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Turning over on sticky balls: preparation and catalytic studies of surface-functionalized TiO2 nanoparticles
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4614480
Author(s) Freimann, Sven A.; Prescimone, Alessandro; Housecroft, Catherine E.; Constable, Edwin C.
Author(s) at UniBasel Housecroft, Catherine
Prescimone, Alessandro
Constable, Edwin Charles
Freimann, Sven
Year 2021
Title Turning over on sticky balls: preparation and catalytic studies of surface-functionalized TiO2 nanoparticles
Journal RSC Advances
Volume 11
Number 10
Pages / Article-Number 5537-5547
Abstract We have investigated the reactivity of rhodium(III) complex-functionalized TiO2 nanoparticles and demonstrate a proof-of-principle study of their catalytic activity in an alcohol oxidation carried out under aqueous conditions water in air. TiO2 nanoparticles (NPs) have been treated with (4-([2,20:60,200- terpyridin]-40-yl)phenyl)phosphonic acid, 1, to give the functionalized NPs (1)@TiO2. Reaction between (1) @TiO2 NPs and either RhCl3$3H2O or [Rh2(m-OAc)4(H2O)2] produced the rhodium(III) complexfunctionalized NPs Rh(1)2@TiO2. The functionalized NPs were characterized using thermogravimetric analysis (TGA), matrix-assisted laser desorption ionization (MALDI) mass spectrometry, 1H NMR and FT-IR spectroscopies; the single crystal structures of [Rh(1)2][NO3]3$1.25[H3O][NO3]$2.75H2O and of a phosphonate ester derivative were determined. 1H NMR spectroscopy was used to follow the reaction kinetics and to assess the recyclability of the NP-supported catalyst. The catalytic activity of the Rh(1)2@TiO2 NPs was compared to that of a homogeneous system containing [Rh(1)2]3+, confirming that no catalytic activity was lost upon surface-binding. Rh(1)2@TiO2 NPs were able to withstand reaction temperatures of up to 100 C for 24 days without degradation.
Publisher Royal Society of Chemistry
ISSN/ISBN 2046-2069
URL https://pubs.rsc.org/is/content/articlelanding/2021/ra/d0ra09319j#!divAbstract
edoc-URL https://edoc.unibas.ch/81395/
Full Text on edoc Available
Digital Object Identifier DOI 10.1039/d0ra09319j
 
   

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