Di- and trinuclear CoII complexes of a bis-β-diketone ligand with variable conformation:: structure and magnetic studies

被引:51
作者
Aromi, Guillem
Stoeckli-Evans, Helen
Teat, Simon J.
Cano, Joan
Ribas, Joan
机构
[1] Univ Barcelona, Dept Quim Inorgan, E-08028 Barcelona, Spain
[2] Univ Neuchatel, Inst Chim, CH-2007 Neuchatel, Switzerland
[3] CCLRC Daresbury Lab, Warrington WA4 4AD, Cheshire, England
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Adv Light Source, Berkeley, CA 94720 USA
[5] ICREA, Barcelona, Spain
关键词
D O I
10.1039/b602831d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The bis-beta-diketone-phenol ligand H3L reacts with Co(OAc)(2) to become part of di- or trinuclear complexes in various conformations, depending on the nature of the co-ligand present in the reaction. Thus, the following series of complexes have been synthesized: [Co-2(HL)(2)(Solv)(4)] (Solv = py, 1; MeOH, 2), [Co-2(HL)(2)(LL)(2)] (LL = bpy, 3; bpya, 4; Ph(2)bpy, 5; phen, 6) and [Co-3(HL)(3)] ( 7), of which 1, 3, and 7 have been crystallographically characterized. The solvent-controlled interconversion between the trinuclear complex and dinuclear complexes 1 or 2 has been demonstrated. The distortion of the Co-II coordination geometry within 1, 3, and 7 has been evaluated through Continuous Shape Measures, whereas their magnetic data have been treated with models that include spin - orbit coupling effects.
引用
收藏
页码:2635 / 2644
页数:10
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