Spontaneous reduction of gold(III) to gold(I) by forming sulfur-bridged polynuclear structure with octahedral tris(thiolato) complexes

被引:7
作者
Konno, T [1 ]
Tokuda, K [1 ]
Abe, T [1 ]
Hirotsu, M [1 ]
机构
[1] Gunma Univ, Fac Engn, Dept Chem, Kiryu, Gumma 3768515, Japan
来源
MOLECULAR CRYSTALS AND LIQUID CRYSTALS | 2000年 / 342卷
关键词
rhodium(III); gold(I); S-bridged polynuclear complex;
D O I
10.1080/10587250008038242
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction of fac(S)-[Rh-III(aet)(3)] (aet = 2-aminoethanethiolate) with [(AuCl4)-Cl-III](-) in water gave an S-bridged pentanuclear complex [Au-3(I){Rh-III(aet)(3)}(2)](3+) (1), accompanied by the spontaneous reduction of Au-III to Au-I. The crystal structure of 1(NO3)(3). 4H(2)O was deter mined by X-ray. crystallography. In 1 two octahedral fac(S)-[Rh(aet)(3)] units are linked by three linear Au-I atoms to form a trigonal-bipyramid-type (Rh2Au3I)-Au-III pentanuclear structure with an averaged Au-I-Au-I distance of 3.083(5) Angstrom. The two (Rh2Au3I)-Au-III each other through one Au-I-Au-I interaction with a distance of 3.311(3) Angstrom. The optically active Delta Delta-1 was derived from Delta Delta Delta Delta-[Zn-3(OH){Rh(aet)(3)}(4)](5+) by reacting with [AuCl4](-) in water.
引用
收藏
页码:45 / 50
页数:6
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