Immobilization of pyrene - adorned N - heterocyclic carbene complexes of rhodium (I) on reduced graphene oxide and study of catalytic activity
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Immobilization of pyrene - adorned N - heterocyclic carbene complexes of rhodium (I) on reduced graphene oxide and study of catalytic activityData de publicació
2018-04-24Editor
WileyCita bibliogràfica
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. 1874-1881Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
https://onlinelibrary.wiley.com/doi/epdf/10.1002/cctc.201701277Versió
info:eu-repo/semantics/acceptedVersionParaules clau / Matèries
Resum
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)Drets d'accés
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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