化学
超分子化学
催化作用
丙二腈
正交晶系
金属
配体(生物化学)
氢键
羧酸盐
堆积
金属有机骨架
吡啶
立体化学
结晶学
药物化学
分子
有机化学
晶体结构
生物化学
受体
吸附
作者
Kranthi Kumar Gangu,Suresh Maddila,Saratchandra Babu Mukkamala,Sreekantha B. Jonnalagadda
标识
DOI:10.1016/j.ica.2018.07.030
摘要
Abstract A cobalt based MOF, [Co(2,5-Pydc)(H2O)2].H2O (CoPy) was hydrothermally synthesized by employing 2,5-Pyridinedicarboxylic acid (2,5-Pydc) as organic strut; and its characteristics were characterized by single crystal XRD, FT-IR, TGA and fluorescent measurements. The single crystal XRD studies reveals that the compound crystallized in orthorhombic crystal system of space group P212121 with lattice parameters a = 7.3253(1) A b = 9.3906(1) A c = 13.8054(2) A. In CoPy, the central metal atom (Co2+) adopts a six coordination geometry by using the carboxylate oxygen atoms and nitrogen atom of pyridine ring of 2,5-Pydc. The compound is linked with 2,5-Pydc ligand in all three directions through hydrogen bonding and π-π stacking interactions, which further develops a supramolecular 3-dimensional assembled network. The CoPy exhibited impressive catalytic activity in the synthesis of seven tetrahydrobiphenylene-1,3-dicarbonitrile derivatives via an one-pot, three-component reaction between aromatic aldehyde, malononitrile and 3-methyl-cyclohexanon in ethanol giving excellent yields (91–96%) in 20-35 min reaction time. The Lewis acidic sites of CoPy, by Co2+ open metal sites probably ensure its catalytic performance. The eco-friendly protocol and recyclability of CoPy, with no noticeable leaching of metal ion, undoubtedly makes it an ideal catalyst.
科研通智能强力驱动
Strongly Powered by AbleSci AI