Functional metal complexes based on bridging "imino"-quinonoid ligands

被引:80
|
作者
Sarkar, Biprajit [1 ]
Schweinfurth, David [1 ]
Deibel, Naina [1 ]
Weisser, Fritz [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
关键词
Bridging quinones; Redox-active ligands; NIR electrochromism; Bond activation reactions; Electrochemistry; INDUCED ELECTRON-TRANSFER; DONOR-ACCEPTOR SYSTEMS; MULTIPLE-ATOM BRIDGES; MAGNETIC-PROPERTIES; DINUCLEAR COBALT; SPIN-CROSSOVER; MIXED-VALENCY; ELECTROCHEMICAL PROPERTIES; CATALYTIC OLIGOMERIZATION; DIRUTHENIUM COMPLEXES;
D O I
10.1016/j.ccr.2015.01.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
2,5-Dihydroxy-1,4-benzoquinone (dhbq) has been extensively used as a ligand for generating mono and polynuclear complexes. In recent years, new ligand classes have been developed where one or more of the "O" groups of the dhbq unit have been replaced with isoelectronic "NR" groups. The resulting ligands have been used for synthesizing dinuclear assemblies that have been utilized for investigating metal-metal interaction, generation of electrochromic NIR dyes, studies of unusual chemical reactivity, for small molecule activation and for homogenously catalysis. Additionally, these ligand platforms have also been used for studying spin-spin coupling and for the generation of switchable molecular magnetic materials. In the following, we report on the recent developments on the generation of functional metal complexes with this ligand class, with a particular focus on the ligands with [O, N, O, NI donor sets based on a 2,5-di-[(substituted)-anilino]-1,4-benzoquinone platform. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:250 / 262
页数:13
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