Early-Late Heterobimetallic Complexes with a Ta-Ir Multiple Bond: Bimetallic Oxidative Additions of C-H, N-H, and O-H Bonds

被引：22

作者：

Oishi, Masataka ^{[1
]}

Kino, Masashi ^{[1
]}

Saso, Masayuki ^{[1
]}

Oshima, Masato ^{[2
]}

Suzuki, Hiroharu ^{[1
]}

机构：

[1] Tokyo Inst Technol, Grad Sch Sci & Engn, Meguro Ku, Tokyo 1528552, Japan

[2] Tokyo Polytech Univ, Sch Engn, Atsugi, Kanagawa 2430297, Japan

来源：

ORGANOMETALLICS | 2012年 / 31卷 / 13期

基金：

日本学术振兴会;

关键词：

METAL BOND; REACTIVITY; TANTALUM; ACTIVATION; LIGAND; ALCOHOLS; HYDRIDO; WATER; ZR;

D O I：

10.1021/om300429u

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A heterobinuclear transition metal complex with a Ta-Ir multiple bond, Cp*(Me3SiCH2)(2)Ta-IrCp*(H)(2) (1), was synthesized using a salt elimination reaction. The isolable complex was characterized by NMR, IR, UV-vis spectroscopy, and X-ray crystallography. Compound I features an exceptionally short intermetallic distance (Ta-Ir 2.4457(3) angstrom). DFT calculation for 1 revealed the presence of a highly covalent bonding nature in spite of the involvement of such disparate d elements. Oxidative additions of C-H, N-H, and O-H bonds to 1 were also investigated.

引用

页码：4658 / 4661

页数：4

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