A study of the interaction with calf thymus DNA is described of a novel set of chiral ternary complex cations of general form [Ru(N4-tet)(phdi)]2+ (where N4
-tet is the chiral linear tetradentate R*R*-picchxn or R*-picchxnMe2). Individual equilibrium binding constants (KB) have been
determined from spectroscopic titrations employing the hypochromism induced in the visible
absorbance of the cations on interaction with the nucleic acid. These demonstrate both stereo- and
enantioselectivity in the binding interactions. These KB data, together with induced circular
dichroism and DNA thermal denaturation results, are all indicative of selective intercalation of the
bidentate components of the cations into the nucleobase stack of the duplex. Supportive
evidence for a secondary binding mode for the picchxn complexes is provided by the different
mutagenicity profiles obtained for related cations.
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