Synthesis, structure, redox property and ligand replacement reaction of ruthenium(II) complexes containing a terpyridyl ligand with a redox active moiety

被引:7
|
作者
Oyama, Dai [1 ]
Kido, Masato [1 ]
Orita, Ai [2 ]
Takase, Tsugiko
机构
[1] Fukushima Univ, Grad Sch Sci & Technol, Fukushima 9601296, Japan
[2] Fukushima Univ, Fac Educ, Fukushima 9601296, Japan
关键词
Ruthenium complex; Terpyridine; Crystal structure; Redox property; Ligand replacement reaction; TRANSITION-METAL-COMPLEXES; ELECTROCHEMICAL REDUCTION; PHOTOPHYSICAL PROPERTIES; SPECTROSCOPIC PROPERTIES; POLYPYRIDINE COMPLEXES; CARBONYL-COMPLEXES; ELECTRON-TRANSFER; CRYSTAL-STRUCTURE; BRIDGING LIGAND; EXCITED-STATES;
D O I
10.1016/j.poly.2009.12.024
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Ruthenium(II) complexes bearing a redox-active tridentate ligand 4'-(2,5-dimethoxyphenyl)-2,2':6',2 ''-terpyridine (tpyOMe), analogous to terpyridine, and 2,2'-bipyridine (bpy) were synthesized by the sequential replacement of Cl by CH(3)CN and CO on the complex. The new ruthenium complexes were characterized by various methods including IR and NMR. The molecular structures of [Ru(tpyOMe)(bpy)(CH(3)CN)](2+) and two kinds of [Ru(tpyOMe)(bpy)(CO)](2+) were determined by X-ray crystallography. The incorporation of monodentate ligands (Cl, CH(3)CN and CO) regulated the energy levels of the MLCT transitions and the metal-centered redox potentials of the complexes. The kinetic data observed in this study indicates that the ligand replacement reaction of [Ru(tpyOMe)(bpy)Cl](+) to [Ru(tpyOMe)(bpy)(CH(3)CN)](2+) proceeds by a solvent-assisted dissociation process. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1337 / 1343
页数:7
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