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dc.creatorAlmeida, K. J. de-
dc.creatorRamalho, T. C.-
dc.creatorAlves, M. C.-
dc.creatorVahtras, O.-
dc.date.accessioned2020-05-10T20:54:25Z-
dc.date.available2020-05-10T20:54:25Z-
dc.date.issued2012-07-
dc.identifier.citationALMEIDA, K. J. de et al. Theoretical insights into the visible near‐infrared absorption spectra of Bis (hexafluoroacetylacetonate) copper(II) in pyridine. International Journal of Quantum Chemistry, [S.l.], v. 112, n. 13, p. 2571-2577, July 2012. DOI: 10.1002/qua.23273.pt_BR
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/epdf/10.1002/qua.23273pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/40769-
dc.description.abstractThe density functional theory calculations were performed to investigate the specific solvent effects on the optical absorption spectrum of copper(II) hexafluoroacetylacetonate complex in pyridine. The effects of single and double coordination of pyridine molecules at axial position of bis(hexafluoroacetylacetonate) copper(II) indicate that both positions and intensities of 3d–3d electronic transitions are strongly dependent on the coordination environment around the copper(II) complex. The results indicate that the nature of the electron‐acceptor atoms in the equatorial ligands plays an important role in the number of solvent molecules in the first solvation shell of copper(II) acac systems.pt_BR
dc.languageen_USpt_BR
dc.publisherWileypt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceInternational Journal of Quantum Chemistrypt_BR
dc.subjectDFTpt_BR
dc.subjectOptical transitionspt_BR
dc.subjectCopper(II)pt_BR
dc.subjectSpectroscopypt_BR
dc.subjectDensity functional theorypt_BR
dc.titleTheoretical insights into the visible near‐infrared absorption spectra of Bis (hexafluoroacetylacetonate) copper(II) in pyridinept_BR
dc.typeArtigopt_BR
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