Affiliation:
1. Department of Chemistry Graduate School of Science Tohoku University 6-3 Aoba Sendai Miyagi 980–8578 Japan
2. Department of Applied Chemistry Faculty of Science and Engineering Kindai University 3-4-1 Kowakae Higashi Osaka, Osaka 577-8502 Japan
Abstract
AbstractA neutral silylyne complex with a Cr≡Si triple bond was prepared by dehydrogenation of a chromium silylene complex with Cr−H and Si−H bonds, and was isolated as monomeric crystals, unlike dimeric forms of its tungsten and molybdenum congeners. The strong Cr(δ−)−Si(δ+) bond polarity was revealed by the reaction with MeOH and DFT calculations. The chromium silylyne complex reacted with H2 under LED (365 nm) irradiation to reproduce the precursor silylene complex with a (H)Cr=Si(H) moiety, as a result of 1,2‐H−H addition across the Cr≡Si triple bond. Similarly, the chromium silylyne complex reacted with benzene under irradiation to afford an 1,2‐addition product with a (H)Cr=Si(Ph) moiety, via benzene C−H bond activation accompanied by Si−C bond forming.
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
1 articles.
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