We report here the synthesis of the new hydride complexes (C5H4CH(CH2CH2)(2
)NMe)RuH(PPh3)(2) (1) and [(C5H4CH(CH2CH2)(2)NHMe)-RuH(PPh3)(2)] (BF4) (2),
the X-ray crystal structures of 1 and 2, and an unprecedented observation
of extremely short relaxation times in a monohydride complex as well as in
the reaction of CpRuH(PPh3)(2) with a variety of acidic proton donors. The
relaxation is much faster than expected for a dipole-dipole process involvi
ng the two dihydrogen-bonded protons, but no origin for the effect could be
suggested. (C) Academie des sciences/Elsevier, Paris.