dc.creatorWeiss López, Boris
dc.creatorGamboa, Consuelo
dc.creatorTracey, Alan S.
dc.date.accessioned2018-12-20T14:38:02Z
dc.date.available2018-12-20T14:38:02Z
dc.date.created2018-12-20T14:38:02Z
dc.date.issued1995
dc.identifierLangmuir, Volumen 11, Issue 12, 2018, Pages 4844-4847
dc.identifier15205827
dc.identifier07437463
dc.identifier10.1021/la00012a042
dc.identifierhttp://repositorio.uchile.cl/handle/2250/156786
dc.description.abstractDeuterium quadrupole splittings from the aromatic ring of a series of deuterium labeled n-alkylpyridinium ions with linear n-alkyl groups from Ci to Cie have been measured using 2H-NMR spectroscopy. These splittings were used to calculate the two order parameters describing the average alignment of the individual pyridinium rings, and these values were used to determine the location and preferred orientation of the ions when contained in either of the lyotropic liquid crystals of this study. Two cationic mesophases, prepared from either hexadecylpyridinium chloride or tetradecyltrimethylammonium bromide, were used as the host systems. The smaller alkylpyridinium ions (C1-C5) were found predominantely in the interstitial water. The intermediate size ions (C6 _C10), which were distributed moee effectively into the micelle, have a disruptive effect in the mesophase, probably a result of modifications in the degree of alignment of the micelle, possibly because of modifications of its inter
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceLangmuir
dc.subjectMaterials Science (all)
dc.subjectCondensed Matter Physics
dc.subjectSurfaces and Interfaces
dc.subjectSpectroscopy
dc.subjectElectrochemistry
dc.titleLocation and Average Alignment of Alkylpyridinium Ions in Cationic Nematic Lyomesophases
dc.typeArtículos de revistas


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