Experimental and theoretical characterization of Ru(II) complexes with polypyridine and phosphine ligands

The synthesis and the experimental and theoretical characterization of ruthenium hydride complexes containing phosphorus and polypyridine ligands [RuH(CO)(N-N)(PPh3)2]+ with N-N = dppz 1, dppz-CH32 (2.1 isomer), dppz-Cl 3 (3.1 isomer), ppl 4, and 2,2′-biquinoline 5, (where dppz = dipyrido[3,2-a:2′,3′-c]phenazine), are presented. 1H NMR, 31P NMR, 13C NMR, IR-FT, UV–Vis and elemental analysis are used to characterize the complexes. Optimized molecular geometries in the gas phase at the B3LYP/LACVP(d,p) level showed a distorted octahedral structure for ruthenium, the phosphine ligands are localized in a trans position, while the polypyridine ligand, which in all the cases is planar except in 5, adopt a trans position relative to the carbon monoxide and hydride ligands. The theoretical absorption spectra (one hundred excited states) were calculated for the seven complexes by the time dependent density functional theory (TD-DFT) in the gas phase. They predicted very well the UV–Vis spectra. It was possible to identify the character of each electronic transition and the fragments of the complexes involved in it. Theoretical evidence of the substituent effect in the polypyridine ligand and of the ligand effect (dppz, biq, ppl) was found, displayed mainly in the longer wavelength band. The theoretical results showed that the properties of these complexes can be tuned with changes localized in the polypyridine ligand covalently bonded to ruthenium.

Synthesized ruthenium hydride complexes containing phosphorus and polypyridine ligands [RuH(CO)(N-N)(PPh3)2]+ showed, by quantum chemistry, a distorted octahedral structure of the metal with respect to the ligands, with the phosphine ligands in trans position. TD-DFT calculations predicted a metal-ligand to ligand charge transfer for the excited states of longer wavelength.Figure optionsDownload as PowerPoint slide