Deoxydehydration of vicinal diols and polyols catalyzed by pyridinium perrhenate salts
Autor: | Mirza Cokoja, Jason B. Love, Karlotta van Rees, Fritz E. Kühn, Fernanda Duarte, Danny S. Morris, Massimiliano Curcio |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
inorganic chemicals
Perrhenate 010405 organic chemistry organic chemicals Diol chemistry.chemical_element Rhenium 010402 general chemistry 01 natural sciences Catalysis 0104 chemical sciences chemistry.chemical_compound chemistry Polymer chemistry Organic chemistry Ammonium heterocyclic compounds Pyridinium Vicinal Phosphine |
Zdroj: | 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 |
ISSN: | 2044-4761 2044-4753 |
DOI: | 10.1039/C7CY01728F |
Popis: | 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, outperforming primary, secondary, and tertiary ammonium salts, while quaternary ammonium salts are effectively inactive. The mechanism of reaction was studied computationally using DFT calculations which indicate that proton shuttling between the ion pair is intrinsic to the mechanism and that the reduction of rhenium by the phosphine occurs before the diol condensation. |
Databáze: | OpenAIRE |
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