Polymorphism of the dinuclear CoIII–Schiff base complex [Co2(o-van-en)3]·4CH3CN (o-van-en is a salen-type ligand)

Reactions of Co(OH)2 with the Schiff base bis­(2-hy­droxy-3-meth­oxy­benzyl­idene)ethyl­enedi­amine, denoted H2(o-van-en), under different conditions yielded the previously reported complex aqua­[bis­(3-meth­oxy-2-oxido­benzyl­idene)ethyl­enedi­amine]­cobalt(II), [Co(C18H18N2O4)(H2O)], 1, under anae...

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Detalles Bibliográficos
Autores: Vráblová, Anna, Černák, Juraj, Falvello, Larry R., Tomás, Milagros
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2019
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/179136
Acceso en línea:http://hdl.handle.net/10261/179136
Access Level:acceso abierto
Palabra clave:Dinuclear cobalt(III)
Crystal structures
Polymorphism
Full interaction map
Schiff base ligand
Descripción
Sumario:Reactions of Co(OH)2 with the Schiff base bis­(2-hy­droxy-3-meth­oxy­benzyl­idene)ethyl­enedi­amine, denoted H2(o-van-en), under different conditions yielded the previously reported complex aqua­[bis­(3-meth­oxy-2-oxido­benzyl­idene)ethyl­enedi­amine]­cobalt(II), [Co(C18H18N2O4)(H2O)], 1, under anaerobic conditions and two polymorphs of [μ-bis­(3-meth­oxy-2-oxido­benzyl­idene)ethyl­enedi­amine]­bis­{[bis­(3-meth­oxy-2-oxido­benzyl­idene)ethyl­enedi­amine]­cobalt(III)} aceto­nitrile tetra­solvate, [Co2(C18H18N2O4)3]·4CH3CN, i.e. monoclinic 2 and triclinic 3, in the presence of air. Both novel polymorphs were chemically and spectroscopically characterized. Their crystal structures are built up of centrosymmetric dinuclear [Co2(o-van-en)3] complex mol­ecules, in which each CoIII atom is coordinated by one tetra­dentate dianionic o-van-en ligand in an uncommon bent fashion. The pseudo-­octa­hedral coordination of the CoIII atom is completed by one phenolate O and one amidic N atom of the same arm of the bridging o-van-en ligand. In addition, the asymmetric units of both polymorphs contain two aceto­nitrile solvent mol­ecules. The polymorphs differ in the packing orders of the dinuclear [Co2(o-van-en)3] complex mol­ecules, i.e. alternating ABABAB in 2 and AAA in 3. In addition, differences in the conformations, the positions of the aceto­nitrile solvent mol­ecules and the pattern of inter­molecular inter­actions were observed. Hirshfeld surface analysis permits a qualitative inspection of the differences in the inter­molecular space in the two polymorphs. A knowledge-based study employing Full Inter­action Maps was used to elucidate possible reasons for the polymorphism.