chemistry with novel solutions.\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Florian Ehrschwendtner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOrg. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSurface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
Hardly any industrial process can utilize CO2<\/sub> directly as a raw material, but why is it so difficult to turn CO2<\/sub> into something useful? Due to the highest oxidized state of carbon, CO2<\/sub> is so stable that it can be even used as fire extinguisher, and potent catalysts are required to overcome its thermodynamic and kinetic barrier.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\tPhotocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Florian Ehrschwendtner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOrg. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSurface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
Org. Biomol. Chem. (2022<\/strong>) 20, 7245<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
Herein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and para-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
Surface-active ionic liquids: A review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Alice Cognigni, Christian Schr\u00f6der, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tLiquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
J. Mol. Liq. (2022<\/strong>) 347, 118160<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
The combination of water and surface-active ionic liquids provides a unique reaction medium, facilitating aggregation and micellization of the ionic liquid to allow for chemical reactions in bulk water. With a growing focus on sustainable technologies, ionic liquids have emerged as tunable solvents for multiple applications but are often too viscous or expensive for use as bulk solvent. As a result, there has been a tremendous increase in interest in the behavior of ionic liquids in the presence of water. It has already been shown that certain ionic liquids act as surfactants in aqueous solutions, enabling the combination of both solvents to afford solvent systems with unique properties. Ultimately, surface-active ionic liquids in water give rise to distinct chemistry of their own compared to traditional molecular solvents, and thus their use is rapidly growing. In this review, the general structure of surface-active ionic liquids and the key features that allow aggregation in water to give micellar structures is discussed. Furthermore, characterization techniques of the formed micelles are presented, discussing aggregation and possible methods of studying micellization behavior. Finally, current applications of surface-active ionic liquids across all fields of chemistry, from traditional organic chemistry to nanoparticle synthesis are presented.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
Liquid- and Solid-based Separations Employing Ionic Liquids for the Recovery of Platinum Group Metals Typically Encountered in Catalytic Converters: A Review<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Michael Schn\u00fcrch, Andreas Limbeck, Katharina Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tBenign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
ChemSusChem (2022<\/strong>) 15, e202102262<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
The wide application range and ascending demand for platinum group metals combined with the progressive depletion of their natural resources renders their efficient recycling a very important and pressing matter. Primarily environmental considerations associated with state-of-the-art recovery processes have shifted the focus of the scientific community toward the investigation of alternative recycling approaches. Within this context, ionic liquids have gained considerable attention in the last two decades chiefly sparked by properties such as tunabilty, low-volatility, and relatively easy recyclability. In this review an understanding of the state-of-the-art processes, including their drawbacks and limitations, is provided. The core of the discussion is focused on platinum group metal recovery with ionic liquid-based systems. A brief insight in some environmental considerations related to ionic liquids is also provided while some discussion on research gaps, common misconceptions related to ionic liquids and outlook on unresolved issues could not be absent from this review.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
Benign recovery of platinum group metals from spent automotive catalysts using choline-based deep eutectic solvents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tOlga Lanaridi, Sonja Platzer, Winfried Nischkauer, Jokin Hidalgo Betanzos, Ainhoa Unzurrunzaga Iturbe, Carmen Del Rio Gaztelurrutia, Laura Sanchez-Cupido, Amal Siriwardana, Michael Schn\u00fcrch, Andreas Limbeck, Thomas Konegger, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tGreen Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tThe recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tSterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
Green Chem. Lett. Rev. (2022<\/strong>) 15, 405<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
The recovery of platinum group metals (PGMs) from secondary raw materials has become a topic ofcritical importance mainly due to the gradual depletion of their natural resources and theircontinuously increasing demand. However, the insufficient recovery of PGMs coupled with thenegative environmental impact of the state-of-the-art recycling procedures mandate theinvestigation and development of alternative recovery processes that will assist in minimizing oreven eliminating these drawbacks. Herein, we present a process for the extraction of platinumgroup metals from spent car catalysts relying on benign deep eutectic solvents (DESs). It isdemonstrated that with addition of small amounts of an oxidizing agent, deep eutectic solventscan act as excellent leaching media for the quantitative extraction of platinum group metals.Despite its inertness towards acidic and oxidizing agents, Rh can be leached in a considerableamount which can be further increased by physical pre-treatment of the spent car catalystmaterial.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
Sterically Demanding Flexible Phosphoric Acids for Constructing Efficient and Multi-Purpose Asymmetric Organocatalysts<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tFabian Scharinger, \u00c1d\u00e1m M\u00e1rk P\u00e1lv\u00f6lgyi, Melanie Weisz, Matthias Weil, Christian Stanetty, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tAngew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHerein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\tPhotocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
<\/p>
\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
\n\t\t\t\t\t\t
Angew. Chem. Int. Ed. (2022<\/strong>) 61, e202202189<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
Herein, we present a novel approach for various asymmetric transformations of cyclic enones. The combination of readily accessible chiral diamines and sterically demanding flexible phosphoric acids resulted in a simple and highly tunable catalyst framework. The careful optimization of the catalyst components led to the identification of a particularly powerful and multi-purpose organocatalyst, which was successfully applied for asymmetric epoxidations, aziridinations, aza-Michael-initiated cyclizations, as well as for a novel Robinson-like Michael-initiated ring closure\/aldol cyclization. High catalytic activities and excellent stereocontrol was observed for all four reaction types, indicating the excellent versatility of our catalytic system. Furthermore, a simple change in the diamine\u2019s configuration provided easy access to both product antipodes in all cases.<\/p>
<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
Photocatalytic Hydroalkylation of Aryl-Alkenes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tCornelia S. Buettner, Michael Schn\u00fcrch, Katharina Bica-Schr\u00f6der*\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\t\tJ. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\t\t\t\t\t\t\t\tAbstract<\/a>\n\t\t\t\t\t<\/div>\n\n\t\t\t\t\tHere, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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J. Org. Chem. (2022<\/strong>) 87, 11042<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
Here, we present a visible light-catalyzed hydroalkylation of aryl-alkenes affording C\u2013C bonds using aryl-alkenes and alkyl iodides. We demonstrate the formation of various hydroalkylation products in excellent yields, with primary, secondary, and tertiary alkyl iodides being tolerated in the reaction. Mechanistic experiments reveal a pathway consisting of halogen atom transfer followed by a radical-polar crossover mechanism delivering the desired hydroalkylation products.<\/p>
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\u00a0<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t