Synthesis, characterization and crystal structure of [Ru(tppz)(4,4'-(CH3)(2)bpy)Cl](PF6), (tppz=2,3,5,6-tetrakis(2-pyridyl)pyrazine)

被引:25
作者
Tondreau, V
Leiva, AM
Loeb, B
Stultz, LK
Meyer, TJ
机构
[1] PONTIFICIA UNIV CATOLICA CHILE, FAC QUIM, SANTIAGO, CHILE
[2] UNIV CHILE, FAC CIENCIAS FIS & MATEMAT, DEPT FIS, SANTIAGO, CHILE
[3] UNIV N CAROLINA, DEPT CHEM, CHAPEL HILL, NC 27599 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/0277-5387(95)00448-3
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis and characterization of the complex [Ru(tppz)(4,4'-(CH3)(2)bpy) Cl](+), where tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine, is reported. The ion was obtained in a one pot synthesis by reduction of Ru(4,4'-(CH3)(2)bpy) Cl-4 with triethylamine in the presence of tppz, and isolated as the hexafluorophosphate salt. The structure of [Ru(tppz)(4,4'-(CH3)(2)bpy)Cl](PF6), 1, was established by X-ray diffraction. The ruthenium atom is in a highly distorted octahedral environment with the 4,4'-(CH3)(2)bpy nitrogens, the pyrazine central nitrogen of tppz, and chlorine defining the best mean equatorial plane. The axial positions are occupied by the nitrogens of the coordinated pyridyl rings of tppz. The Ru-N(tppz) bond to the central ring is short [1.962(9) Angstrom], while the Ru-N(4,4'(CH3)(2)bpy) bond trans to it is lengthened towards a single bond distance [2.096(10) Angstrom]. This enhances the distortion in coordination of the octahedron, mainly produced by the bite angle of tppz. The distortions in 1 are evident in the H-1-NMR spectra by the shifts of characteristic resonances upheld and downfield relative to the ligand.
引用
收藏
页码:2035 / 2040
页数:6
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