| Abstract: | The interaction of rhenium hydrides ReHX(CO)(NO)(PR3)2 1 (X=H, R=Me (a), Et (b), iPr (c); X=Cl, R=Me (d)) with a series of proton donors (indole, phenols, fluorinated alcohols, trifluoroacetic acid) was studied by variable temperature IR spectroscopy. The conditions governing the hydrogen bonding ReHHX in solution and in the solid state (IR, X-ray) were elucidated. Spectroscopic and thermodynamic characteristics (−ΔH=2.3–6.1 kcal mol−1) of these hydrogen bonded complexes were obtained. IR spectral evidence that hydrogen bonding with hydride atom precedes proton transfer and the dihydrogen complex formation was found. Hydrogen bonded complex of ReH2(CO)(NO)(PMe3)2 with indole (2a–indole) and organyloxy-complex ReH(OC6H4NO2)(CO)(NO)(PMe3)2 (5a) were characterized by single-crystal X-ray diffraction. A short NHHRe (1.79(5) Å) distance was found in the 2a–indole complex, where the indole molecule lies in the plane of the Re(NO)(CO) fragment (with dihedral angle between the planes 0.01°). |
