等结构
羧酸盐
金属有机骨架
固碳
化学
催化作用
环加成
吸附
星团(航天器)
金属
无机化学
结晶学
立体化学
晶体结构
有机化学
程序设计语言
二氧化碳
计算机科学
作者
Zhen-Xing Bian,Yong‐Zheng Zhang,Dan Bi Tian,Xiuling Zhang,Lin‐Hua Xie,Minjian Zhao,Ya-Bo Xie,Jian‐Rong Li
标识
DOI:10.1021/acs.cgd.0c01232
摘要
Cluster-based metal–organic frameworks (MOFs) supported by mixed ligands usually have unique properties due to the combined features from different ligands. In this regard, it is rather rare for carboxylate and pyrazolate ligands as “struts” to be present in one MOF. Herein, four isostructural heptanuclear Co(II)-based MOFs based on mixed carboxylate and pyrazolate ligands, [Co 7 (μ 3 -OH) 4 (BDP) 2 (IPA-X) 5 ] (BUT-127-X; X = H, OH, Br, and NH 2, respectively; BDP 2– = 1,4-benzenedipyrozolate and IPA 2– = isophthalate), were synthesized through carefully tuning the solvothermal reaction conditions. Structurally, in these MOFs, alternately connecting Co 7 (μ 3 -OH) 4 clusters with carboxylate ligands (IPA 2– -X) generate two-dimensional (2D) layers, which are further supported by the pyrazolate ligands (BDP 2– ), giving rise to the final pillared-layer frameworks with well adjustable pore surface environments. They have permanent porosity with high Brunauer–Emmett–Teller surfaces from 1030 to 1314 m 2 g –1, as well as good chemical stability. Interestingly, four Co(II) atoms in the Co 7 (μ 3 -OH) 4 cluster exhibit a five-coordinated configuration that affords open metal sites. The feature allows these MOFs to present good CO 2 adsorption performance and catalytic activity for the CO 2 fixation, where BUT-127-NH 2 gave the best catalytic performance for the cycloaddition of CO 2 with epoxides into cyclic carbonates under mild conditions (1 bar, 25 and 50 °C).
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