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dc.contributor.authorMagini, M.-
dc.contributor.authorDe Moraesa, M.-
dc.contributor.authorLichen, G.-
dc.contributor.authorPiccaluga, G.-
dc.date.accessioned2014-05-27T00:36:18Z-
dc.date.accessioned2016-10-25T18:12:01Z-
dc.date.available2014-05-27T00:36:18Z-
dc.date.available2016-10-25T18:12:01Z-
dc.date.issued1985-12-01-
dc.identifierhttp://dx.doi.org/10.1063/1.449659-
dc.identifier.citationThe Journal of Chemical Physics, v. 83, n. 11, p. 5797-5801, 1985.-
dc.identifier.issn0021-9606-
dc.identifier.urihttp://hdl.handle.net/11449/63731-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/63731-
dc.description.abstractTwo concentrated solutions of NiBr2 have been examined by x-ray diffraction. The Fourier transformed scattering data indicate inner complex formation between Ni2 + and Br- ions. Average numbers of bonded bromide ions per nickel atom have been determined for each solution and the reliability of the complexation numbers as well as of the other structural parameters has been critically examined. © 1985 American Institute of Physics.en
dc.format.extent5797-5801-
dc.language.isoeng-
dc.sourceScopus-
dc.titleComposition of the first coordination sphere of Ni2+ in concentrated aqueous NiBr2 solutions by x-ray diffractionen
dc.typeoutro-
dc.contributor.institutionCRE-Casaccia-
dc.contributor.institutionUniversità-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDivisione Chimica/TIB ENEA CRE-Casaccia, Rome-
dc.description.affiliationDipartimento di Scienze Chimiche Università, Via Ospedale 72, 09100 Cagliari-
dc.description.affiliationIstituto de Quimica UNESP, Araraquara, Sao Paulo-
dc.description.affiliationUnespIstituto de Quimica UNESP, Araraquara, Sao Paulo-
dc.identifier.doi10.1063/1.449659-
dc.rights.accessRightsAcesso restrito-
dc.identifier.file2-s2.0-36549094825.pdf-
dc.relation.ispartofThe Journal of Chemical Physics-
dc.identifier.scopus2-s2.0-36549094825-
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