Liu Yuqian, Zhao Peiran, Duan Chunying, He Cheng
State Key Laboratory of Fine Chemicals, Dalian University of Technology Dalian 116024 P. R. China
RSC Adv. 2021 Oct 27;11(55):34779-34787. doi: 10.1039/d1ra06533e. eCollection 2021 Oct 25.
A novel 3D lanthanide(iii) metal-organic framework (MOF) (namely Tb-MOF), was synthesized by self-assembly from Tb(iii) ion nitrate and the rigid organic ligand Hsbdc (Hsbdc = 5,5-dioxo-5-dibenzo[,]thiophene-3,7-dicarboxylic acid), and could work as an efficient heterogeneous catalyst for the cyanosilylation of aromatic aldehydes at room temperature. The obtained Tb-MOF has been characterized and analysed in detail by single crystal X-ray diffraction, powder X-ray diffraction, thermogravimetric analysis and so on. The pores of Tb-MOF provided a microenvironment that was beneficial for the substrates to be close to the Lewis acid catalytic sites. The IR spectrogram and the fluorescence titration proved that the substrates could be activated inside the channel of Tb-MOF. The heterogeneous Tb-MOF catalyst with fine catalytic efficiency exhibited a high TON (TON = 460), and could be recycled at least three times without significantly reducing its activity.
通过硝酸铽(III)离子与刚性有机配体Hsbdc(Hsbdc = 5,5-二氧代-5-二苯并[,]噻吩-3,7-二羧酸)自组装合成了一种新型三维镧系(III)金属有机框架(MOF)(即Tb-MOF),其在室温下可作为芳香醛氰基硅烷化反应的高效非均相催化剂。通过单晶X射线衍射、粉末X射线衍射、热重分析等对所得Tb-MOF进行了详细表征和分析。Tb-MOF的孔提供了一个有利于底物靠近路易斯酸催化位点的微环境。红外光谱图和荧光滴定证明底物可在Tb-MOF通道内被活化。具有良好催化效率的非均相Tb-MOF催化剂表现出高TON(TON = 460),并且可以循环至少三次而不会显著降低其活性。