L. Maresca et al., Endocyclic versus exocyclic N-coordination to platinum(II) of some nitro-9-[(2-dialkylaminoethyl)amino]acridines, INORG CHIM, 304(2), 2000, pp. 274-282
The kinetically controlled reaction products between the antitumor drugs 1-
nitro-9-[(2-dialkylaminoethyl)amino]acridine (alkyl = Me, A(1); Et, A(2)) o
r the inactive analogs 3-nitro-9-[(2-dialkylaminoethyl)amino]acridines (alk
yl = Me, A(3); Et, A(4)) and three different platinum(II) substrates have b
een investigated in chloroform and acetone solutions and found to be depend
ent upon the charge of the metal complex and the position of the tautomeric
equilibrium (amino and imino forms) in the free acridine. Anionic ([Pt(eta
(2)-C2H4)Cl-3](-)) and neutral ([PtI2(DMSO)](2)) platinum substrates react
with the dominant tautomer, either amino or imino, to give the endocyclic a
nd exocyclic N-bonded derivatives, respectively. Positively charged substra
tes ([Pt(H2O)(Me(5)dien)](2+) and [Pt(H2O)(dien)](2+)) coordinate exclusive
ly to the exocyclic aminic nitrogens and this coordination mode stabilizes
the imino form also in the case of 3-nitro acridines, which are present in
both solvents as pure amino tautomers. For dien-platinum complexes fast exc
hange between free and coordinated acridine was observed at room temperatur
e. (C) 2000 Elsevier Science S.A. All rights reserved.