Fluorescence and absorption spectroscopy, circular dichroism (CD) as well as viscosity experiment have been used to characterize the DNA binding of [Ho(Phen)(2)Cl(3)]·H(2)O, where phen stand for 1,10-phanathroline. This complex exhibits the marked decrease in the emission intensity and some hypochromism in UV-Vis spectrum in the presence of DNA. For characterization of the binding mode between the Ho(III) complex and DNA various procedures such as: absorption and emission titration and EB quenching experiments, viscosity measurements, CD study, iodide quenching assay, salt effect and thermodynamical investigation are used. The intrinsic binding constant of [Ho(Phen)(2)Cl(3)]·H(2)O with DNA is calculated by UV-Vis and florescence spectroscopy. The value of binding constants in 296, 299 and 303 are 1.99 ± 0.07 × 10(4), 1.07 ± 0.09 × 10(4) and 0.84 ± 0.06 × 10(4), respectively. The thermodynamic studies show that the reaction is entropically driven. The above-mentioned physical measurements indicate that the Ho(III) complex binds to fish salmon DNA, presumably via groove binding mode.

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http://dx.doi.org/10.1016/j.jphotobiol.2012.09.015DOI Listing

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