Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/jspui/handle/123456789/4339
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dc.contributor.authorFrost, Ray Leslie-
dc.contributor.authorLópez, Andrés-
dc.contributor.authorCipriano, Ricardo Augusto Scholz-
dc.contributor.authorXi, Yunfei-
dc.date.accessioned2015-01-22T15:04:47Z-
dc.date.available2015-01-22T15:04:47Z-
dc.date.issued2013-
dc.identifier.citationFROST, R. l. et al. Vibrational spectroscopy of the borate mineral chambersite MnB7O13Cl - implications for the molecular structure. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, v. 120, p. 270-273, 2013. Disponível em: <http://www.sciencedirect.com/science/article/pii/S1386142513011839>. Acesso em: 07 out. 2014.pt_BR
dc.identifier.issn1386-1425-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/4339-
dc.description.abstractChambersite is a manganese borate mineral with formula: MnB7O13Cl and occurs as colorless crystals in the monoclinic pyramidal crystal system. Raman bands at 902, 920, 942 and 963 cm^-1 are assigned to the BO stretching vibration of the B7O13 units. Raman bands at 1027, 1045, 1056, 1075 and 1091 cm^-1 are attributed to the BCl in-plane bending modes. The intense infrared band at 866 cm^-1 is assigned to the trigonal borate stretching modes. The Raman band at 660 cm^-1 together with bands at 597, 642 679, 705 and 721 cm^-1 are assigned to the trigonal and tetrahedral borate bending modes. The molecular structure of a natural chambersite has been assessed using vibrational spectroscopy.pt_BR
dc.language.isoen_USpt_BR
dc.subjectBoratept_BR
dc.subjectChambersitept_BR
dc.subjectFerroelectric propertiespt_BR
dc.subjectRaman spectroscopypt_BR
dc.subjectInfrared spectroscopypt_BR
dc.titleVibrational spectroscopy of the borate mineral chambersite MnB7O13Cl - implications for the molecular structure.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.rights.licenseO periódico Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3487241178053.pt_BR
dc.identifier.doihttps://doi.org/10.1016/j.saa.2013.10.026-
Appears in Collections:DEGEO - Artigos publicados em periódicos

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