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机构地区:[1]江苏省生物医药功能材料协同创新中心江苏省生物功能材料重点实验室南京师范大学化学与材料科学学院,南京210097
出 处:《应用化学》2014年第8期958-964,共7页Chinese Journal of Applied Chemistry
基 金:江苏高校优势学科建设工程资助项目~~
摘 要:以Keggin结构的几类杂多酸和三乙胺(TEA)为原料,通过简单的酸碱反应合成了相应杂多酸的TEA盐。并以它们作为催化剂,30%H2O2作氧化剂,在不使用长链相转移剂的条件下,研究了它们催化苯甲醇选择氧化制备苯甲醛的反应性能。结果表明,该类催化剂在苯甲醇的选择氧化反应中具有比相应杂多酸更高的催化活性或选择性。其中[TEAH]H2PW12O40为最佳催化剂,在适宜的反应条件下,该催化剂上苯甲醇转化率可达99.5%以上,苯甲醛选择性达~100%。催化剂可以被分离和循环使用多次,活性、选择性基本不变。用水作溶剂,避免了有机溶剂的使用,是一个高效、绿色的苯甲醛选择氧化体系。Several triethylamine(TEA) salts of heteropolyacids were synthesized by acid-base reaction using Keggin-type heteropolyacids and TEA as raw materials. These salts were used to catalyze the oxidation of benzyl alcohol to benzaldehyde in water with 30% aqueous hydrogen peroxide as oxidant without employment of phase transfer catalyst with long chain. These salts possess higher catalytic activities or selectivities than the corresponding acids. [TEAH]H2PW12O40 exhibits the best performance of all catalysts. Under the optimum reaction conditions, the conversion of benzyl alcohol and the selectivity of benzaldehyde is over 99.5% and - 100%, respectively, over [ TEAH] H2PW12O40. After the reaction, the catalyst can be isolated and used for next oxidation cycle, and the activity and selectivity are maintained in recycle. In view of the fact that water is used as reaction medium instead of organic solvent, this system is effective and green for selective oxidation of benzyl alcohol.
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