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Synthesis, structure and photocatalytic properties of coordination polymers based on pyrazole carboxylic acid ligands
CrystEngComm ( IF 2.6 ) Pub Date : 2020-09-15 , DOI: 10.1039/d0ce01054e
Chen-Lan Lin 1, 2, 3, 4 , Yan-Fei Chen 1, 2, 3, 4 , Li-Juan Qiu 1, 2, 3, 4 , Binglong Zhu 1, 2, 3, 4 , Xin Wang 1, 2, 3, 4 , Shi-Peng Luo 1, 2, 3, 4 , Wenyan Shi 4, 5, 6, 7, 8 , Ting-Hai Yang 1, 2, 3, 4 , Wu Lei 4, 8, 9, 10
Affiliation  

Three new compounds, namely, [Mn(hpcH)(H2O)2]·H2O (1), [Cd(hpcH)(DMF)(H2O)] (2), [Cu(hpcH2)2(H2O)2] (3), (hpcH3 = 5-hydroxy-1H-pyrazole-3-carboxylic acid) were solvothermally synthesized and characterized in detail. Compounds 1 and 2 are coordination polymers (CPs), exhibit two-dimensional (2D) layered structures and crystallize in monoclinic lattices with the C2/c and P21/c space groups, respectively. Compound 3 shows a 3D supramolecular structure constructed from six-coordinated mononuclear Cu2+ through hydrogen bonds and π–π stacking interactions. The hpcH3 ligand behaved in different coordinated modes in the three compounds. It lost two protons in compounds 1 and 2 and one proton in compounds 3. Furthermore, the photocatalytic degradation properties of compounds 1 and 2 were investigated. The results indicate that 1 and 2 show excellent photocatalytic activities for methylene blue (MB) under visible light. The photocatalytic degradation efficiency of 2 reached 96.7% in 90 minutes. The possible photocatalytic mechanisms displayed by CPs 1–2 for the photodegradation of MB have been addressed through the trapping experiment and theoretical calculations.

中文翻译:

基于吡唑羧酸配体的配位聚合物的合成,结构和光催化性能

三种新化合物,即[Mn(hpcH)(H 2 O)2 ]·H 2 O(1),[Cd(hpcH)(DMF)(H 2 O)](2),[Cu(hpcH 2)溶剂热合成2(H 2 O)2 ](3),(hpcH 3= 5-羟基-1 H-吡唑-3-羧酸)并详细表征。化合物12为配位聚合物(CP),具有二维(2D)分层结构,并在单斜晶格中以C 2 / cP结晶2个1 / c空间组。化合物3显示了6D配位的单核Cu 2+通过氢键和π-π堆积相互作用构造的3D超分子结构。hpcH 3配体在三种化合物中表现出不同的配位模式。它在化合物12中损失了两个质子,在化合物3中损失了一个质子。此外,研究了化合物12的光催化降解性能。结果表明12在可见光下对亚甲基蓝(MB)具有优异的光催化活性。的光催化降解效率2在90分钟内达到96.7%。通过捕获实验和理论计算已经解决了CP 1–2显示的可能的光催化机理,用于MB的光降解。
更新日期:2020-10-02
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