Ruthenium vibrational spectroscopy

Monooxo and cis- and trans-6ioxo complexes of ruthenium(VI) and osmium(VI) are known, with the trans-6ioxo species being most common. In general, these complexes are all diamagnetic and are characterized by vibrational spectroscopy and/or X-ray crystallography. One intense metal-0x0 stretch is usually observed for monooxo and trans-dioxo complexes while two metal-oxo stretches, j/s(M(0)2) and J/as(M(0)2), are found for the cw-dioxo species in the IR spectra. The structural and vibrational data are listed in Table 4. 

A new class of binuclear nitrido complexes of tetravalent osmium and ruthenium is described in which the metal atoms are symmetrically bridged by a nitride ligand to give a linear M-N—M unit They have the stoichiometries M2NX8(H20)2]3 and [M2N(NH3)8Y2]3+ (M = Os, Ru X = Cl, Br Y = Cl, Br, etc.). Studies are reported on their vibrational spectra, structures, and bonding. Preliminary studies are reported also on trinuclear complexes of osmium and iridium. Finally, the use of vibrational spectroscopy in the study of metal-nitrido and metal-oxo complexes is discussed briefly. 

Mossbauer spectroscopy is one of the techniques that is relatively little used in catalysis. Nevertheless, it has yielded very useful information on a number of important catalysts, such as the iron catalyst for Fischer-Tropsch and ammonia synthesis, and the cobalt-molybdenum catalyst for hydrodesulfurization reactions. The technique is limited to those elements that exhibit the Mossbauer effect. Iron, tin, iridium, ruthenium, antimony, platinum and gold are the ones relevant for catalysis. Through the Mossbauer effect in iron, one can also obtain information on the state of cobalt. Mossbauer spectroscopy provides valuable information on oxidation states, magnetic fields, lattice symmetry and lattice vibrations. Several books on Mossbauer spectroscopy [1-3] and reviews on the application of the technique on catalysts [4—8] are available. 

Li et al. [47] fabricated SAMs of ruthenium phthalocyanine (RuPc) on a silver substrate precoated with an SAM of 4-mercaptopyridine (PySH) or l,4-bis[2-(4-pyridyl)ethenyl]-benzene (BPENB). SERS spectroscopy was used to explore the structure and orientation of the self-assembled films, and they successfully observed Raman bands due to vibrational modes of the pigment molecules in the composite films in the SERS spectra. 

The adsorption of carbon monoxide on supported ruthenium has been extensively studied by IR spectroscopy (ref. 4). General agreement exists on the presence of three IR bands. The LF band at 1990-2030 cm" is assigned to the vibration of carbon monoxide linearly bonded on ruthenium crystallites. The bands at 2080 and 2140 cm correspond to the vibrations of a multicarbonyl. In a recent investigation (ref. 5) this species was shown to be a tricarbonyl associated with Ru cations bonded directly to the support. 

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