product, yielding phenylene-modified hybrid mesoporous ethenylenesilica (Ph-HME). The Ph-HME was then sulfonated by heating at 80 C for 3 days in concentrated H 2 SO 4 . The solid was recovered and washed in water at 80 C for 6 h. The washing treatment was repeated twice, and the final product was dried at room temperature to afford Ph±SO 3 H HME.Acid-Catalyzed Reaction: The esterification of acetic acid and pinacol±pinacolone rearrangement were employed as test reactions to examine the acid properties of the prepared samples. Esterification of acetic acid was examined in the liquid phase as follows: 0.20 g of the catalyst was evacuated at 423 K for 1 h and then added to a mixture of acetic acid (0.10 mol) and ethanol (1.0 mol). The reaction was carried out at 343 K in an Ar atmosphere, and the liquid phase was analyzed using gas chromatography with capillary columns. Pinacol± pinacolone rearrangement was performed in the liquid phase as follows: 0.20 g of the catalyst was evacuated at 423 K for 1 h and then added to pinacol (42.3 mol) without the addition of solvent. The reaction was carried out at 403 K in an Ar atmosphere, and the liquid phase was analyzed using gas chromatography with capillary columns.Measurement: Nitrogen adsorption±desorption isotherms were measured at 77 K using a Micrometrics Coulter SA-3100 system. Prior to measurement, the samples were pretreated at 423 K for 3 h under vacuum to a final pressure of 1 10 ±5 torr (1 torr = 133 Pa). The Brunauer±Emmett±Teller (BET) surface area was estimated over a relative pressure (P/P 0 ) range of 0.05±0.30. The pore size distribution was obtained from an analysis of the adsorption branch of the isotherms using the Barrett±Joyner±Halenda (BJH) method. Solid-state 13 C and 29 Si CP-MAS NMR measurements were acquired on Bruker ASX200 and ASX400 spectrometers, respectively. The Larmor frequencies for 13 C and 29 Si were 50.3 and 79.5 MHz, respectively. The experimental parameters were as follows.13 C CP-MAS NMR: 4.0 kHz spin rate, 5 s recycle delay, 2 ms contact time, and 4.0 ls p/2 pulse width.29 Si CP-MAS NMR experiment: 4.0 kHz spin rate, 5 s recycle delay, 5 ms contact time, 5.9 ls p/2 pulse width. The chemical shifts of 13 C and 29 Si spectra were expressed with respect to neat tetramethylsilane.