The binding capability of three ruthenium polypyridyl compounds of structural formula [Ru(apy)(tpy)Ln-](ClO4)(2-n) [1a-c; apy = 2,2'-azobis(pyridine), tpy = 2,2':6',2''-terpyridine, L = Cl, H2O, CH3CN] to a fragment of DNA was studied. The interaction between each of these complexes and the DNA model base 9-ethylguanine (9-EtGua) was followed by means of 1H NMR studies. Density functional theor...

The binding of carbon monoxide to iron, ruthenium, rhenium, and tungsten clusters is studied by means of infrared multiple photon dissociation spectroscopy. The CO stretching mode is used to probe the interaction of the CO molecule with the metal clusters and thereby the activation of the C–O bond. CO is found to adsorb molecularly to atop positions on iron clusters. On ruthenium and rhenium cl...

ruthenium dioxide nanoparticles (ruo2 ) with an average particle size of 50 nm are readily synthesized from rucl3.xh2o via the precipitation process in the presence of in-situ sodium octanoate as anionic surfactant. the phase composition, morphology, lattice parameters and size of nanoparticles in these products are characterized by fourier transform infrared spectroscopy (ft-ir), x-ray diffrac...

Little attention has been given to the use of ruthenium and osmium as catalysts for vapour-phase reactions. This paper shows that both these metals when supported on alumina possess signijcant activity for the hydrogenation of unsaturated hydrocarbons. In the hydrogenation of butene, butadiene and acetylene their activity is comparable with that shown by the other platinum group metals, althoug...

The synthesis of a ruthenium complex containing an N-heterocylic carbene (NHC) and a mesoionic carbene (MIC) is described wherein addition of a Brønsted acid results in protonolysis of the Ru-MIC bond to generate an extremely active metathesis catalyst. Mechanistic studies implicated a rate-determining protonation step in the generation of the metathesis-active species. The activity of the NHC/...

Recent developments in the chemistry of η3-allylruthenium(IV) complexes are due to their straightforward synthesis resulting from oxidative addition of allylic substrates to a ruthenium(II) center. Subsequent reaction with a nucleophile is the basis of their involvement in the catalytic allylic substitution reaction. We focus here on ruthenium-catalyzed substitution of allylic substrates by C-,...

We describe the selective cross coupling of methanol and 2-arylethanols using a combination of Ru-MACHO (RuHCl(PNP(Ph))CO) and Shvo's diruthenium complex as catalysts. The desired domino transformation takes place via so-called borrowing hydrogen methodology, which constitutes an ideal example of green chemistry.

The ruthenium complex bis-tetrabutylammonium cis-dithiocyanato-N,N9-bis-2,29-bipyridine-4-carboxylic acid, 49-carboxylate ruthenium(II), N-719, was found to block the dark current of dye sensitized solar cells (DSC), based on mesoporous TiO2 films deposited on a F-doped tin oxide electrode and the effect was compared to surface treatment by TiCl4 and the introduction of a compact TiO2 blocking ...

We report a novel ruthenium bis(pyrazolyl)borate scaffold that enables cooperative reduction reactivity in which boron and ruthenium centers work in concert to effect selective nitrile reduction. The pre-catalyst compound [κ(3)-(1-pz)2HB(N = CHCH3)]Ru(cymene)(+) TfO(-) (pz = pyrazolyl) was synthesized using readily-available materials through a straightforward route, thus making it an appealing...

The reaction of [(arene)RuCl2]2 (arene /C6H6, p -Me /C6H4 / i Pr, C6Me6) with p -thiocresol, 2-mercaptoethanol and p mercaptophenol in refluxing ethanol gives the tris-thiolato complexes [(arene)2Ru2(SR)3] (R /p -C6H4 /Me, CH2CH2OH, p C6H4OH) which can be isolated as the chloride salts. The remarkable selectivity of (arene)ruthenium units for SH versus OH functions reflects the affinity of ruth...