Synthesis and structural characterization of metal complexes with macrocyclic tetracarbene ligands

被引：17

作者：

Fei, Fan ^{[1
]}

Lu, Taotao ^{[1
]}

Chen, Xue-Tai ^{[1
]}

Xue, Zi-Ling ^{[2
]}

机构：

[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210023, Jiangsu, Peoples R China

[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA

来源：

NEW JOURNAL OF CHEMISTRY | 2017年 / 41卷 / 22期

基金：

美国国家科学基金会;

关键词：

N-HETEROCYCLIC-CARBENE; DICARBENE BUILDING-BLOCKS; TETRAIMIDAZOLIUM SALTS; COORDINATION CHEMISTRY; CATALYTIC APPLICATIONS; MOLECULAR SQUARE; NHC LIGANDS; HEME ANALOG; PI-PI; AU-I;

D O I：

10.1039/c7nj02485a

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Fourteen Ag(I), Au(I), Ni(II), Pd(II), and Pt(II) complexes with macrocyclic tetradentate N-heterocyclic carbene (NHC) ligands were prepared via reactions between three macrocyclic tetrabenzimidazolium salts and metal precursors. All except two Au complexes were characterized using single-crystal X-ray diffraction. Three different structures, including a trinuclear one containing a NHC-Ag-(H2O) moiety and a hexanuclear propeller-like supramolecular assembly, are found for Ag-NHC complexes. Nine complexes of group 10 metal ions adopt square-planar geometry, in which the different ring-sizes of the macrocyclic tetracarbene ligands lead to a variation of metal-carbene bond lengths. pi-pi stackings are observed between the rigid aromatic benzimidazole rings in the nickel group complexes.

引用

页码：13442 / 13453

页数：12

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