Synthesis and crystal structure of a novel ruthenium(II) complex with in situ generated dithiobiurea ligand

被引:9
|
作者
Matesanz, Ana I. [1 ]
Hernandez, Carolina [1 ,2 ]
Perles, Josefina [3 ]
Souza, Pilar [1 ]
机构
[1] Univ Autonoma Madrid, Fac Ciencias, Dept Quim Inorgan M07, C Francisco Tomas & Valiente 7, E-28049 Madrid, Spain
[2] Univ Castilla La Mancha, Fac Ciencias Medio Ambiente, Dept Quim Inorgan Organ & Bioquim, Avd Carlos III S-N, Toledo 45071, Spain
[3] Univ Autonoma Madrid, Fac Ciencias, Serv Interdept Apoyo Invest M13, C Francisco Tomas & Valiente 7, E-28049 Madrid, Spain
关键词
2,5-Dithiobiurea; Ruthenium; Thiosemicarbazone transformation; X-ray diffraction; NSS]-donor set; CYTOTOXIC ACTIVITY; THIOSEMICARBAZONE DERIVATIVES; PALLADIUM(II); BIS(THIOSEMICARBAZONES); CATALYSIS; EFFICIENT; BINDING; SERIES; CELLS;
D O I
10.1016/j.jorganchem.2015.12.035
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Upon reaction with RuCl2(PPh3)(3) in toluene in presence of triethylamine, 2,6-diacetylpyridine mono(4-methoxyphenyl thiosemicarbazone) undergoes an unusual and interesting chemical transformation leading to the formation of a dithiobiurea ruthenium(II) complex. The new complex was characterized by analytical, spectroscopic and single crystal X-ray diffraction techniques. The crystallographic study confirmed the presence of 1,6-(4-metoxyphenyl)-2,5-dithiobiurea acting as monoanionic SNS tridentate ligand. Thus the coordination geometry around the ruthenium(II) ion is a distorted octahedral where the SNS donor set of the ligand and one co-ordinated chlorido constitute the equatorial plane. The remaining apical coordination positions are filled up by two triphenylphosphines. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 17
页数:5
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