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dc.contributor.authorMorán, María del Carmen-
dc.contributor.authorPinazo Gassol, Aurora-
dc.contributor.authorClapés Saborit, Pere-
dc.contributor.authorPérez, Laura-
dc.contributor.authorInfante, María Rosa-
dc.contributor.authorPons Pons, Ramon-
dc.date.accessioned2009-11-05T10:37:59Z-
dc.date.available2009-11-05T10:37:59Z-
dc.date.issued2004-06-22-
dc.identifier.citationJournal of Physical Chemistry B 108(30): 11080-11088 (2004)en_US
dc.identifier.issn1520-6106-
dc.identifier.urihttp://hdl.handle.net/10261/18321-
dc.description9 pages, 7 figures, 3 tables.-- Printed version published Jul 29, 2004.en_US
dc.description.abstractDilauroylglycerol arginine conjugates constitute a novel class of specific biocompatible surfactants, which can be considered analogues of partial glycerides and phospholipids. During their preparation, spontaneous intramolecular acyl-migration reactions are observed and both possible regioisomers are obtained: 1,2-dilauroyl-rac-glycero-3-(Nα-acetyl-l-arginine) (1212RAc) and 1,3-dilauroylglycero-2-(Nα-acetyl-l-arginine) (12RAc12). To study the influence of the presence of both regioisomers on the physicochemical properties, the phase behavior in the dry state of pure 1,2-dilauroyl-rac-glycero-3-(Nα-acetyl-l-arginine) and two mixtures of both regioisomers were studied by differential scanning calorimetry and small-angle X-ray diffraction complemented by polarized light microscopy. The experiments were performed for a sequence of heating, cooling and reheating scans. The results have shown that all samples investigated display thermotropic liquid crystallinity. The transition temperatures have been observed to be independent of the particular technique. The first heating scan is different from the cooling and reheating scans with respect to both thermal and structural parameters. The SAXS curves have shown the coexistence of two orders of lamellar spacing in the first heating scan. This coexistence is lost in subsequent scans. This suggests the presence of microphase separation of isomers in the lyophilized samples with miscibility after melting. The lamellar distance obtained for the third scan was used to study the molecular conformation of 1212RAc and 12RAc12 compounds.en_US
dc.description.sponsorshipThis work was supported by the CICYT under Project PPQ2000-1687-CO2-01.en_US
dc.format.extent22195 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsclosedAccessen_US
dc.subjectDiacylglycerol arginine-based surfactantsen_US
dc.subject1,2-dilauroyl-rac-glycero-3-en_US
dc.subject1212RAcen_US
dc.subject1,3-dilauroylglycero-2-en_US
dc.subject12RAc12en_US
dc.subjectPolarized Light Microscopyen_US
dc.subjectDifferential Scanning Calorimetry (DSC)en_US
dc.subjectSmall-angle X-ray scattering (SAXS)en_US
dc.titleInvestigation of the thermotropic behavior of isomer mixtures of diacyl arginine-based surfactants. Comparison of polarized light microscopy, DSC, and SAXS observationsen_US
dc.typeartículoen_US
dc.identifier.doi10.1021/jp0497108-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1021/jp0497108en_US
dc.identifier.e-issn1520-5207-
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