RESUMO
A series of Ru(II) and Os(II) tris-chelate complexes with new bidentate 2-pyridylquinoline ligands have been synthesized and fully characterized by EA,1H-NMR and FAB-MS techniques. The new ligands are: L1 = 4-p-methoxyphenyl-6-bromo-2-(2'- pyridyl)quinoline (mphbr-pq) and L2 = 4-p-hydroxyphenyl-6-bromo-2-(2'-pyridyl)-quinoline (hphbr-pq). The complexes studied are: [Ru(bpy)2L1](PF6)2 (C1), [Ru(bpy)2L2](PF6)2 (C2), [Os(bpy)2L1](PF6)2 (C3), [Os(bpy)2L2](PF6)2 (C4) (bpy = 2,2'-bipyridine), [Ru(dmbpy)2L1](PF6)2 (C5), [Ru(dmbpy)2L2](PF6)2 (C6), [Os(dmbpy)2L1](PF6)2 (C7), and [Os(dmbpy)2L2](PF6)2 (C8) (dmbpy = 4,4'-dimethyl-2,2'-bipyridine). Moreover, new functionalized complexes C9-C12 were obtained by the base-catalyzed direct alkylation of C2, C4, C6, and C8 with 6-bromo-1-hexene. The complete assignment of the 1H-NMR spectra for the two new ligands (L1 and L2), and their Ru(II) or Os(II) complexes has been accomplished using a combination of one- and two-dimensional NMR techniques. The JH,H values have been determined for the majority of the resonances.
Assuntos
Espectroscopia de Ressonância Magnética/métodos , Compostos de Ósmio/química , Quinolinas/química , Compostos de Rutênio/química , Ligantes , Espectrometria de Massas de Bombardeamento Rápido de ÁtomosRESUMO
Two novel bis-terdentate Ir(III)-cyclometalated complexes, [Ir(L1)(L1(-))](2+) (1) and [Ir(L1(-))(2)](+) (2), have been prepared (L1 is 2,6-bis(7'-methyl-4'-phenyl-2'-quinolyl)pyridine; L1(-) is its mono-anion, see Figure 1). To the best of our knowledge, 1 and 2 are the first luminescent and redox-active Ir(III)-cyclometalated bis-terdentate compounds. In acetonitrile solution, on oxidation, 2undergoes a reversible, metal-centered, one-electron oxidation at +1.40 V, whereas 1 does not exhibit any oxidation process up to +2.00 V. On reduction, both compounds undergo four reversible ligand-centered one-electron processes. The absorption spectra of the compounds are dominated by moderately intense (epsilon in the 10(3)-10(4) M(-)(1) cm(-)(1) range) spin-allowed metal-to-ligand charge-transfer (MLCT) bands at wavelengths longer than 350 nm and by intense (epsilon in the 10(4)-10(5) M(-)(1) cm(-)(1) range) ligand-centered (LC) bands at shorter wavelengths. The complexes exhibit an intense luminescence both at 77 K in MeOH/EtOH, 4:1 (v/v), rigid matrix (1, lambda(max) = 592 nm, tau = 20 &mgr;s; 2, lambda(max) = 598 nm, tau = 9 &mgr;s) and at room temperature in deoxygenated acetonitrile solution (1, lambda(max) = 620 nm, tau = 325 ns, Phi = 0.005; 2, lambda(max) = 630 nm, tau = 2.3 &mgr;s, Phi = 0.066). In all cases, the emission is assigned to triplet MLCT levels (namely, Ir --> L1 and Ir --> L1(-) in 1 and 2, respectively).