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Synthesis and Systematic Structural Analysis of Cationic Half-Sandwich Ruthenium Chalcogenocarbonyl Complexes
Authors:Ayumi Suzuki  Dr. Yuichiro Mutoh  Dr. Noriko Tsuchida  Chi-Wai Fung  Dr. Shoko Kikkawa  Prof. Isao Azumaya  Prof. Shinichi Saito
Affiliation:1. Department of Chemistry, Faculty of Science, Tokyo University of Science, 1–3, Kagurazaka, Shinjuku-ku, Tokyo, 162-8601 Japan;2. Department of Liberal Arts, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-machi, Iruma-gun, Saitama, 350-0495 Japan;3. Faculty of Pharmaceutical Sciences, Toho University, 2-2-3 Miyama, Funabashi-shi, Chiba, 274-8510 Japan
Abstract:Although the chemistry of transition-metal complexes with carbonyl (CO) and thiocarbonyl (CS) ligands has been well developed, their heavier analogues, namely selenocarbonyl (CSe) and tellurocarbonyl (CTe) complexes remain scarce. The limited availability of such CSe and CTe complexes has so far hampered our understanding of the differences between such chalcogenocarbonyl (CE: E=O, S, Se, Te) ligands. Herein, we report the synthesis and properties of a series of cationic half-sandwich ruthenium CE complexes of the type [CpRu(CE)(H2IMes)(CNCH2Ts)][BArF4] (Cp=η5-C5H5; H2IMes=1,3-dimesitylimidazolin-2-ylidene; ArF=3,5-(CF3)2C6H3). A combination of X-ray diffraction analyses, NMR spectroscopic analyses, and DFT calculations revealed an increasing π-accepting ability of the CE ligands in the order O
Keywords:carbene ligands  carbon chalcogenide  chalcogens  chiral-at-metal  tellurocarbonyl
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