Pl. Andreu et al., SYNTHESIS AND REACTIVITY OF TRIRUTHENIUM CARBONYL CLUSTER COMPLEXES CONTAINING A BRIDGING 1-AZAVINYLIDENE LIGAND DERIVED FROM BENZOPHENONE IMINE, Organometallics, 15(13), 1996, pp. 3004-3010
The reaction of [Ru-3(CO)(12)] with the lithium salt of benzophenone i
mine (LiN=CPh(2)) followed by protonation with trifluoroacetic acid le
ads to the eta(1)-1-azavinylidene cluster complex [Ru-3(mu-H)(mu-N=CPh
(2))(CO)(10)] (1). Compound 1 cannot be prepared by direct reaction of
[Ru-3(CO)(12)] with benzophenone imine under thermal conditions. Carb
onyl substitution and thermolysis reactions on compound 1 and on some
of its derivatives are described. Complex 1 reacts with 1 and 2 equiv
of bis(diphenylphosphino)methane (dppm) at room temperature to give th
e substituted derivatives [Ru-3(mu-H)(mu-N=CPh(2))(mu-dppm)(CO)(8)] (2
) and [Ru-3(mu-H)(mu-N=CPh(2))(mu-dppm)(dppm)(CO)(7)] (3), respectivel
y. In both complexes the three bridging Ligands span the same Ru-Ru ed
ge; in addition, complex 3 contains an yl-dppm ligand occupying an equ
atorial site on the unique Ru atom. An X-ray structure analysis of 3 .
0.5CH(2)Cl(2) is reported. Thermolysis of complex 2 in THF at reflux
temperature leads to [Ru-3(mu-H)(mu(3)-N=CPh(2))(mu-dppm)(CO)(7)] (4),
a compound which contains a bridging eta(2)-1-azavinylidene ligand in
teracting with the three Ru atoms. Complex 4 reacts with CO (1 atm, 18
degrees C) reverting to complex 2. The reaction of compound 1 with PP
h(3) at room temperature gives the monosubstituted derivative [Ru-3(mu
-H)(mu-N=CPh(2))(PPh(3))(CO)(9)] (5), in which the P-donor ligand is a
ttached to one of the two bridged Ru atoms. Thermolysis of 5 in THF at
reflux temperature leads to [Ru-3(mu-H)(mu(3)-N=CPh(2))(PPh(3))(CO)(8
)] (6), which, as complex 4, contains a face-bridging eta(2)-1-azaviny
lidene ligand. The reaction of complex 5 with PPh(3) occurs only at hi
gher temperatures (40-70 degrees C) to give the asymmetrically disubst
ituted derivative [Ru-3(mu-H)(mu-N=CPh(2))(PPh(3))(2)(CO)(8)] (7), whi
ch has the additional PPh(3) ligand attached to the unbridged Ru atom.
Compound 7 is thermally unstable, undergoing an easy (40-70 degrees C
) orthometalation reaction of a phenyl ring of the azavinylidene ligan
d to give the derivative Ru-3(mu-H)(2)(mu-N=CPhC(6)H(4))(PPh(3))(2)(CO
)(7)] (8). This compound reacts with CO (1 atm, 18 degrees C) to regen
erate complex 7.