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dc.contributor.author Son, Jung Su -
dc.contributor.author Lim, Sung Chul -
dc.contributor.author Lee, Ho Chun -
dc.contributor.author Hong, Seung Tae -
dc.date.available 2017-07-11T06:11:14Z -
dc.date.created 2017-04-20 -
dc.date.issued 2015-06 -
dc.identifier.issn 2056-9890 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2956 -
dc.description.abstract In the structure of the title salt, [Co(C6H6N2)2(H2O)2](BF4)2, the CoII atom is located on an inversion centre. The transition metal is in a slightly distorted octahedral coordination environment, defined by the cyano N atoms of four hex-3-enedinitrile ligands in equatorial positions and the O atoms of two water molecules in axial positions. The bridging mode of the hex-3-enedinitrile ligands leads to the formation of cationic chains extending parallel to [110]. The BF4- counter-anion is disordered over two sets of sites [occupancy ratio = 0.512 (19):0.489 (19)]. It is located in the voids between the cationic chains and is connected to the aqua ligands of the latter through O-H⋯F hydrogen bonds. One methylene H atom of the hex-3-enedinitrile ligand forms another and weak C-H⋯O hydrogen bond with a water O atom of a neighbouring chain, thus consolidating the three-dimensional network structure. -
dc.language English -
dc.publisher International Union of Crystallography -
dc.title Crystal structure of catena-poly[[[diaquacobalt(II)]-bis(Pi-hex-3-enedinitrile-Kappa 2N:N')] bis(tetrafluoridoborate)] -
dc.type Article -
dc.identifier.doi 10.1107/S2056989015009548 -
dc.identifier.scopusid 2-s2.0-84983112924 -
dc.identifier.bibliographicCitation Acta Crystallographica Section E: Crystallographic Communications, v.71, pp.m135 - m136 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor crystal structure -
dc.subject.keywordAuthor cobalt -
dc.subject.keywordAuthor hex-3-enedinitrile -
dc.subject.keywordAuthor hydrogen bonding -
dc.subject.keywordPlus LITHIUM-ION BATTERIES -
dc.citation.endPage m136 -
dc.citation.startPage m135 -
dc.citation.title Acta Crystallographica Section E: Crystallographic Communications -
dc.citation.volume 71 -

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