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PBP钳形铱配合物的合成:一个辅助硼基配体。

Syntheses of PBP pincer iridium complexes: a supporting boryl ligand.

作者信息

Segawa Yasutomo, Yamashita Makoto, Nozaki Kyoko

机构信息

Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo 7-3-1, Hongo, Bunkyo-ku, 113-8656 Tokyo, Japan.

出版信息

J Am Chem Soc. 2009 Jul 8;131(26):9201-3. doi: 10.1021/ja9037092.

Abstract

We synthesized a PBP pincer ligand precursor 2 and demonstrated its complexation with iridium(I) to afford the coordinatively unsaturated PBPchloroiridium complex 3 via B-H oxidative addition. The reaction of 3 with carbon monoxide produced PBPchloro(carbonyl)iridium 7. The longer Ir-Cl bond length of 7 than that of 8 revealed a stronger sigma-donor ability of the PBP ligand than that of PCP. Complex 3 was also converted to PBPiridium(I) complex 9 by the reaction with LiTMP under an ethylene atmosphere.

摘要

我们合成了一种PBP钳形配体前体2,并证明了它与铱(I)的络合作用,通过B-H氧化加成得到配位不饱和的PBP氯铱络合物3。3与一氧化碳反应生成了PBP氯(羰基)铱7。7的Ir-Cl键长比8的长,这表明PBP配体的σ供体能力比PCP的更强。在乙烯气氛下,3与LiTMP反应还可转化为PBP铱(I)络合物9。

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