Synthesis of asymmetric supramolecular compounds using a Ni(0) catalysed homo-coupling approach

被引:10
作者
Cassidy, Lynda [1 ]
Horn, Sabine [1 ]
Cleary, Laura [1 ]
Halpin, Yvonne [1 ]
Browne, Wesley R. [2 ]
Vos, Johannes G. [1 ]
机构
[1] Dublin City Univ, Sch Chem Sci, Solar Energy Convers SRC, Dublin 9, Ireland
[2] Univ Groningen, Stratingh Inst Chem, Ctr Syst Chem, NL-9747 AG Groningen, Netherlands
基金
爱尔兰科学基金会;
关键词
ELECTROCHEMICAL PROPERTIES; POLYPYRIDINE COMPLEXES; RUTHENIUM; CHEMISTRY; LIGAND; DEUTERIATION; STATE;
D O I
10.1039/b817896h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and characterisation of a series of dinuclear ruthenium and osmium polypyridyl metal complexes based on the bridging ligands [5-(5'-bipyridin-2',2 ''-yl)-3-(pyridin-2-yl)]-1,2,4-triazole (Hpytr-bipy), 2,2 ''-bis(pyridin-2 '' yl)-5,5 ''-bis(pyridin-3 ''-yl) (bipy-bipy) and 5,5'-bis(pyridin-2 ''-yl)-3,3'-bis(1,2,4-triazole) (Hpytr-Hpytr) are reported. The dinuclear complexes have been synthesised via a Ni(0) catalysed cross-coupling reaction from brominated precursors. With this approach a mixture of three products is obtained, which are separated by chromatographic methods. The compounds obtained are characterised by elemental analysis, H-1 NMR, absorption and emission spectroscopy. The synthetic approach developed offers a new route to asymmetric multinuclear supramolecular structures that is complimentary to the complexes as ligands/complexes as metal approaches.
引用
收藏
页码:3923 / 3928
页数:6
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