EARLY-LATE HETEROBIMETALLIC CHEMISTRY - REACTION OF A STABLE CARBENE ADDUCT OF [(C4ME4P)(2)YB](N) WITH RUTHENIUM HYDRIDES, TRANSIENT FORMATION OF A BIMETALLIC YB-RU HYDRIDE AND SYNTHESIS OF (C4ME4P)RUH(PPH3)(2)
P. Desmurs et al., EARLY-LATE HETEROBIMETALLIC CHEMISTRY - REACTION OF A STABLE CARBENE ADDUCT OF [(C4ME4P)(2)YB](N) WITH RUTHENIUM HYDRIDES, TRANSIENT FORMATION OF A BIMETALLIC YB-RU HYDRIDE AND SYNTHESIS OF (C4ME4P)RUH(PPH3)(2), Bulletin de la Societe chimique de France, 134(7), 1997, pp. 683-688
The new complexes (tmp)(2)Yb(carbene) 1a and 1b (tmp = C4Me4P and carb
ene = C2Me2((NPr)-Pr-i)(2)C and C2Me2(NMe2C)) have been synthesized fr
om [(tmp)(2)Yb](n) and characterized by elemental analysis and by NMR
(H-1, P-31). Complexes 1a and 1b are not stable in THF. Complex 1a rea
cts in benzene-d(6) with RuH4(PPh3)(3) to give the moderately stable h
eterobimetallic dihydride (PPh3)(2)RuH2-mu(tmp)(2)-Yb(carbene) 2a and
with RuHCl(PPh3)(3) to give (tmp)RuH(PPh3)(2) 4. The formation of the
analogous complex 2b is not observed when 1b is allowed to react with
RuH4(PPh3)(3). The nature of 2a is established by NMR. After two days
at room temperature, 2a is transformed into C2Me2((NPr)-Pr-i)(2)CH2 3a
, 4 and (tmp)RuH(PPh3) (carbene) 4'. Complex 4 was obtained analytical
ly pure from RuHCl(PPh3)(3) and tmpK whereas a mixture of 4 and 4' is
obtained after addition of an excess of C2Me2((NPr)-Pr-i)(2)CH2 to a s
olution of 4.