Chemistry of coordinatively unsaturated organoruthenium amidinates as entry to homogeneous catalysis

Hideo Nagashima, Hideo Kondo, Taizo Hayashida, Yoshitaka Yamaguchi, Mitsuru Gondo, Satoshi Masuda, Kazuma Miyazaki, Kouki Matsubara, Karl Kirchner

研究成果: ジャーナルへの寄稿学術誌査読

109 被引用数 (Scopus)

抄録

The chemistry of coordinatively unsaturated organoruthenium complexes is reviewed in this article. In particular, the subject is focused on neutral and cationic organoruthenium amidinates, which formally have 16 valence electrons and show signs of coordinative unsaturation. The ruthenium amidinates, (η5-C5Me5)Ru(η-amidinate) (1), and their isoelectronic analogues, [η6-arene)Ru(η -amidinate)]+ (2), are synthesized and characterized; a possible stabilizing factor of the unsaturated metal center is weak coordination of π-electrons in the amidinates ligands. Reactions of various two-electron donor ligands with 1 or 2 reveal the strong w-donor property of 1 and Lewis acid nature of 2. One or two-electron redox processes of 1 in the reactions with organic halides are studied by isolation of the corresponding Ru(III) and Ru(IV) products; the results lead to their catalysis for the Tsuji-Trost reaction and the intramolecular Kharasch reaction. The treatment of 2 with trimethylsilyldiazomethane results in the formation of cationic amidinato-carbene complexes, which involve unusual reversible metal-to-carbon silyl group migration.

本文言語英語
ページ(範囲)177-190
ページ数14
ジャーナルCoordination Chemistry Reviews
245
1-2
DOI
出版ステータス出版済み - 10月 2003

!!!All Science Journal Classification (ASJC) codes

  • 物理化学および理論化学
  • 無機化学
  • 材料化学

フィンガープリント

「Chemistry of coordinatively unsaturated organoruthenium amidinates as entry to homogeneous catalysis」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル