Catena(hexa-aqua-cobalt(II) tetra-aqua-(μ2-1,2,4,5-benzenecarboxylato-o, o') -cobalt(II) hydrate): A new symmetry for an old polymorphic phase
Author
dc.contributor.author
Atria Salas, Ana María
Author
dc.contributor.author
Garland, María Teresa
Author
dc.contributor.author
Baggio, Ricardo
Admission date
dc.date.accessioned
2018-12-20T15:10:53Z
Available date
dc.date.available
2018-12-20T15:10:53Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
Journal of the Chilean Chemical Society, Volumen 58, Issue 1, 2018, Pages 1576-1579
Identifier
dc.identifier.issn
07179707
Identifier
dc.identifier.issn
07179324
Identifier
dc.identifier.other
10.4067/S0717-97072013000100016
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/158292
Abstract
dc.description.abstract
The title cobalt complex (C10H38Co2O26) consists of [Co(H2O)4(C10H2O8)]2-n anionic chains, balanced by [(Co(H2O)6]2+ cations and eight solvato water molecules, some of which are disordered. The chains are formed by Co(H2O)4 "beads" threaded by fully deprotonated benzenecarboxylato anions binding in a stretched, trans fashion, and they are linked by H-bonds into a 2D structure. The cationic groups and solvato water molecules form a second kind of 2D arrays, "sanwiched" by the latter ones and linking the lot into a 3D structure through a very complex H-bonding interaction scheme. The structure presents a very conspicuous pseudo symmetry, and it appears to be a slight polymorphic modification of an already published isologue of identical formulation but with the higher symmetry properly attained, in a volume half as large. The slight differences between both structures seems to reside mainly in the (disordered) solvates, as suggested by the overlap of both models.