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Syntheses, Structures and Electrochemical Properties of Two New Copper(II) Complexes Based on Isomeric Bis(pyridylformyl)piperazine Ligands and Rigid=Flexible Organic Dicarboxylates
| Content Provider | Semantic Scholar |
|---|---|
| Author | Lin, Hong-Yan Liu, Peng Wang, Xiu-Li Xu, Chuang Liu, Guo-Cheng |
| Copyright Year | 2013 |
| Abstract | Two new copper(II) complexes, [Cu2(3-bpfp)(2,6-PDA)2(H2O)2] (1) and [Cu(4-bpfp)0:5 (glu)]·H2O (2), have been hydrothermally synthesized by self-assembly of isomeric bis(pyridylformyl)piperazine ligands [3-bpfp=bis(3-pyridylformyl)piperazine, 4-bpfp=bis(4- pyridylformyl)piperazine], rigid pyridine-2,6-dicarboxylic acid (2,6-H2PDA) or flexible glutaric acid (H2glu), and copper(II) chloride. Single-crystal X-ray diffraction analysis reveals that two adjacent CuII ions are connected by the 3-bpfp ligand to build a dinuclear unit in complex 1, in which 2,6-PDA serves as a terminal chelating ligand. Adjacent dinuclear units are further linked by hydrogen bonding and π-π stacking interactions to form a three-dimensional (3D) supramolecular network. Complex 2 is a 3D coordination polymeric framework based on a layer polymer [Cu(glu)]n and bridging 4-bpfp ligands with 6-connected (44.610.8) topology. In 1 and 2, the ligands 3-bpfp and 4-bpfp adopt a μ2-bridging coordination mode (via ligation of pyridyl nitrogen atoms). The thermal stability and the electrochemical properties of the title complexes have been studied. Graphical Abstract Syntheses, Structures and Electrochemical Properties of Two New Copper(II) Complexes Based on Isomeric Bis(pyridylformyl)piperazine Ligands and Rigid=Flexible Organic Dicarboxylates |
| Starting Page | 138 |
| Ending Page | 146 |
| Page Count | 9 |
| File Format | PDF HTM / HTML |
| DOI | 10.5560/znb.2013-2291 |
| Volume Number | 68 |
| Alternate Webpage(s) | http://www.znaturforsch.com/s68b/s68b0138.pdf |
| Alternate Webpage(s) | https://doi.org/10.5560/znb.2013-2291 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |