Reversible five-coordinate ⇆ six-coordinate transformation in cobalt(II) complexes

被引:4
作者
Xiao, Linda [1 ]
Bhadbhade, Mohan [2 ]
Baker, Anthony T. [3 ]
机构
[1] Univ Technol Sydney, Sch Math & Phys Sci, POB 123, Broadway, NSW 2007, Australia
[2] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia
[3] La Trobe Univ, Coll Sci Hlth & Engn, Melbourne, Vic 3086, Australia
关键词
Reversible change in coordination number; Five-coordinate cobalt(II) complexes; X-ray crystal structures; Magnetic susceptibility measurements; Electronic spectra; NICKEL(II) COMPLEXES; TERPYRIDINE ANALOGS; TRIDENTATE LIGANDS; CRYSTAL-STRUCTURE; IRON(II);
D O I
10.1016/j.molstruc.2017.12.044
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 heterocyclic ligands 2,6-bis(pyrazol-1-yl)pyridine (L-1) and 2,6-bis(benzimidazol-2-yl)pyridine (L-2) and their cobalt(II) complexes were synthesized. The blue five-coordinate complex [Co(L-1)Cl-2] isolated initially from the reaction mixture rapidly absorbed water vapour from the atmosphere to yield the pink six-coordinate complex [Co(L-1)(H2O)(3)]Cl-2. This change is reversible upon desiccation or transferring [Co(L-1)(H2O)(3)]Cl-2 into acetonitrile. The five coordinate complex [Co(L-2)Cl-2], however, remains stable under similar conditions. The structures of the complexes [Co(L-1)Cl-2], [Co(L-1)(H2O)(3)]Cl-2 and [Co(L-2)Cl-2] have been determined by x-ray crystallography. The magnetic susceptibilities and the electronic spectra for [Co(L-1)Cl-2], [Co(L-2)Cl-2] and [Co(L-1)(H2O)(3)]Cl-2 are presented. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 118
页数:7
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