Liu Lei-Lei, Yu Cai-Xia, Ma Feng-Ji, Li Ya-Ru, Han Jing-Jing, Lin Lu, Ma Lu-Fang
College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, Henan, P. R. China.
Dalton Trans. 2015 Jan 28;44(4):1636-45. doi: 10.1039/c4dt03271c.
Hydrothermal reactions of Cd(OAc)2·2H2O with a flexible V-shaped bipyridyl benzene ligand and five benzenedicarboxylic acid derivatives gave rise to five new coordination polymers i.e., [Cd(1,4-BDC)(bpmb)(H2O)]n (1), {[Cd(1,3-BDC)(bpmb)]·0.125H2O}n (2), [Cd2(5-Me-1,3-BDC)2(bpmb)2]n (3), [Cd(5-NO2-1,3-BDC)(bpmb)(H2O)]n (4) and [Cd(5-OH-1,3-BDC)(bpmb)(H2O)]n (5) (bpmb = 1,3-bis(pyridine-3-ylmethoxy)benzene, 1,4-H2BDC = 1,4-benzenedicarboxylic acid, 1,3-H2BDC = 1,3-benzenedicarboxylic acid, 5-Me-1,3-H2BDC = 5-methyl-1,3-benzenedicarboxylic acid, 5-NO2-1,3-H2BDC = 5-nitro-1,3-benzenedicarboxylic acid, 5-OH-1,3-H2BDC = 5-hydroxy-1,3-benzenedicarboxylic acid). Their structures have been determined by single-crystal X-ray diffraction analyses, elemental analyses, IR spectra, powder X-ray diffraction (PXRD) and thermogravimetric analyses (TGA). Compound 1 is a two-fold interpenetrating network showing the coexistence of polyrotaxane and polycatenane characters. Compounds 2 and 3 exhibit similar 2D (3,5)-connected (4(2)·6(7)·8)(4(2)·6) nets in which the bpmb ligands work as lockers in interlocking 1D [Cd(1,3-BDC/5-Me-1,3-BDC)]n chains. Compound 4 shows a 2D 4-connected (6(6)) sandwich-like structure with differently oriented [Cd(5-NO2-1,3-BDC)]n chains. Compound 5 is a 3D supramolecular pcu net based on a 1D ladder-shaped chain. These results suggest that the substituted positions of carboxylate groups and changes in substituted R groups in the 5-position of BDC ligands have significant effect on the final structures. These compounds exhibited relatively good photocatalytic activity towards the degradation of methylene blue (MB) in aqueous solution under UV irradiation. Moreover, solid-state photoluminescence properties of 1-5 were also investigated.
醋酸镉二水合物(Cd(OAc)₂·2H₂O)与一种柔性V形联吡啶基苯配体以及五种苯二甲酸衍生物发生水热反应,生成了五种新型配位聚合物,即[Cd(1,4-BDC)(bpmb)(H₂O)]ₙ(1)、{[Cd(1,3-BDC)(bpmb)]·0.125H₂O}ₙ(2)、[Cd₂(5-Me-1,3-BDC)₂(bpmb)₂]ₙ(3)、[Cd(5-NO₂-1,3-BDC)(bpmb)(H₂O)]ₙ(4)和[Cd(5-OH-1,3-BDC)(bpmb)(H₂O)]ₙ(5)(bpmb = 1,3-双(吡啶-3-基甲氧基)苯,1,4-H₂BDC = 1,4-苯二甲酸,1,3-H₂BDC = 1,3-苯二甲酸,5-Me-1,3-H₂BDC = 5-甲基-1,3-苯二甲酸,5-NO₂-1,3-H₂BDC = 5-硝基-1,3-苯二甲酸,5-OH-1,3-H₂BDC = 5-羟基-1,3-苯二甲酸)。通过单晶X射线衍射分析、元素分析、红外光谱、粉末X射线衍射(PXRD)和热重分析(TGA)确定了它们的结构。化合物1是一种具有聚轮烷和聚索烃特征共存的二重互穿网络。化合物2和3表现出相似的二维(3,5)连接(4(²)·6(⁷)·8)(4(²)·6)网络,其中bpmb配体在互锁的一维[Cd(1,3-BDC/5-Me-1,3-BDC)]ₙ链中起锁定作用。化合物4显示出具有不同取向的[Cd(5-NO₂-1,3-BDC)]ₙ链的二维4连接(6(⁶))三明治状结构。化合物5是基于一维梯形链的三维超分子pcu网络。这些结果表明,羧酸根基团的取代位置以及BDC配体5位上取代R基团的变化对最终结构有显著影响。这些化合物在紫外光照射下对水溶液中亚甲基蓝(MB)的降解表现出相对较好的光催化活性。此外,还研究了1 - 5的固态光致发光性质。