Carbon-carbon coupling reactions on triruthenium clusters: synthesis and structure of Ru-3(CO)(9)[mu(3)-eta(3)-PhCCCC(H)Ph][mu(2)-NS(O)MePh] and Ru-3(mu(2)-CO)(CO)(7)[mu(3)-eta(3)-PhCCCC(H)Ph][mu(3)-NS(O)MePh]
Author(s)
Ferrand, Vincent
Gambs, Céline
Derrien, Nadine
Bolm, Carsten
Date issued
1997
In
Journal of Organometallic Chemistry
Vol
1-2
No
549
From page
275
To page
282
Subjects
clusters ruthenium alkynes carbon-carbon coupling crystal structures ALPHA-DIIMINE COMPLEXES INTRAMOLECULAR TRANSANNULAR CYCLIZATIONS TRANSITION-METAL COMPOUNDS BOND-FORMING REACTIONS X-RAY STRUCTURES CRYSTAL-STRUCTURE MOLECULAR-STRUCTURE RUTHENIUM CLUSTERS CHEMICAL-TRANSFORMATIONS MACROCYCLIC ALKADIYNES
Abstract
The reaction of the electron-deficient cluster (mu(2)-H)Ru-3(CO)(9)[mu(3)-NS(O)MePh] (1) with para-nitrotolane gives, with coupling of two alkyne units and elimination of the para-nitrophenyl fragment, the trinuclear complexes Ru-3(CO)(9)[mu(3)-eta(3)-PhCCCC(H)Ph][mu(2)-NS(O)MePh] (2) and Ru-3(mu(2)-CO)(CO)(7)[mu(3)-eta(3)-PhCCCC(H)Ph][mu(3)-NS(O)MePh] (3). The resulting organic moiety, coordinated as mu(3)-eta(3)-5e-donor, is best considered as a butenynyl (PhC=C-C=C(H)Ph) ligand in 2 and as a butatrienyl (PhC=C=C=C(H)Ph) ligand in 3. From the reaction mixture, the two isomeric vinyl complexes Ru-3(mu(2)-CO)(2)(CO)(6)[mu(2)-eta(2)-PhC=C(H)(C6H4-p-NO2)][mu(3)-NS(O)M ePh] (4a) and Ru-3(mu(2)-CO)(2)(CO)(6)[mu(2)-eta(2)-(C6H4-P-NO2)-C=C(H)Ph]-[mu(3)-NS(O )MePh] (4b) complexes can also be isolated. (C) 1997 Elsevier Science S.A.
Publication type
journal article