Imprint of free space around acid site in hollow mesoporous polymeric solid acid and application in heterogeneous acetal hydrolysis/asymmetric aldol tandem reaction

被引:14
作者
Bo, Yanan [1 ]
Wang, Xuri [1 ]
Deng, Xintao [1 ]
Ma, Xuebing [1 ]
机构
[1] Southwest Univ, Coll Chem & Chem Engn, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
Solid acid; Heterogeneous organocatalysis; Tandem reaction; Hydrolysis; Asymmetric aldol reaction; METAL-ORGANIC FRAMEWORKS; ASYMMETRIC ALDOL; NANO-BOWLS; CATALYTIC-ACTIVITY; IONIC LIQUIDS; BRONSTED ACID; L-PROLINE; ORGANOCATALYST; NANOSPHERES; SILICA;
D O I
10.1016/j.apcata.2019.117360
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tailoring free spaces around catalytic sites in a controlled way is highly attractive for improving the accessibility of reactants to catalytic sites in heterogeneous catalysis. In this paper, the free space around latent acid site (-SH) in the mesoporous shell of hollow polymeric nano-bowl was constructed through the hydrolysis of attached thiuronium/Co(OH)(2) complex and the formation/removal of Co(OH)(2) porogen in the shell. After the oxidation of -SH moiety by H2O2, the as-obtained hollow mesoporous bowl-like polymeric solid acid could be conveniently functionalized by 9-amino-(9-deoxy)cinchonidine (CDNH2) via acid-base reaction to afford multifunctional nano-bowl Poly(St/SO3H) HMOBs with 0.34 mmol g(-1) of loaded CDNH2 and 1.77 mmol g(-1) of acid capacity. In heterogeneous acetal hydrolysis/asymmetric aldol tandem reaction, Poly(St/SO3H-CDNH2) HMOBs displayed moderate to excellent catalytic performances (90-95% yields, anti/syn = 81/19-95/5 and 74-97%ee anti) for the starting benzaldehyde methyl acetals bearing electron-withdrawing substituents (R = NO2, Cl) at o, m and p-positions.
引用
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页数:9
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