TY - JOUR
T1 - Niobium-silica catalysts for the selective epoxidation of cyclic alkenes
T2 - The generation of the active site by grafting niobocene dichloride
AU - Tiozzo, Cristina
AU - Bisio, Chiara
AU - Carniato, Fabio
AU - Gallo, Alessandro
AU - Scott, Susannah L.
AU - Psaro, Rinaldo
AU - Guidotti, Matteo
PY - 2013/8/28
Y1 - 2013/8/28
N2 - Niobium-containing silica materials obtained by deposition via liquid-phase grafting or dry impregnation of niobocene(iv) dichloride are active and selective catalysts in the epoxidation of alkenes in the presence of aqueous hydrogen peroxide. The generation of the catalytically-active Nb species was followed step-by-step, and investigated using a combined DR-UV-Vis, NIR, Raman, XRD, XANES and EXAFS analyses. At the end of the grafting procedure, the nature of the surface active species can be described as an oxo-Nb(v) site, tripodally grafted onto the silica surface in close proximity to other Nb(v) centres. The liquid-phase methodology provides a better dispersion of the metal sites onto the siliceous support than the dry-impregnation approach. The niobium-silica catalysts were then tested in the epoxidation of cyclohexene and 1-methylcyclohexene, as model substrates.
AB - Niobium-containing silica materials obtained by deposition via liquid-phase grafting or dry impregnation of niobocene(iv) dichloride are active and selective catalysts in the epoxidation of alkenes in the presence of aqueous hydrogen peroxide. The generation of the catalytically-active Nb species was followed step-by-step, and investigated using a combined DR-UV-Vis, NIR, Raman, XRD, XANES and EXAFS analyses. At the end of the grafting procedure, the nature of the surface active species can be described as an oxo-Nb(v) site, tripodally grafted onto the silica surface in close proximity to other Nb(v) centres. The liquid-phase methodology provides a better dispersion of the metal sites onto the siliceous support than the dry-impregnation approach. The niobium-silica catalysts were then tested in the epoxidation of cyclohexene and 1-methylcyclohexene, as model substrates.
UR - http://www.scopus.com/inward/record.url?scp=84884343733&partnerID=8YFLogxK
U2 - 10.1039/c3cp51570b
DO - 10.1039/c3cp51570b
M3 - Article
SN - 1463-9076
VL - 15
SP - 13354
EP - 13362
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 32
ER -