The homogeneous hydrogenation of carbon dioxide into formate anion has been
investigated in aqueous solution, using water soluble ruthenium(II)-phosph
ine (meta-monosulphonated triphenylphosphine, TPPMS; and 1,3,5-triaza-7-pho
sphaadamantane, PTA) complexes as catalysts. These reactions take place in
amine free medium under mild conditions, bicarbonate anion is more active t
han carbon dioxide in the reduction. The initial turnover frequency of the
reduction increases with increasing H-2 pressure, as it was observed in sit
u by C-13 and H-1 NMR spectroscopy. High pressure FT-IR were used to find e
vidence for the formation of the catalytically active ruthenium hydride spe
cies.