Immobilization of pyrene - adorned N - heterocyclic carbene complexes of rhodium (I) on reduced graphene oxide and study of catalytic activity
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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Título
Immobilization of pyrene - adorned N - heterocyclic carbene complexes of rhodium (I) on reduced graphene oxide and study of catalytic activityFecha de publicación
2018-04-24Editor
WileyCita bibliográfica
RUIZ BOTELLA, Sheila; PERIS FAJARNÉS, Eduardo. (2018). Immobilization of pyrene - adorned N - heterocyclic carbene complexes of rhodium (I) on reduced graphene oxide and study of catalytic activity. ChemCatChem, v. 10, issue 8, p. 1874-1881Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://onlinelibrary.wiley.com/doi/epdf/10.1002/cctc.201701277Versión
info:eu-repo/semantics/acceptedVersionPalabras clave / Materias
Resumen
Twopyrene-tagged N-heterocyclic carbene (NHC) complexes of rhodium(I) wereobtained and characterized. Thetwo complexes were supported onto reduced graphene oxide (rGO), generating two new materials in which the molecular ... [+]
Twopyrene-tagged N-heterocyclic carbene (NHC) complexes of rhodium(I) wereobtained and characterized. Thetwo complexes were supported onto reduced graphene oxide (rGO), generating two new materials in which the molecular complexes are immob ilized by p–p stacking interactions onto the
surfaceofthe solid. The catalytic activity of both complexes and solid hybrid materials were studied in the 1,4-addition of phenylboronic acid to cyclohex-2-one, and in the hydrosilylation of terminal alkynes. The studies showed that for both reactions,the dimetallic complex displayed better catalytic performances than the monometallic one. This accounted for both the reactions performed in homogeneous conditions and for the reactions performed with the solid. In the case of the addition of phenylboronic acid to cyclohexanone,the solid containing the dimetallic catalystcould be effectively recycled up to five times, with negligible loss of activity,whereas the monometallic catalyst rapidlybecame inactive. In the hydrosilylation of terminal alkynes, the selectivity towards the b-(Z)-vinylsilane was improved if the immobilized dimetallic catalyst was used, although the catalyst startedtolose activity after the second run. [-]
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ChemCatChen (2018), v. 10, issue 8Proyecto de investigación
1) Financial support from MINECO of Spain (CTQ2014-51999-P) and 2) Universitat Jaume I (P11B2014- 02)Derechos de acceso
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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