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hal.structure.identifierLaboratoire de chimie organique et organométallique [LCOO]
dc.contributor.authorTOUPANCE, Thierry
hal.structure.identifierLaboratoire de chimie organique et organométallique [LCOO]
dc.contributor.authorEL HAMZAOUI, Hicham
hal.structure.identifierLaboratoire de chimie organique et organométallique [LCOO]
dc.contributor.authorJOUSSEAUME, Bernard
hal.structure.identifierLaboratoire de chimie organique et organométallique [LCOO]
dc.contributor.authorRIAGUE, Hocine
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorSAADEDDIN, Iyad
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCAMPET, Guy
hal.structure.identifierInstitute of Material Science
dc.contributor.authorBRÖTZ, Joachim
dc.date.issued2006
dc.identifier.issn0897-4756
dc.description.abstractEnHydrolysis and condensation under acidic conditions of bis(triprop-1-ynylstannyl)p-phenylene 1, p-xylene 2, or butylene 3 precursors yielded bridged polystannoxanes in the form of xerogels after being dried under reduced pressure. The gels were amorphous and nonporous with very low specific surface areas. Thermal treatment of the xerogels in air at 400-500 C resulted in nanocrystalline nanoporous cassiterite tin dioxide materials, which have been thoroughly characterized by elemental analysis, FTIR, TGA-MS, powder XRD, and N2 adsorption porosimetry. The calcined materials consisted of a porous network of aggregated nanoparticles with a nanoporosity stemming from the interparticle space. A careful tuning of the precursor nature and the calcination conditions enabled the synthesis of materials with Brunauer-Emmet-Teller surface areas ranging from 40 to 150 m2 g-1, a mean pore size between 3.5 and 12 nm, and an average particle size of 5 to 25 nm. Starting from precursor 1 appeared to be the best strategy to obtain pure nanocrystalline tin dioxide materials with good textural properties for applications, with the p-phenylene bridge being easily removed by calcination.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enPolystannoxane
dc.subject.enGels
dc.subject.enNanoporous materials
dc.subject.enTin dioxide
dc.subject.enNanoparticles
dc.title.enBridged polystannoxane : a new route toward nanoporous tin dioxide
dc.typeArticle de revue
dc.identifier.doi10.1021/cm061964d
dc.subject.halChimie/Matériaux
bordeaux.journalChemistry of Materials
bordeaux.page6364-6372
bordeaux.volume18 (26)
bordeaux.peerReviewedoui
hal.identifierhal-00123376
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00123376v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Chemistry%20of%20Materials&rft.date=2006&rft.volume=18%20(26)&rft.spage=6364-6372&rft.epage=6364-6372&rft.eissn=0897-4756&rft.issn=0897-4756&rft.au=TOUPANCE,%20Thierry&EL%20HAMZAOUI,%20Hicham&JOUSSEAUME,%20Bernard&RIAGUE,%20Hocine&SAADEDDIN,%20Iyad&rft.genre=article


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