3.9 Article

Two New 3D Zn(II)/Cu(II) Coordination Polymers Based on N,N '-Di(3-pyridyl)succinamide and Two Different Aromatic Dicarboxylates: Syntheses, Crystal Structures and Properties

期刊

JOURNAL OF CHEMICAL CRYSTALLOGRAPHY
卷 45, 期 2, 页码 94-102

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10870-015-0570-6

关键词

Coordination polymer; Crystal structure; Aromatic dicarboxylate; Fluorescent property; Electrochemical behavior

资金

  1. National Natural Science Foundation of China [21171025]
  2. New Century Excellent Talents in University [NCET-09-0853]
  3. Program of Innovative Research Team in University of Liaoning Province [LT2012020]

向作者/读者索取更多资源

Two new 3D transition metal coordination polymers [Zn(1,3-BDC)(L)(0.5)] (1) and [Cu(5-AIP)(L)(0.5)] (2) [L= N, N'-di(3-pyridyl)succinamide, 1,3-H2BDC = 1,3-benzenedicarboxylic acid, 5-H(2)AIP = 5-aminoisophthalic acid] have been hydrothermally synthesized and structurally characterized by elemental analyses, IR, TG and single crystal X-ray diffraction analysis. In complex 1, two carboxyl groups with monodentate modes from two 1,3-BDC ligands connect two Zn(II) ions to form a dinuclear {Zn-2} SBUs, then the adjacent {Zn-2} SBUs are connected by two pairs of 1,3-BDC ligands and two L ligands to construct a 3D coordination network with the large square-shape grids. Finally, the complex 1 exhibits a 4-connected CdSO4 topology with the threefold interpenetrating feature. Complex 2 is a 3D coordination framework constructed by the ligands L and 5-AIP anions, which represents a binodal (3,8)-connected {4(2).6}(2){4(4).6(10).7(9).8(5)} topology. The different coordination modes of metal ions and two dicarboxylates play important roles in the formation of coordination frameworks for title complexes. In addition, the thermal stabilities, the fluorescent properties of complexes 1-2 and the electrochemical behavior of complex 2 modified carbon paste electrode have also been investigated. Graphical Abstract Two new 3D coordination polymers, [Zn(1,3-BDC)(L)(0.5)] (1) and [Cu(5-AIP)(L)(0.5)] (2), have been hydrothermally synthesized. Complex 1 represents a threefold interpenetrating CdSO4 topology, complex 2 exhibits a binodal (3,8)-connected {4(2).6}(2){4(4).6(10).7(9).8(5)} topology. The different coordination modes of metal ions and dicarboxylates play important roles in the formation of final structures for title complexes. [GRAPHICS] .

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