Crystal structure of hetero(bi- and tetra-)metallic complexes of compartmental Schiff bases uniting uranyl and transition metal (Ni2+, Cu2+) ions

被引:41
|
作者
Salmon, L [1 ]
Thuéry, P [1 ]
Ephritikhine, M [1 ]
机构
[1] CEA Saclay, DSM, DRECAM, SCM,CNRS URA 331, F-91191 Gif Sur Yvette, France
关键词
Schiff bases; heteropolymetallic complexes; uranyl ions; crystal structures;
D O I
10.1016/S0277-5387(03)00366-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The first crystal structures of hetero(bi- and tetra-)metallic uranyl/3d metal ion complexes with hexadentate Schiff bases are reported. The two Schiff bases N,N'-bis(3-hydroxysalicylidene)-1,3-propanediamine (H4L-1) and N,N'-bis(3-hydroxysalicylidene)-2-methyl-1,2-propanediamine (H4L2) have been used. Both ligands complex the 3d metal ion (Ni2+ or Cu2+) in the inner N2O2 coordination site, with n additional axial pyridine ligands (0 less than or equal to n less than or equal to 2) and the uranyl ion in the outer O-4 cavity. In order to match the usual pentagonal bipyramidal geometry, the coordination sphere of the uranyl ion is completed by either a chlorine atom, giving the binuclear complex [Ni(py)(2)(L-1)UO2Cl][Hpy], or by a water molecule, resulting in the hydrogen bonded binuclear dimer [Ni(L-2)UO2(H2O)](2) or by a phenoxide oxygen atom of a second Schiff base in the tetranuclear [Cu(py)(L-1)UO2](2) species. (C) 2003 Elsevier Ltd. All rights reserved.
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页码:2683 / 2688
页数:6
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