Gao Jinsuo, Zhang Xueying, Lu Yong, Liu Shaomin, Liu Jian
Key Laboratory of Industrial Ecology and Environmental Engineering (MOE), School of Environmental Science and Technology, State Key Laboratory of Fine Chemicals, Dalian University of Technology, Linggong Road 2, Dalian 116024 (P. R. China).
Chemistry. 2015 May 11;21(20):7403-7. doi: 10.1002/chem.201500532. Epub 2015 Mar 27.
The inner-surface functionalization of hollow silica spheres has rarely been reported and is still a challenging topic. Herein, we report a deacetalization-Henry cascade reaction catalyzed by dual-functionalized mesoporous silica hollow nanospheres with basic amine groups (NH2 ) on the internal shell and carboxylic acid groups (COOH) on the external shell. The selective functionalization has been realized by a combination of "step-by-step post-grafting" and "cationic surfactant-assisted selective etching" strategy. Compared to unisolated catalyst, the selectively isolated acidic and basic dual catalyst provides excellent catalytic performance for the deacetalization-Henry cascade reaction in terms of both activity (>99 %) and selectivity (95 %).
中空二氧化硅球的内表面功能化鲜有报道,仍然是一个具有挑战性的课题。在此,我们报道了一种由双功能化介孔二氧化硅空心纳米球催化的脱缩醛-Henry级联反应,该纳米球在内壳具有碱性胺基(NH2 ),在外表面具有羧酸基团(COOH)。通过“逐步后接枝”和“阳离子表面活性剂辅助选择性蚀刻”策略的组合实现了选择性功能化。与未分离的催化剂相比,选择性分离的酸性和碱性双催化剂在活性(>99%)和选择性(95%)方面都为脱缩醛-Henry级联反应提供了优异的催化性能。