SYNTHESIS AND REACTIVITY OF TRIRUTHENIUM CARBONYL CLUSTER COMPLEXES CONTAINING A BRIDGING 1-AZAVINYLIDENE LIGAND DERIVED FROM BENZOPHENONE IMINE

Citation
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
Citations number
51
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
15
Issue
13
Year of publication
1996
Pages
3004 - 3010
Database
ISI
SICI code
0276-7333(1996)15:13<3004:SAROTC>2.0.ZU;2-L
Abstract
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.