Electronic communication in heterobinuclear organometallic complexes through unsaturated hydrocarbon bridges

被引:308
作者
Ceccon, A [1 ]
Santi, S [1 ]
Orian, L [1 ]
Bisello, A [1 ]
机构
[1] Univ Padua, Dipartimento Chim Fis Arturo Miolati, I-35131 Padua, Italy
关键词
heterobimetallic complexes; electron transfer; molecular wires; mixed-valence chemistry; cooperative effects;
D O I
10.1016/j.ccr.2004.02.007
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Much of the interest about the construction of model compounds suitable for investigating the phenomena associated with the interaction of two or more metal centers, the so-called cooperative effect, has been concentrated on homobimetallic complexes and less attention has been paid to the class of heterobimetallic derivatives. This review will feature experimental detection and the effects of the electronic communication in heterobinuclear organometallic complexes through unsaturated hydrocarbon bridges. The described systems are classified according to the nature of the bridging ligand, in three main groups: (i) carbon sigma-bonded molecular wires; (ii) fulvalene and fulvalene-like bridges; (iii) fused delocalized polycyclic bridges. In this contribution, we discuss the flexibility of heterobimetallic complexes, and more in general of asymmetric bimetallic species, in terms of tailoring the cooperative effects, i.e. of controlling and tuning the reactivity of one metal center by acting on the adjacent one. Satisfactory quantitative estimate of the degree of metal to metal communication through the bridging ligand is obtained in illustrative examples combining efficient electrochemical and spectroscopic techniques with consolidated theories. A review with almost 350 references. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:683 / 724
页数:42
相关论文
共 336 条
[1]   HEXACARBONYL(FULVALENE)DITUNGSTEN(W-W) - A STRETCHED TUNGSTEN TUNGSTEN SINGLE BOND [J].
ABRAHAMSON, HB ;
HEEG, MJ .
INORGANIC CHEMISTRY, 1984, 23 (15) :2281-2286
[2]   SYNTHESIS AND PREPARATIVE HPLC-SEPARATION OF HETERONUCLEAR OLIGOMETALLOCENES - ISOLATION OF CATIONS OF RHODOCENYLFERROCENE, 1,1'-DIRHODOCENYLFERROCENE, AND 1-COBALTOCENYLFERROCENE,1'-RHODOCENYLFERROCENE [J].
ANDRE, M ;
SCHOTTENBERGER, H ;
TESSADRI, R ;
INGRAM, G ;
JAITNER, P ;
SCHWARZHANS, KE .
CHROMATOGRAPHIA, 1990, 30 (9-10) :543-545
[3]   From organotransition-metal chemistry toward molecular electronics: Electronic communication between ligand-bridged metals [J].
Astruc, D .
ACCOUNTS OF CHEMICAL RESEARCH, 1997, 30 (09) :383-391
[4]   19-ELECTRON COMPLEXES AND THEIR ROLE IN ORGANOMETALLIC MECHANISMS [J].
ASTRUC, D .
CHEMICAL REVIEWS, 1988, 88 (07) :1189-1216
[5]  
Astruc D., 1995, ELECT TRANSFER RAD 1
[6]  
ASTRUC D, 1995, ELECT TRANSFER RADIC, pCH4
[7]  
ASTRUC D, 1995, ELECTRON TRANSFER RA, pCH6
[8]   EVIDENCE FOR TIME-DEPENDENT VALENCE DETRAPPING IN A MIXED-VALENT DIMANGANESE FULVALENYL CATION [J].
ATWOOD, CG ;
GEIGER, WE ;
RHEINGOLD, AL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (12) :5310-5311
[9]   Investigations of time-dependent delocalization and the correlation of carbonyl IR shifts with ΔE1/2 values for hydrocarbon-linked class II and class III mixed-valent complexes [J].
Atwood, CG ;
Geiger, WE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (23) :5477-5485
[10]   Luminescent and redox-active polynuclear transition metal complexes [J].
Balzani, V ;
Juris, A ;
Venturi, M ;
Campagna, S ;
Serroni, S .
CHEMICAL REVIEWS, 1996, 96 (02) :759-833