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Bis{(E)-3-[(diethylmethylammonio)methyl]-N-[3-(N,N-dimethylsulfamoyl)-1-methylpyridin-4-ylidene]-4-methoxyanilinium} tetraiodide pentahydrate

dc.contributor.authorRodrigues, Tiago
dc.contributor.authorMoreira, Rui
dc.contributor.authorDacunha-Marinho, Bruno
dc.contributor.authorLopes, Francisca
dc.date.accessioned2015-12-30T10:17:41Z
dc.date.available2015-12-30T10:17:41Z
dc.date.issued2009
dc.description.abstractThe title compound, 2C(21)H(34)N(4)O(3)S(2+)center dot 4I(-)center dot 5H(2)O, was prepared exclusively as the E isomer by methylation of the corresponding N-phenylpyridin-4-amine. There are two symmetry-independent molecules in the asymmetric unit with no significant differences in bond lengths and angles. The aromatic rings are not coplanar with the pyridin-4-imine groups, as indicated by the C-N-C-C torsion angles of 47.7 (7) and 132.6 (5)degrees.. - Fundacao para a Ciencia e Tecnologia (FCT, Portugal) [SFRH/BD/30689/2006]. - Intensity measurements were performed at the Unidade de Raios X, RIAIDT, University of Santiago de Compostela, SPAIN. This work was supported by Fundacao para a Ciencia e Tecnologia (FCT, Portugal); TR acknowledges the FCT for the PhD grant SFRH/BD/30689/2006.
dc.formatapplication/pdf
dc.identifier.citationACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE. - Vol. 65, Part 2 (FEB 2009), p. O283-U1828
dc.identifier.doihttp://dx.doi.org/10.1107/S1600536809000324
dc.identifier.issn1600-5368
dc.identifier.urihttp://hdl.handle.net/10451/21197
dc.language.isoeng
dc.publisherWILEY-BLACKWELL PUBLISHING, INC
dc.subjectCrystallography
dc.titleBis{(E)-3-[(diethylmethylammonio)methyl]-N-[3-(N,N-dimethylsulfamoyl)-1-methylpyridin-4-ylidene]-4-methoxyanilinium} tetraiodide pentahydrate
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPageU1828por
oaire.citation.startPageO283por
oaire.citation.titleACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINEpor
oaire.citation.volumeVol. 65por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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