Stereoselective formation of seven-coordinate titanium(IV) monomer and dimer complexes of ethylenebis(o-hydroxyphenyl)glycine

Reactions between the antitumor agent titanocene dichloride (Cp2TiCl2) and the hexadentate ligand N,N'-ethylenebis-(o-hydroxyphenylglycine) (H(4)ehpg) have been investigated in aqueous solution and the solid state. The racemi c ligands give crystals of the monomer [Ti(ehpg)(H2O)].(11/3)H2O (1), while the meso ligand gives the ore-bridged dimer [{Ti(Hehpg)(H2O)}(2)O] . 13H(2 )O (2). Complex 1 crystallizes in the monoclinic space group C2/c with a 24 .149(4) Angstrom, b = 14.143(3) Angstrom, c = 19.487(3) Angstrom, beta = 10 5.371(13)degrees, V = 6417.7(19) Angstrom(3), Z = 12, and R(F) 0.0499 for 4 428 independent reflections having I > 2 sigma(I), and contains seven-coord inate pentagonal-bipyramidal T-IV with two axial phenolate ligands (Ti-O, 1 .869(2) Angstrom). The pentagonal plane contains the two N-atoms at 2.210(2 ) Angstrom, two carboxylate O-atoms at 2.061(2) Angstrom, and a water molec ule (Ti-OH2, 2.091(3) Angstrom). Complex 2 crystallizes as an oxygen-bridge d dimer in the triclinic space group P-l with a = 12.521(6) Angstrom, b = 1 4.085(7) Angstrom, c = 16.635(8) Angstrom, alpha = 80.93(2)degrees, beta = 69.23(2)degrees, V = 64.33(2) Angstrom(3) z = 4, 72(2) Angstrom(3), Z = 4, and R(F) = 0.0580 for 5956 independent reflections having I > 2 sigma(I). E ach seven-coordinate, pentagonal-bipyramidal Ti-IV has a bridging oxide and a phenolate as axial ligands. The pentagonal plane donors are H2O, two car boxylate O-atoms, and two NH groups, which form H-bonds to O-atoms both in the same half-molecule (O ... N, 2.93-3.13 Angstrom) and in the other half- molecule (O ... N, 2.73-2.75 Angstrom); the second phenoxyl group of each H ehpg ligand is protonated and not coordinated to Ti-IV, but H-bonds to a ne arby amine proton (O ... N, 2.73-2.75 Angstrom) from the same ligand and to a nearby H2O (O ... O, 2.68 Angstrom). In contrast to ail previously repor ted crystalline metal-EHPG complexes containing racemic ligands, in which t he N(S,S)C(R,R) or N(R,R)C(S,S) form is present, complex 1 unexpectedly con tains the N(S,S)C(S,S) and N(R,R)C(R,R) forms. This is attributed to the pr esence of ring strain in seven-coordinate Ti-IV complexes. Moreover, the ra c ligands selectively form crystals of monomeric 1, while the mese ligand s electively forms crystals of the dimer 2 (N(R,R)C(R,S) or N(S,S)C(S,R)). Co mplexes 1 and 2 exhibit phenolate-to-Ti-IV charge-transfer bands near 387 n m, and 2D NMR studies indicate that the structures of 1 and 2 in solution a re similar to those in the solid state. Complex 1 is stable over the pH ran ge 1.0-7.0, while 2 is stable only between pH 2.5 and pH 5.5. Cp2TiCl2 reac ts with EHPG at pH* 7.0 to give complex 1 with a t(1/2) of ca, 50 min (298 K), but complex 2 was not formed at this pK* value. At pH* 3.7, the reactio n is very slow: 1 forms with a half-life of ca. 2.5 d, and 2 after ca. 1 we ek at ambient temperature. The relevance of these data to the possible role of serum transferrin as a mediator for the delivery of Ti-IV to tumor cell s is discussed.