Synthesis, DNA binding and cleavage activities of copper (II) thiocyanate complex with 4-(N,N-dimethylamino)pyridine and N,N-dimethylformamide.

Spectrochim Acta A Mol Biomol Spectrosc

State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering, Lanzhou University, Tian-shui Road 222, Lanzhou 730000, PR China.

Published: October 2011

Two novel copper(II) thiocyanate complexes with 4-(N,N-dimethylamino) pyridine and N,N-dimethylformamide (1) and with 4-(N,N-dimethylamino) pyridine (2) have been synthesized and characterized. The crystal and molecular structures of complexes 1 and 2 were determined by single-crystal X-ray diffraction. Antioxidative activity tests in vitro showed that complex 1 has significant antioxidative activity against hydroxyl free radicals from the Fenton reaction and also oxygen free radicals, which is better than standard antioxidants like vitamin C and mannitol. The interaction of complex 1 with calf thymus DNA was investigated by spectroscopic, cyclic voltammetry, and viscosity measurements. Results suggest that complex 1 can bind to DNA via partial intercalation mode. Moreover, complex 1 has been found to cleavage of plasmid DNA pBR322.

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http://dx.doi.org/10.1016/j.saa.2011.05.020DOI Listing

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Article Synopsis
  • New complexes of 2-(N,N-dimethylamino)pyridine (2-DMAP) and 4-(N,N-dimethylamino)pyridine (4-DMAP) were synthesized with chloranilic acid (CLA) and characterized using various methods including X-ray diffraction and NMR spectroscopy.
  • Both complexes demonstrated proton transfer, leading to strong hydrogen bonds, and were found to have different crystallization structures.
  • Thermal analysis indicated that the methyl groups in 4-DMAP + CLA exhibit faster motion at room temperature compared to the slower motion of CH groups in 2-DMAP + CLA due to steric effects.
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