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作 者:Peng-Fei Cui Yang Gao Shu-Ting Guo Guo-Xin Jin
机构地区:[1]Department of Chemistry,Fudan University,State Key Laboratory of Molecular Engineering of Polymers,Shanghai,200433 China [2]State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai,200032 China
出 处:《Chinese Journal of Chemistry》2021年第2期281-287,共7页中国化学(英文版)
基 金:This work was supported by the National Natural Science Foun-dation of China(Nos.21531002,21720102004,22031003);the Shanghai Science Technology Committee(No.13JC1400600).
摘 要:We report herein a practical approach for regio-selective B—H/C—H bond activation at azo-substituted carboranes. The reaction proceeded through Iridium(III)-induced selective B—H/C—H bond activations based on an azo directing group. Through this strategy, a series of mononuclear, trinuclear and tetranuclear cyclometalated iridium complexes containing Cp*Ir—B or Cp*Ir—C bonds were successfully isolated in a high yield. In this work, efficient routes are developed through one-pot reactions to prepare polynuclear organometallic complexes.
关 键 词:CARBORANE B-H bond activation HALF-SANDWICH IRIDIUM POLYNUCLEAR
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