Effect of ring size on coordination properties of trans-1,2-cycloalkanediamine ligands: Synthesis of dinuclear platinum(II) complexes as potential DNA cross-linkers
S. Ongeri et al., Effect of ring size on coordination properties of trans-1,2-cycloalkanediamine ligands: Synthesis of dinuclear platinum(II) complexes as potential DNA cross-linkers, INORG CHEM, 39(26), 2000, pp. 6131
The propensity of trans-1,2-cycloalkanediamines (C-3-C-6) to form rigid din
uclear complexes with platinum(II) was tested by reacting these ligands wit
h K[PtCl3(dmso)]. Whereas trans-1,2-cyclopropanediamine and trans-1,2-cyclo
butanediamine yielded dinuclear complexes in which the cycloalkane skeleton
confines the platinum centers to a distance of ca. 6 Angstrom, trans-1,2-c
ycropentanediamine and trans-1,2-cycrohexanediamine formed the chelates [Pt
Cl(cycloalkanediamine)(dmso)](+), which precipitated with [PtCl3(dmso)](-)
as counterion.