New 2,2′:4,4":4′,4′"-quaterpyridyl transition metal complexes

被引:12
|
作者
de Wolf, P
Heath, SL [1 ]
Thomas, JA
机构
[1] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
[2] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
关键词
complexes-as-ligands; electrochemistry; luminescence;
D O I
10.1016/S0020-1693(03)00370-0
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of the previously reported 2,2':4,4":4',4"'-quaterpyridyl ligand, with d(6) Re-1 and d(8) Pd-11 and Pt-11 metal centres has been investigated. This has lead to the synthesis, isolation and characterisation of seven new complexes. The UV-Vis absorption spectra of the new complexes are dominated by intraligand and charge transfer bands. While the d(8) metal complexes are not emissive, the Re-1 complexes display broad unstructured luminescence that is consistent with emission from a Re(d) --> diimine(pi*) manifold. Electrochemical studies reveal that the d(8) metal complexes and one of the Re-1 complexes only display irreversible ligand based reductions. However the remaining two other Re-1 complexes display chemically irreversible metal based oxidations. The photophysical and electrochemical properties of the complexes have been rationalised by a consideration of the sigma- and pi-donor/acceptor characteristics of the ligands. (C) 2003 Elsevier B.V. All rights reserved.
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页码:280 / 285
页数:6
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