Cationic Silica‐Supported N‐Heterocyclic Carbene Tungsten Oxo Alkylidene Sites: Highly Active and Stable Catalysts for Olefin Metathesis |
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Authors: | Margherita Pucino Dr. Victor Mougel Roman Schowner Dr. Alexey Fedorov Prof. Dr. Michael R. Buchmeiser Prof. Dr. Christophe Copéret |
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Affiliation: | 1. Department of Chemistry and Applied Biosciences, ETH Zürich, Zurich, Switzerland;2. Institute of Polymer Chemistry, University of Stuttgart, Stuttgart, Germany |
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Abstract: | Designing supported alkene metathesis catalysts with high activity and stability is still a challenge, despite significant advances in the last years. Described herein is the combination of strong σ‐donating N‐heterocyclic carbene ligands with weak σ‐donating surface silanolates and cationic tungsten sites leading to highly active and stable alkene metathesis catalysts. These well‐defined silica‐supported catalysts, [(≡SiO)W(=O)(=CHCMe2Ph)(IMes)(OTf)] and [(≡SiO)W(=O)(=CHCMe2Ph)(IMes)+][B(ArF)4?] [IMes=1,3‐bis(2,4,6‐trimethylphenyl)‐imidazol‐2‐ylidene, B(ArF)4=B(3,5‐(CF3)2C6H3)4] catalyze alkene metathesis, and the cationic species display unprecedented activity for a broad range of substrates, especially for terminal olefins with turnover numbers above 1.2 million for propene. |
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Keywords: | metathesis N-heterocyclic carbene structure elucidation supported catalysts tungsten |
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