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authors |
Siegel, R; Domingues, E; De Sousa, R; Jerome, F; Morais, CM; Bion, N; Ferreira, P; Mafra, L |
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nationality |
International |
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journal |
JOURNAL OF MATERIALS CHEMISTRY |
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keywords |
MOLECULAR-SCALE PERIODICITY; ORGANIC-REACTIONS; SILICA; WATER; ORGANOSILICAS; SBA-15; WALLS |
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abstract |
Propylsulfonic acid-functionalized periodic mesoporous benzenesilica (Ph-PMO-SO3H, 1) has been shown to be exceptional solid catalysts in the acid-catalyzed condensation of indole on benzaldehyde. The reasons for this distinct behavior are so far not completely understood. Here, we present a study involving the combination of advanced high-resolution solid state magic-angle spinning (MAS) NMR characterization with the results of the application of hydrated and dehydrated 1 with different acid loadings in the acid-catalyzed condensation of indole on benzaldehyde attempting an explanation of the higher performance of these materials when compared with the conventional solid catalysts. H-1 MAS NMR investigations show the displacement of the propylsulfonic -SO3H protons to higher H-1 chemical shifts with increase of the sulfonic acid strength suggesting the formation of hydrogen bonds involving neighboring -SO3H groups. The acid strength of 1 is lowered by the presence of water. At low sulfonic acid loading the catalytic activity is surprisingly high and independent of the water presence. The 2D H-1-H-1 recoupling MAS NMR experiments indicate that the phenyl rings may protect the acidic sites against water solvation, thus affording a plausible explanation for the negligible effect of water on the catalytic activity of 1 with low acid loading. For a proton loading higher than 0.40 mmol g(-1), we observed a linear relationship between the catalyst TOF and the chemical shift value of the -SO3H proton, thus showing that solid H-1 NMR appears to be a convenient tool to predict the catalytic activity of 1 in water. |
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publisher |
ROYAL SOC CHEMISTRY |
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issn |
0959-9428 |
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year published |
2012 |
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volume |
22 |
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issue |
15 |
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beginning page |
7412 |
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ending page |
7419 |
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digital object identifier (doi) |
10.1039/c2jm15015h |
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web of science category |
Chemistry, Physical; Materials Science, Multidisciplinary |
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subject category |
Chemistry; Materials Science |
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unique article identifier |
WOS:000301957300043
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