dc.contributor | Universidade de São Paulo (USP) | |
dc.contributor | Univ Clermont Ferrand | |
dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-20T15:21:03Z | |
dc.date.accessioned | 2022-10-05T16:08:45Z | |
dc.date.available | 2014-05-20T15:21:03Z | |
dc.date.available | 2022-10-05T16:08:45Z | |
dc.date.created | 2014-05-20T15:21:03Z | |
dc.date.issued | 2006-05-01 | |
dc.identifier | Journal of Physics and Chemistry of Solids. Oxford: Pergamon-Elsevier B.V., v. 67, n. 5-6, p. 968-972, 2006. | |
dc.identifier | 0022-3697 | |
dc.identifier | http://hdl.handle.net/11449/32236 | |
dc.identifier | 10.1016/j.jpcs.2006.01.012 | |
dc.identifier | WOS:000239261500016 | |
dc.identifier | 2545904877423127 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/3904827 | |
dc.description.abstract | The two-dimensional hybrid organic-inorganic materials Zn-2-Cr and Zn-2-Al-LDHs (Layered Double Hydroxides) containing 4-(1H-pyrrol-1yl)benzoate anions as the interlayer anions were synthesized by the co-precipitation method at constant pH followed by subsequent hydrothermal treatment for 72 h. The materials were characterized by PXRD, C-13 CP-MAS NMR, ESR, TGA, and TEM. The basal spacing found by the X-ray diffraction technique is coincident with the formation of bilayers of the intercalated anions. Solid-state C-13 NMR and ESR data strongly suggest the partial in situ polymerization of the 4-(1H-pyrrol-1yl)benzoate anions during coprecipitation. (c) 2006 Elsevier Ltd. All rights reserved. | |
dc.language | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation | Journal of Physics and Chemistry of Solids | |
dc.relation | 2.207 | |
dc.relation | 0,594 | |
dc.rights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | nanostructures | |
dc.subject | polymers | |
dc.subject | X-ray diffraction | |
dc.subject | nuclear magnetic resonance (NMR) | |
dc.subject | electron paramagnetic resonance (EPR) | |
dc.title | New layered double hydroxides intercalated with substituted pyrroles. 1. In situ polymerization of 4-(1H-pyrrol-1-yl)benzoate | |
dc.type | Artigo | |