Syntheses, crystal structures, DNA binding, DNA cleavage, molecular docking and DFT study of Cu(II) complexes involving N2O4 donor azo Schiff base ligands

resumo

Here, we have reported three novel copper(II) complexes (1-3) involving azo Schiff base ligands. All the complexes have been well characterized using different spectroscopic tools and single crystal X-ray diffraction analysis. Structural and electronic parameters of the complexes have been justified by DFT and TDDFT computation. All the complexes showed minor groove binding to the AT-rich sequence of DNA. The binding properties of the complexes have been extensively studied, and are further supported by a molecular docking analysis. These complexes also showed H2O2-mediated DNA cleavage properties involving a hydroxyl radical. MTT assay of the complexes was performed and they were found to be cytotoxic. The intrinsic binding constants (K-b) were calculated to be 7.11 x 10(5) M-1, 8.36 x 10(5) M-1 and 10.81 x 10(5) M-1 for complexes 1-3, respectively. The complexes show interesting supramolecular architectures in the solid state mainly supported by pi-pi stacking interactions.

palavras-chave

DENSITY-FUNCTIONAL THEORY; EFFECTIVE CORE POTENTIALS; SET MODEL CHEMISTRY; COPPER(II) COMPLEXES; METAL-COMPLEXES; PHOTOLUMINESCENCE PROPERTIES; EXCITATION-ENERGIES; CHEMICAL NUCLEASES; ANTITUMOR-ACTIVITY; AZOMETHINE LIGAND

categoria

Chemistry

autores

Banerjee, S; Ghorai, P; Brandao, P; Ghosh, D; Bhuiya, S; Chattopadhyay, D; Das, S; Saha, A

nossos autores

agradecimentos

A. S. gratefully acknowledges the financial support of this work by the DST, India (Sanction No. SB/FT/CS-102/2014, dated-18.07.2015). D. G. gratefully acknowledges the financial support of this work by DST, India, vide sanction no. SB/FT/LS-444/2012.

Partilhe este projeto

Publicações similares

Usamos cookies para atividades de marketing e para lhe oferecer uma melhor experiência de navegação. Ao clicar em “Aceitar Cookies” você concorda com nossa política de cookies. Leia sobre como usamos cookies clicando em "Política de Privacidade e Cookies".