The reactivity and catalysis at axial sites of [Ru–Ru] bonded compounds are described. Effect of axial donor at axial site of a [Ru–Ru] single bond, having electronic configuration σ2π4δ2δ*2π*4, is examined. It is shown that the stronger donor leads to longer metal–metal distances. The C–H bond activation and C–C bond formation are studied at axial site of a [Ru2(CO)4]2+ core. Metal–metal and metal–ligand cooperation is exploited for catalytic alcohol dehydrogenation to aldehyde and subsequent coupling with amine to access imine selectively. Catalytic carbene transfer reactions are discussed for a wide range of diruthenium(I,I) compounds. Catalytic utility of metal–metal multiply bonded diruthenium(II,III) compounds for C–H amination reaction is also discussed.
CITATION STYLE
Dutta, I., Sengupta, G., & Bera, J. K. (2015). Reactivity and catalysis at sites trans to the [Ru–Ru] bond. In Topics in Organometallic Chemistry (Vol. 59, pp. 59–102). Springer Verlag. https://doi.org/10.1007/3418_2015_162
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