Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Danny S. Morris"'
Autor:
Peter A. Tasker, Mirza Cokoja, Fritz E. Kühn, Michael H. Anthofer, Saner Poplata, Jason B. Love, Wolfgang A. Herrmann, Alexander Pöthig, Iulius I. E. Markovits, Danny S. Morris
Publikováno v:
Cokoja, M, Markovits, I I E, Anthofer, M H, Poplata, S, Pöthig, A, Morris, D S, Tasker, P A, Herrmann, W A, Kühn, F E & Love, J B 2015, ' Catalytic epoxidation by perrhenate through the formation of organic-phase supramolecular ion pairs ', Chemical Communications, vol. 51, pp. 3399-3402 . https://doi.org/10.1039/c4cc10235e
Organic-phase supramolecular ion pair (SIP) host-guest assemblies of perrhenate anions (ReO4(-)) with ammonium amide receptor cations are reported. These compounds act as catalysts for the epoxidation of alkenes by aqueous hydrogen peroxide under bip
Autor:
Mirza Cokoja, Jason B. Love, Karlotta van Rees, Fritz E. Kühn, Fernanda Duarte, Danny S. Morris, Massimiliano Curcio
Publikováno v:
Morris, D S, Van Rees, K, Curcio, M, Cokoja, M, Kühn, F E, Love, J B & Duarte Gonzalez, F 2017, ' Deoxydehydration of vicinal diols and polyols catalyzed by pyridinium perrhenate salts ', Catalysis Science & Technology . https://doi.org/10.1039/C7CY01728F
Simple ammonium and pyridinium perrhenate salts were evaluated as catalysts for the deoxydehydration (DODH) of diols into alkenes. Pyridinium perrhenates were found to be effective catalysts at much lower temperatures than those in previous reports,
Autor:
Julian T. C. Wennmacher, Jason B. Love, Markus Drees, Mirza Cokoja, Catherine Weetman, Fritz E. Kühn, Danny S. Morris
Publikováno v:
Morris, D S, Weetman, C, Wennmacher, J T C, Cokoja, M, Drees, M, Kühn, F E & Love, J B 2017, ' Reduction of carbon dioxide and organic carbonyls by hydrosilanes catalysed by the perrhenate anion ', Catalysis Science & Technology . https://doi.org/10.1039/C7CY00772H
The simple perrhenate salt [N(hexyl)4][(ReO4)] acts as a catalyst for the reduction of organic carbonyls and carbon dioxide by primary and secondary hydrosilanes. In the case of CO2, this results in the formation of methanol equivalents via silylform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cf787d2c595fabc8583742790cd40b7
https://strathprints.strath.ac.uk/73738/1/Morris_etal_CST_2017_Reduction_of_carbon_dioxide_and_organic_carbonyls_by_hydrosilanes.pdf
https://strathprints.strath.ac.uk/73738/1/Morris_etal_CST_2017_Reduction_of_carbon_dioxide_and_organic_carbonyls_by_hydrosilanes.pdf
Autor:
Iulius I. E. Markovits, Fritz E. Kühn, Jason B. Love, Johannes Schäffer, Michael H. Anthofer, Marlene Kaposi, Christian J. Münchmeyer, Mirza Cokoja, Michael E. Wilhelm, Wolfgang A. Herrmann, Andreas Jess, Danny S. Morris, Robert M. Reich
Publikováno v:
Cokoja, M, Reich, R M, Wilhelm, M E, Kaposi, M, Schaeffer, J, Morris, D S, Muenchmeyer, C J, Anthofer, M H, Markovits, I I E, Kuehn, F E, Herrmann, W A, Jess, A & Love, J B 2016, ' Olefin Epoxidation in Aqueous Phase Using Ionic-Liquid Catalysts ', Chemsuschem, vol. 9, no. 14, pp. 1773-1776 . https://doi.org/10.1002/cssc.201600373
Hydrophobic imidazolium-based ionic liquids (IL) act as catalysts for the epoxidation of unfunctionalized olefins in water using hydrogen peroxide as oxidant. Although the catalysts are insoluble in both the substrate and in water, surprisingly, they