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dc.creatorOliveira, Vanessa E. de-
dc.creatorDiniz, Renata-
dc.creatorOliveira, Luiz Fernando C. de-
dc.date.accessioned2019-01-25T12:33:25Z-
dc.date.available2019-01-23-
dc.date.available2019-01-25T12:33:25Z-
dc.date.issued2009-
dc.citation.volume32pt_BR
dc.citation.issue7pt_BR
dc.citation.spage1917pt_BR
dc.citation.epage1925pt_BR
dc.identifier.doihttp://dx.doi.org/10.1590/S0100-40422009000700038pt_BR
dc.identifier.urihttps://repositorio.ufjf.br/jspui/handle/ufjf/8676-
dc.description.abstractOxocarbons ions are cyclic compounds presenting unusual electronic and vibrational properties. These molecules anions possess a high symmetry and degree of electronic delocalization, characteristics that have been discussed in several structural and spectroscopic investigations. Compounds in which one or more of the carbonyl oxygen atoms are replaced by other atoms or groups are called pseudo-oxocarbons. Compounds formed by substitution of the carbonyl groups by nitrogen groups former a new class named squaraines. Specificity the dicyanomethylene groups are interesting because of the possibility of further extension of the electronic delocalization and a new coordination site. These molecules also present interesting coordination properties which make these systems potentially useful in crystal engineering research.pt_BR
dc.description.resumo-pt_BR
dc.languageporpt_BR
dc.publisher-pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.initials-pt_BR
dc.relation.ispartofQuímica Novapt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectOxocarbonspt_BR
dc.subjectPseudo-oxocarbonspt_BR
dc.subjectSquarainespt_BR
dc.subject.cnpq-pt_BR
dc.titleOxocarbonos, pseudo-oxocarbonos e esquaraínaspt_BR
dc.title.alternativeOxocarbons, pseudo-oxocarbons and squarainespt_BR
dc.typeArtigo de Periódicopt_BR
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