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Polymeric Copper(II) Paddlewheel Carboxylate: Structural Description, Electrochemistry, and DNA‐binding Studies
Author(s) -
Iqbal Muhammad,
Ali Sqib,
Tahir Muhammad Nawaz
Publication year - 2018
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.201700375
Subject(s) - carboxylate , copper , binding constant , crystallography , electrochemistry , cyclic voltammetry , chemistry , aqueous solution , ligand (biochemistry) , electron paramagnetic resonance , square pyramid , square pyramidal molecular geometry , crystal structure , stereochemistry , binding site , nuclear magnetic resonance , organic chemistry , biochemistry , physics , receptor , electrode
A polymeric complex of copper(II) was isolated and purified from the self‐assembly of CuSO 4 and 2‐phenyl acetate in aqueous medium. It was characterized through FT‐IR, UV/Vis, electron spin resonance, electrochemical solution studies, and powder and single crystal XRD techniques. The structure was revealed to consist of directly interconnected dimeric paddlewheel building units without any intervening ligand. This type of polymeric paddlewheel structures are found very rarely. Each copper is lying in a CuO 5 square pyramid coordinated by four oxygen atoms in the square base while the axial oxygen belongs to the neighboring paddlewheel. Purity and uniform crystalline nature of the complex was assessed from matching theoretical and experimental powder XRD spectra. ESR spectrum consisted of a broad signal with g value = 2.2427, whereas electrochemical studies revealed diffusion controlled electron transfer processes with diffusion co‐efficient = 1.628 × 10 –7 cm 2 · s –1 . The results of spectroscopic techniques support each other. The complex afforded mixed binding mode with DNA yielding DNA‐binding constant values of 1.384 × 10 4 m –1 and 8.845 × 10 4 m –1 using absorption spectroscopy and cyclic voltammetry, respectively. The complex also exhibited significant activity against anti‐fungal strain Helminthosporium solani by inhibiting its 75 % ± 2.5 growth. The preliminary studies heralded excellent biological potential of the synthesized complex.