Journal
JOURNAL OF COORDINATION CHEMISTRY
Volume 67, Issue 22, Pages 3598-3612Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/00958972.2014.973867
Keywords
Cu(II) complex; Water soluble; Self-activation DNA cleavage; Protein binding
Categories
Funding
- National Natural Science Foundation of China [21171101, 21371103, 21471085]
- Tianjin Science Foundation [12JCYBJC13600]
- NFFTBS [J1103306]
- MOE Innovation Team of China [IRT13022]
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The synthesis and characterization of a water-soluble mononuclear Cu(II) complex, [CuLCl2]center dot 2CH(3)-CH2OH, where L = bis(2-quinolinyl methyl) benzyl-amine has been reported. L is a tridentate polyquinolinyl ligand, coordinated to Cu(II) via NNN donors. The central copper ion of 1 has N3Cl2 donor set in a distorted trigonal-bipyramidal geometry. The dimer existing in the solid state resulted from hydrogen bonds and pi-pi accumulation between two mononuclear units. The interaction of 1 with CT-DNA has been explored by absorption and emission titration methods, revealing partial intercalation between 1 and CT-DNA. Moreover, 1 could make pBR322 plasmid DNA cleaved by a self-activated oxidative process; hydroxyl radical and singlet oxygen may be the main reactive oxygen species species in the process. Complex 1 may quench the intrinsic fluorescence of bovine serum albumin in a static quenching process, which has been investigated by UV-visible and fluorescence spectroscopic methods. 1 also demonstrates potent cytotoxity against Hela cells with IC50 value of 2.84 mu M, which shows it to be a potential candidate as an anticancer metal-based drug.
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