Bimetallic Cu(I) complex with a pyridine-bridged bis(1,2,3-triazole-5-ylidene) ligand

被引：24

作者：

Iwasaki, Haruka ^{[1
]}

Teshima, Yuta ^{[1
]}

Yamada, Yuji ^{[1
]}

Ishikawa, Ryuta ^{[1
]}

Koga, Yuji ^{[1
]}

Matsubara, Kouki ^{[1
]}

机构：

[1] Fukuoka Univ, Dept Chem, Jonan Ku, 8-19-1 Nanakuma, Fukuoka 8140180, Japan

来源：

DALTON TRANSACTIONS | 2016年 / 45卷 / 13期

基金：

日本学术振兴会;

关键词：

N-HETEROCYCLIC CARBENES; CU-CATALYZED HYDROBORATION; METAL-COMPLEXES; CARBON-DIOXIDE; PINCER LIGAND; BEARING; BONDS;

D O I：

10.1039/c6dt00008h

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A dinuclear copper(I) complex bearing a mesoionic carbene ligand has been prepared from the corresponding silver analogue and its structure determined spectroscopically. The results revealed that two Cu(I) halide salt molecules were bound to the carbon atoms of the pyridine-bridged bis(triazolylidene) moieties rather than the pyridine. Cyclic voltammogram measurements revealed that the two Cu(I) centres underwent a stepwise oxidation, suggesting that both the triazolylidene rings of the ligand could be on the same expanded pi-conjugated system. The catalytic hydroboration of styrene derivatives with bis(pinacolato) diborane in the presence of this complex allowed for the beta-selective formation of the corresponding alkylboronate esters.

引用

页码：5713 / 5719

页数：7

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