Synthesis of d10 N-Heterocyclic Carbene Complexes with a Perimidine Scaffold

被引:8
作者
Strausser, Shelby L. [1 ]
Jenkins, David M. [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
基金
美国国家科学基金会;
关键词
TRANSITION-METAL-COMPLEXES; H BOND ACTIVATION; IRIDIUM COMPLEXES; NHC COMPLEXES; CATALYSTS; LIGANDS; RUTHENIUM; PALLADIUM; REACTIVITY; NICKEL(0);
D O I
10.1021/acs.organomet.1c00189
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
N-Heterocyclic carbenes (NHCs) are vital auxiliary ligands for organometallic chemistry, and although many variants have been synthesized, by far the most common are based on fivemembered rings, such as imidazole or benzimidazole. Unlike NHC complexes built on five-membered rings, which are typically conjugated, exploration of six-membered-ring NHC variants has focused on nonconjugated versions, such as N,N'-diamidocarbenes. Reports of conjugated six-membered ring NHCs are limited to metal complexes with a perimidine scaffold that are in a narrow range of between six and eight d electrons (on metals from groups 8-10). This manuscript showcases the synthesis of four d(10) metal complexes with a perimidine scaffold. The gold and silver complexes have a linear geometry, while the copper and platinum complexes are three-coordinated. All complexes were characterized by single-crystal X-ray crystallography, multinuclear NMR, and additional spectroscopic methods.
引用
收藏
页码:1706 / 1712
页数:7
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