dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniv Clermont Ferrand
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:21:48Z
dc.date.accessioned2022-10-05T16:13:19Z
dc.date.available2014-05-20T15:21:48Z
dc.date.available2022-10-05T16:13:19Z
dc.date.created2014-05-20T15:21:48Z
dc.date.issued2006-05-01
dc.identifierJournal of Physics and Chemistry of Solids. Oxford: Pergamon-Elsevier B.V., v. 67, n. 5-6, p. 973-977, 2006.
dc.identifier0022-3697
dc.identifierhttp://hdl.handle.net/11449/32909
dc.identifier10.1016/j.jpcs.2006.01.013
dc.identifierWOS:000239261500017
dc.identifier2545904877423127
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3905360
dc.description.abstractWe report the synthesis and characterization of organic-inorganic hybrid materials: Zn-2-Al-LDHs (layered double hydroxides) containing 3-(1H-pyrrol-1-yl)-propanoate and 7-(1H-pyrrol-l-yl)-heptanoate as the interlayer anions. The LDHs were synthesized by the co-precipitation method at constant pH followed by hydrothermal treatment for 72 h. The materials were characterized by PXRD, C-13 CP-MAS NMR, TGA, and ESR. The basal spacing found by PXRD technique is coincident with the formation of bilayers of the intercalated anions. The solid state C-13 NMR showed that the interlayered anions remain identical after intercalation. ESR data suggest that the monomers connect each other in a limited number of guests when a thermal treatment is applied. The inorganic LDH sheets delay the temperature of degradation of the monomers. (c) 2006 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationJournal of Physics and Chemistry of Solids
dc.relation2.207
dc.relation0,594
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectnanostructures
dc.subjectpolymers
dc.subjectX-ray diffraction
dc.subjectnuclear magnetic resonance (NMR)
dc.subjectelectron paramagnetic resonance (EPR)
dc.titleNew layered double hydroxides intercalated with substituted pyrroles. 2. 3-(Pyrrol-1-yl)-propanoate and 7-(pyrrol-1-yl)-heptanoate LDHs
dc.typeArtigo


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