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用于醛的多相不对称氰基硅烷化反应的同手性双萘酚二胺锆金属有机框架材料

Homochiral BINAPDA-Zr-MOF for Heterogeneous Asymmetric Cyanosilylation of Aldehydes.

作者信息

Jin Fa-Zheng, Zhao Chen-Chen, Ma Hui-Chao, Chen Gong-Jun, Dong Yu-Bin

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education , Shandong Normal University , Jinan 250014 , People's Republic of China.

出版信息

Inorg Chem. 2019 Jul 15;58(14):9253-9259. doi: 10.1021/acs.inorgchem.9b00963. Epub 2019 Jun 24.

Abstract

A new homochiral was prepared by a new chiral organic linker of ()-4,4'-(6,6'-dichloro-2,2'-diethoxyl-[1,1'-binaphthalene]-4,4'-diyl)dibenzoic acid () and ZrCl under solvothermal conditions. Its structure was determined by Pawley refinement on the basis of the measured PXRD pattern determined for , and it showed that the obtained chiral MOF crystallized in the 2 space group with the same topological structure as that of UiO-66. The obtained can be a very active catalyst to catalyze aldehyde cyanosilylation. In addition, the chiral was a typical solid catalyst, which was proved by a hot leaching test; moreover, it could be reused at least five times without loss of its catalytic activity and enantioselectivity.

摘要

在溶剂热条件下,通过新型手性有机连接体()-4,4'-(6,6'-二氯-2,2'-二乙氧基-[1,1'-联萘]-4,4'-二基)二苯甲酸()和ZrCl制备了一种新型的同手性化合物。基于对所测PXRD图谱进行的Pawley精修确定了其结构,结果表明所得到的手性金属有机框架(MOF)在2空间群中结晶,具有与UiO-66相同的拓扑结构。所得到的化合物可以作为一种非常活跃的催化剂来催化醛的氰基硅烷化反应。此外,该手性化合物是一种典型的固体催化剂,这通过热浸出试验得到了证实;而且,它可以重复使用至少五次而不会损失其催化活性和对映选择性。

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