ReI(CO)3 complexes with diimine ligands synthesized in situ

被引:16
|
作者
Villafane, Fernando [1 ]
机构
[1] Univ Valladolid, Fac Ciencias, GIR MIOMeT IU Cinquima, Quim Inorgan, Campus Miguel Delibes, E-47011 Valladolid, Spain
关键词
Coupling reactions; Diimines; In situ synthesis; Rhenium; Tridentate ligands; TRANSITION-METAL-COMPLEXES; RHENIUM(I) TRICARBONYL COMPLEXES; N-HETEROCYCLIC CARBENES; LOWEST EXCITED-STATE; POLYPYRIDYL COMPLEXES; CARBONYL-COMPLEXES; CHARGE-TRANSFER; LUMINESCENCE; MOLYBDENUM; MANGANESE;
D O I
10.1016/j.ccr.2017.03.010
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This work covers the coupling reactions of monodentate ligands coordinated to the "Re-I(CO)(3)" moiety to afford in situ new bidentate diimine ligands.Similar reactions leading to tridentate ligands are also included.The reactions reviewed present evident advantages respect to the usual synthetic methods of these ligands.Besides, choosing the appropriate substituents allows an easy tuning of the properties of the final complexes.Following an approximate chronological order, the formation of bidentate ligands by C-N coupling from a coordinated carbonyl group, from diiminoisoindoline, and the formation of amidino ligands from nitriles are reviewed first.This is followed by the formation of bidentate ligands by C-C coupling, and finally by the formation of tridentate ligands, either by C-C coupling, by B-N coupling, or by using "click" reactions. (C) 2017 Elsevier B.V.All rights reserved.
引用
收藏
页码:128 / 137
页数:10
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