Incorporation of a tripodal ligand with a (N,O,O)-donor set into a new family of nickel and cobalt spin clusters

被引:23
作者
Alley, Kerwyn G.
Bircher, Roland
Guedel, Hans U.
Moubaraki, Boujemaa
Murray, Keith S.
Abrahams, Brendan F.
Boskovic, Colette [1 ]
机构
[1] Univ Melbourne, Sch Chem, Melbourne, Vic 3010, Australia
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[3] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
spin clusters; polynuclear complexes; nickel; cobalt; tripodal ligands; magnetochemistry;
D O I
10.1016/j.poly.2006.06.028
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of Ni(OAc)(2), NiX2 (X = Cl, Br) or CoCl2 with the proligand 2-amino-2-methyl-1,3-propanediol (ampdH(2),) affords a new family of tetranuclear complexes. The syntheses of [Ni-4(OAC)4(ampdH)(4)] (1) and [M4X4(ampdH)(4)] (M = Ni, X = Cl, 2; M = Ni, X = Br, 3; M = Co, X = Cl, 4) are reported, together with the single crystal X-ray structures of 1, 2 and 4 and the magnetochemical characterization of 1, 3 and 4. Each member of this family of complexes displays a low symmetry structure that incorporates a {M4O4} core unit based on a distorted cubane. Magnetic measurements reveal ferromagnetic exchange interactions for 1, 3 and 4. These give rise to S = 4 ground state spins for the tetranuclear Ni complexes and an anisotropic effective S' = 2 ground state for the Co complex. Crown Copyright (c) 2006 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:369 / 377
页数:9
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