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Magnetic properties and luminescence sensing of five coordination polymers based on a rigid terphenyl-tetracarboxylic acid
CrystEngComm ( IF 3.1 ) Pub Date : 2017-10-13 00:00:00 , DOI: 10.1039/c7ce01510k
Ling-Ling Gao 1, 2, 3, 4, 5 , Qian-Nan Zhao 1, 2, 3, 4, 5 , Miao-Miao Li 1, 2, 3, 4, 5 , Li-Ming Fan 1, 2, 3, 4, 5 , Xiao-Yan Niu 1, 2, 3, 4, 5 , Xiao-Qing Wang 1, 2, 3, 4, 5 , Tuo-Ping Hu 1, 2, 3, 4, 5
Affiliation  

Herein, five coordination polymers, namely {[Ni2(tptc)(4,4′-bibp)2]·2H2O·2cyclohexanol}n (1), {[Co2(tptc)(4,4′-bibp)2]·2H2O·2cyclohexanol}n (2), {[Zn2(tptc)(1,2-bimb)2]}n (3), {[Co(tptc)0.5(1,4-bib)]·H2O·DMF}n (4), and {[Co2(tptc)(1,2-bimb)(H2O)]·H2O}n (5) (H4tptc = terphenyl-3,3′′,5,5′′-tetracarboxylic, 4,4′-bibp = 4,4′-bis(imidazolyl)biphenyl, 1,4-bib = 1,4-bis(imidazol-1-yl)benzene, and 1,2-bimb = 1,2-bis(imidazol-1-ylmethyl)benzene) were successfully constructed based on a rigid terphenyl-tetracarboxylic acid ligand and N-containing auxiliary ligands under solvothermal conditions. Their structures were determined by single-crystal X-ray diffraction and further characterized by elemental analyses, IR spectroscopy, powder X-ray diffraction (PXRD), and thermogravimetric (TG) analyses. Complexes 1 and 2 involved a new 4,6-c 3D network structure. Complex 3 displayed an open 3D structure with the bbf topological type. Complex 4 involved an extended 3D (4,6)-c network with the point symbol of {44·610·8}{44·62}. Complex 5 had a 2D framework with the dinuclear [Co2(COO)2] SBUs. The variable-temperature magnetic susceptibilities of complexes 1, 2, 4, and 5 were also investigated, and the results indicated that the isophthalic acid bridge exhibited weak ferromagnetic coupling. Moreover, the fluorescence experiments showed that complex 3 had a potential application in the sensing of small organic molecules.

中文翻译:

五种基于刚性三联苯四甲酸的配位聚合物的磁性能和发光传感

在此,五种配位聚合物,即{[Ni 2(tptc)(4,4'-bibp)2 ]·2H 22环己醇} n1),{[Co 2(tptc)(4,4'-bibp) )2 ]·2H 22环己醇} n2),{[Zn 2(tptc)(1,2-bimb)2 ]} n3),{[Co(tptc)0.5(1,4-bib) )]·H 2 O·DMF} n4)和{[Co 2(tptc)(1,2-bimb)(H 2 O)]·H 2 O} n5)(H 4 tptc =联苯-3,3'',5,5''-四羧酸,4,4'-bibp = 4,4'-双(咪唑基)联苯,1,4-bib = 1,4-在刚性三苯基四羧酸配体和含氮辅助配体的基础上成功构建了双(咪唑-1-基)苯和1,2-bimb = 1,2-双(咪唑-1-基甲基)苯溶剂热条件。它们的结构通过单晶X射线衍射确定,并进一步通过元素分析,红外光谱,粉末X射线衍射(PXRD)和热重分析(TG)分析来表征。络合物12涉及一种新的4,6--C三维网络结构。复合体3显示了具有bbf拓扑类型的开放式3D结构。复杂4涉及一个扩展的3D(4,6)-c网络,其点符号为{4 4 ·6 10 ·8} {4 4 ·6 2 }。配合物5具有带有双核[Co 2(COO)2 ] SBU的二维框架。复合物的变温磁化率124,和5也进行了研究,结果表明,间苯二甲酸桥表现出弱的铁磁耦合。此外,荧光实验表明,配合物3在检测有机小分子方面具有潜在的应用前景。
更新日期:2017-11-13
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