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2.1. ¡°One-pot¡± catalyst synthesis Siloxane starting materials were purchased from Gelest. Tri- block copolymer poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) P123 (4.0 g, 0.688 mmol, Mn 5800) was weighed into a Teflon bottle. Then 2.0 M HCl (120.0 mL, 240.0 mmol) and H2O (6.0 mL, 333.0 mmol) were added and stirred at 40 ◦C until the P123 was fully dis- solved. TEOS (8.2 mL, 37.8 mmol) was then added to the reaction, and the mixture was stirred at 40 ◦C for another 45 min prehydrolysis time. Then 2-(4-chlorosulfonylphenyl)- ethyltrimethoxysilane (0.65 g, 50/50 w/w solution in dichloro- methane, 1.0 mmol) was added, to allow for hydrolysis of the sulfonyl chloride, followed by 3-aminopropyltrimethoxysilane (0.19 mL, 1.0 mmol). The respective acid component was sub- stituted for the sulfonyl chloride for different acid functional- izations. This mixture was stirred at 40 ◦C for 20 h, then aged at 100 ◦C for 24 h. The mixture was then cooled to room temper- ature, and the resulting solid was filtered and rinsed repeatedly with excess H2O (4 ¡Á 500 mL), then allowed to dry overnight on an aspirating filter. The dried solid was then extracted with EtOH (400 mL per g) by refluxing in EtOH for 24 h to remove P123. The solid was again filtered and rinsed repeatedly with EtOH (4 ¡Á 500 mL), then dried overnight on the aspirator to obtain a dry white solid, which was further dried at 80 ◦C under vacuum for 24 h. ´ó¼Ò°ïæ½â´ðһϣ¬ÉÏÊöΪһƪ¹ÌÌåËá¼îË«¹¦ÄÜ´ß»¯¼ÁµÄÖÆ±¸·½·¨£¬ÏëÇë½Ìһϣ¬ËûÊÇÔÚËáÐÔÇé¿öÏÂÖÆ±¸µÄ£¬ÄÇô×îºó±íÃæµÄ¼îÐÔ°·Ó¦¸Ã»á±»¡°ÖÊ×Ó¡±»¯£¬ÄÇôÔõôȥÖÊ×Ó»¯£¬ÊDz»ÊÇÓùýÁ¿µÄË®³åÏ´¾Í¿ÉÒÔÁË£¿ |
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