TY - JOUR
T1 - The acidity and catalytic activity of supported acidic cesium dodecatungstophosphates studied by MAS, NMR, FTIR and catalytic test reaction
AU - Molnár, A.
AU - Beregszászi, T.
AU - Fudala, A.
AU - Lentz, Patrick
AU - Kónya, Z.
AU - Kiricsi, I.
A2 - B.Nagy, Janos
PY - 2001
Y1 - 2001
N2 - Acidic cesium salts of dodecatungstophosphoric acid (H3PW) supported on silica and MCM-41 were characterized by multinuclear MAS NMR, FTIR, and catalytic test reactions. 31P-NMR data indicate that the supported samples contain salts of various stoichiometries (Cs3PW and Cs2HPW) and even H3PO4. According to 29Si-NMR data, deposition of the Cs salt does not change the relative amount of various SiOH groups in the case of the silica support. In contrast, when the support is MCM-41, the relative amount of the SiOH groups increases significantly, indicating the breaking of the siloxane bonds resulting from their interaction with H3PW. The 133Cs MAS-NMR spectra also suggest that the CsPW salt interacts more strongly with the MCM-41 support than with SiO2. The results of catalytic studies show that cesium salts of dodecatungstophosphoric acid with low Cs content supported on silica or MCM-41 (Cs1.7H1.3[PW12O40]-on-SiO2 and Cs1.8H1.2[PW12O40]-on-MCM41) are active, selective, and recyclable catalysts in Friedel–Crafts alkylations (isopropylation, transalkylation), the aromatic ortho-Claisen rearrangement, and the dehydration of pinacol. The specific activity of these catalyst preparations are comparable with that of neat Cs2.6H0.4[PW12O40]. This indicates that the active species are in a well-dispersed form.
AB - Acidic cesium salts of dodecatungstophosphoric acid (H3PW) supported on silica and MCM-41 were characterized by multinuclear MAS NMR, FTIR, and catalytic test reactions. 31P-NMR data indicate that the supported samples contain salts of various stoichiometries (Cs3PW and Cs2HPW) and even H3PO4. According to 29Si-NMR data, deposition of the Cs salt does not change the relative amount of various SiOH groups in the case of the silica support. In contrast, when the support is MCM-41, the relative amount of the SiOH groups increases significantly, indicating the breaking of the siloxane bonds resulting from their interaction with H3PW. The 133Cs MAS-NMR spectra also suggest that the CsPW salt interacts more strongly with the MCM-41 support than with SiO2. The results of catalytic studies show that cesium salts of dodecatungstophosphoric acid with low Cs content supported on silica or MCM-41 (Cs1.7H1.3[PW12O40]-on-SiO2 and Cs1.8H1.2[PW12O40]-on-MCM41) are active, selective, and recyclable catalysts in Friedel–Crafts alkylations (isopropylation, transalkylation), the aromatic ortho-Claisen rearrangement, and the dehydration of pinacol. The specific activity of these catalyst preparations are comparable with that of neat Cs2.6H0.4[PW12O40]. This indicates that the active species are in a well-dispersed form.
U2 - 10.1006/jcat.2001.3285
DO - 10.1006/jcat.2001.3285
M3 - Article
SN - 0021-9517
VL - 202
SP - 379
EP - 386
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 2
ER -