Luminescent mononuclear and binuclear cyclometalated palladium(II) complexes of 6-Phenyl-2,2'-bipyridines: Spectroscopic and structural comparisons with platinum(II) analogues 1,2

Abstract

The mononuclear cyclometalated Pd(II) complexes [Pd(L 1)X] (HL 1 = 6-phenyl-2,2'-bipyridine; X = Cl, 1a; Br, 1b; I, 1c), [Pd(L 1)PPh 3] + (1d), [Pd(L 2-5)Cl] [2a-5a, HL 2-5 = 4-(aryl)-6-phenyl-2,2'-bipyridine; aryl = phenyl (2), 4-chlorophenyl (3), 4-tolyl (4), 4-methoxyphenyl (5)] and the binuclear derivatives [Pd 2(L 1-5) 2(μ-dppm)] 2+ (1e-5e, dppm = bis(diphenylphosphino)methane) and [Pd 2(L 1) 2(μ-dppC 5)] 2+, (1f, dppC 5 = 1,5-bis(diphenylphosphino)pentane) were prepared. The crystal structures of 1d(ClO 4), 1e(ClO 4) 2·DMF, and 2e(ClO 4) 2 have been determined by X-ray crystallography. The magnitude of the Pd-Pd distances in 1e and 2e (3.230(1) and 3.320(2) Å, respectively) suggest minimal metal-metal interaction, although π-stacking of the aromatic ligands (interplanar separations 3.34 and 3.35 Å, respectively) is evident. All complexes display low-energy UV absorptions at λ ~ 390 nm, which are tentatively assigned to 1MLCT transitions; red shifts resulting from Pd-Pd interactions in the binuclear species are not apparent. The complexes in this work are non-emissive at 298 K, but the cationic derivatives exhibit intense luminescence at 77 K. The structured emissions of 1d and 1f in MeOH/EtOH glass (λ(max) 467-586 nm) and all cationic species in the solid state (λ(max) 493-578 nm) are assigned to intraligand excited states. Complexes 1e-5e display dual emissions in MeOH/EtOH glass at 77 K, and the broad structureless bands at λ(max) 626-658 nm are attributed to π-π excimeric IL transitions. A comparison between the photophysical properties of Pd(II) and Pt(II) congeners is presented.