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dc.contributor.authorSaghatforoush, L
dc.contributor.authorAdil, K
dc.contributor.authorHasanzadeh, M
dc.contributor.authorAminkhani, A
dc.contributor.authorSafarinezhad, S
dc.date.accessioned2018-08-26T09:37:29Z
dc.date.available2018-08-26T09:37:29Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58109
dc.description.abstractA simple synthetic procedure has been used to prepare two new nickel(II) complexes [Ni 2(ttpy) 2(SCN) 4], (1) and [Ni(ttpy) 2](CH 3OH) 2 (21), (2) from 4?-p-tolyl-2,2?:6?,2?-terpyridine (ttpy) ligand, potassium thiocyanate, and potassium iodide in good yields. The single crystal X-ray analyses reveal that the metals in these complexes are sixfold coordinated with M:L ratio of 1:1 and 1:2 for (1) and (2), respectively. In both complexes, the Ni(II) has distorted octahedral geometry including N 5S and N 6 environments. Versatile interactions in supramolecular level containing coordinative bonding, I···H, and N···H hydrogen bonding, ?-? stacking play considerable roles in forming crystal packing of (1) and (2). From obtained data it is concluded that differences in coordination abilities, of used counterions, cause the formation of complexes with 1:1 or 1:2 ratio of metal and ligand. Electrochemical behaviors of the both complexes were investigated.
dc.language.isoEnglish
dc.relation.ispartofActa Chimica Slovenica
dc.titleSynthesis, crystal structure and electrochemical behavior of two new ni-based complexes: [Ni 2(ttpy) 2(SCN) 4] and [Ni(ttpy) 2](CH 3OH) 2 (2I)
dc.typeArticle
dc.citation.volume59
dc.citation.issue2
dc.citation.spage322
dc.citation.epage330
dc.citation.indexScopus


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