Synthesis, characterization and electrochemical investigations of mixed-ligand copper(II)-organic supramolecular frameworks

被引:3
|
作者
Singh, Sandeep K. [1 ,2 ]
Srivastava, Ashish Kumar [2 ]
Srivastava, Krishna [2 ]
Banerjee, Rahul [3 ]
Prasad, Jagdish [2 ]
机构
[1] UP Jal Nigam, Reg Water Anal & Res Lab, Varanasi 221005, Uttar Pradesh, India
[2] Univ Allahabad, Dept Chem, Nanosci & Electrochem Res Lab, Allahabad 211002, Uttar Pradesh, India
[3] Natl Chem Lab, Div Phys Chem, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
关键词
Mixed-ligand complex; Supramolecular framework; X-ray diffraction; Cyclic voltammetry; 5,5 '-dimethyl-2,2 '-bipyridine; pi-pi stacking interaction; METAL-ORGANIC FRAMEWORK; COORDINATION-COMPOUNDS; CRYSTAL-STRUCTURES; STRUCTURAL DATA; MAGNETIC-PROPERTIES; BENZENE-1,3,5-TRICARBOXYLIC ACID; TERNARE KOMPLEXE; CLASSIFICATION; COMPLEXES; CHEMISTRY;
D O I
10.1016/j.molstruc.2017.06.128
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two mixed-ligand copper(II)-organic coordination compounds with 5,5'-dimethyl-2,2'-bipyridine (5,5'-Me(2)bpy) as a primary ligand while aliphatic malonate (Hmal) and aromatic 2-hydroxynicotinate (2-OHNA) as secondary ligands, were synthesized. These complexes are formulated as: [Cu(Hmal)(5,5'-Me(2)bPY)(H2O)](ClO4) 1 and [Cu-2(2-OHNA)(2)(5,5'-Me(2)bpy)(2)(NO3)KNO3) 2. These two complexes were structurally characterized by single crystal X-ray diffraction analysis. Characterization was further supported by powder X-ray diffraction analysis, elemental analyses, FT-IR, FAB-MASS and TGA, DSC studies. Cyclic voltammetric and UV-visible spectral studies of these two complexes have also been done. The electrochemical studies of complex 1 in DMSO and DMF have shown that this complex undergoes quasi reversible diffusion-controlled one-electron transfer reaction without any chemical complication while complex 2 in DMSO undergoes quasi-reversible diffusion-controlled one electron transfer reaction, following EC mechanism. The electrochemical behaviour of complex 2 in DMF is complicated probably due to presence of more than one species in solution phase. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:549 / 557
页数:9
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