Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jcat.2008.04.002
DC FieldValue
dc.titleSBA-15-based polyamidoamine dendrimer tethered Wilkinson's rhodium complex for hydroformylation of styrene
dc.contributor.authorLi, P.
dc.contributor.authorKawi, S.
dc.date.accessioned2014-10-09T07:01:05Z
dc.date.available2014-10-09T07:01:05Z
dc.date.issued2008-07-01
dc.identifier.citationLi, P., Kawi, S. (2008-07-01). SBA-15-based polyamidoamine dendrimer tethered Wilkinson's rhodium complex for hydroformylation of styrene. Journal of Catalysis 257 (1) : 23-31. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jcat.2008.04.002
dc.identifier.issn00219517
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/90072
dc.description.abstractDendritic SBA-15 supported HRh(CO)(PPh3)3 catalysts were designed for liquid-phase hydroformylation of styrene. The silanols outside SBA-15 channels were passivated so that HRh(CO)(PPh3)3 complexes could be anchored mostly inside the SBA-15 channels. After passivation, PAMAM (polyamidoamine) dendrimers up to second generation were then grown inside the SBA-15 channels. Both pore size and dendrimer generation were found to influence the performance of catalysts for styrene hydroformylation, and the second-generation PAMAM was found to be optimal for these passivated dendritic SBA-15-supported rhodium catalysts. To study the effect of tethering HRh(CO)(PPh3)3 inside and outside SBA-15 mesopore channels, we also studied SBA-15-supported catalyst analogs with no passivation of external silanols. The passivated SBA-15 supported rhodium catalysts demonstrated an increase in catalytic activity and stability when the generation of supported dendrimer was increased from zeroth to second generation. © 2008.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.jcat.2008.04.002
dc.sourceScopus
dc.subjectDendrimer
dc.subjectDendritic catalysts
dc.subjectHRh(CO)(PPh3)3
dc.subjectHydroformylation
dc.subjectSBA-15
dc.subjectStyrene
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.jcat.2008.04.002
dc.description.sourcetitleJournal of Catalysis
dc.description.volume257
dc.description.issue1
dc.description.page23-31
dc.identifier.isiut000257810500004
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