Ruthenium complexes alkylated clusters

Non-ionic thiourea derivatives have been used as ligands for metal complexes [63,64] as well as anionic thioureas and, in both cases, coordination in metal clusters has also been described [65,66]. Examples of mononuclear complexes of simple alkyl- or aryl-substituted thiourea monoanions, containing N,S-chelating ligands (Scheme 11), have been reported for rhodium(III) [67,68], iridium and many other transition metals, such as chromium(III), technetium(III), rhenium(V), aluminium, ruthenium, osmium, platinum [69] and palladium [70]. Many complexes with N,S-chelating monothioureas were prepared with two triphenylphosphines as substituents. 

It has been several decades since oxo-centered triruthenium-carboxylate complexes with triangular cluster frameworks of Ru3(p3-0)(p-00CR)6 (R = alkyl or aryl) were first isolated [1,2]. In the early 1970s, the first oxo-centered triruthenium complex was structurally characterized by Cotton through X-ray crystal structural determination [3]. Since then, oxo-centered trinuclear ruthenium-carboxylate cluster complexes with general formula [Ru30(00CR)6(L)2L ]n+ (R = aryl or alkyl, L and... 

However, only alkyl formates are formed in the conventional reactions of alcohols, CO2 and H2 using transition metal complexes, because intermediary hydride complexes generally react with CO2 to give formate complexes. On the other hand, we have found that mthenium cluster anions effectively catalyze the hydrogenation of CO2 to CO, methanol, and methane without forming formate derivatives [2-4]. Ethanol was also directly formed from CO2 and H2 with ruthenium-cobalt bimetallic catalyst [5]. In this paper, we report that this bimetallic catalytic... 

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