Abstract:
:The reaction of the copper(II) diclofenac complex [Cu(dicl)2(H2O)2] (1) (dicl = deprotonated diclofenac (Hdicl)) with the chelating N-donor ligands ethylenediamine (en), propan-1,3-diamine (pn), unsymmetrical dimethylethylene-diamine (unsym-dmen) and N,N,N',N'-tetramethylethylene-diamine (temed) in methanol-water (4:1 v/v) yielded the novel copper(II) complexes [Cu(en)2(H2O)2](dicl)2·2H2O (2), [Cu(pn)2(H2O)2](dicl)2·2H2O (3), [Cu(unsym-dmen)2(H2O)](dicl)2·H2O (4) and [Cu(temed)(dicl)2] (5), respectively. All the synthesized complexes were characterized by spectroscopic (UV-vis, FT-IR) methods. The structures of complexes 2, 3 and 5 were unambiguously determined by single-crystal X-ray crystallography. X-ray structures of complexes clearly revealed the ionic structure of complexes 2, 3 and the covalent structure of complex 5. The geometry of complex 4 was optimized by Density Functional Theory (DFT) calculations. The ability of the complexes 1-5 to bind to calf-thymus DNA was monitored in vitro by diverse techniques (UV-vis spectroscopy, cyclic voltammetry, viscosity measurements) and via competitive studies with ethidium bromide. The interaction of complexes 1-5 with bovine serum albumin was studied in vitro by fluorescence emission spectroscopy and the corresponding binding constants were calculated. The biological behavior of complexes 1-5 was compared with previously reported Cu(II), Mn(II) and Ni(II) complexes of diclofenac.
journal_name
J Inorg Biochemjournal_title
Journal of inorganic biochemistryauthors
Kumar S,Sharma RP,Venugopalan P,Ferretti V,Perontsis S,Psomas Gdoi
10.1016/j.jinorgbio.2018.07.009subject
Has Abstractpub_date
2018-10-01 00:00:00pages
97-108eissn
0162-0134issn
1873-3344pii
S0162-0134(18)30091-6journal_volume
187pub_type
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