C-C BEND FORMATION BETWEEN VINYLIDENE AND ALKYNYL LIGANDS AT RUTHENIUM(II) LEADING TO EITHER ENYNYL OR DIENYNYL COMPLEXES

Citation
C. Bianchini et al., C-C BEND FORMATION BETWEEN VINYLIDENE AND ALKYNYL LIGANDS AT RUTHENIUM(II) LEADING TO EITHER ENYNYL OR DIENYNYL COMPLEXES, Organometallics, 15(1), 1996, pp. 272-285
Citations number
105
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
15
Issue
1
Year of publication
1996
Pages
272 - 285
Database
ISI
SICI code
0276-7333(1996)15:1<272:CBFBVA>2.0.ZU;2-E
Abstract
The Ru(II) complex mer,trans-(PNP)RuCl2(PPh(3)) (1) reacts with either phenylacetylene or p-tolylacetylene to give fac,cis-(PNP)RuCl2(C=CH(R )} (R = Ph (2), p-tolyl (3)) in refluxing tetrahydrofuran (THF) and me r,trans-(PNP)RuCl2{C=CH(R)} (R = Ph (4), p-tolyl (5)) in a refluxing T HF/EtOH mixture (1:2 v:v) [PNP = CH3CH2CH2N(CH(2)CH(2)PPh(2))(2)]. The fac,cis vinylidene complexes 2 and 3 react with an excess of LiC=CPh converting to the sigma-alkynyl-eta(3)-enynyl complexes anti,mer-(PNP) Ru(C=CPh){eta(3)-PhC(3)=CH(Ph)} (8) and nti,mer-(PNP)-Ru(C=CPh){eta(3) -PhC(3)=CH(p-tolyl)} (9), respectively. Conversely, treatment of the m er,trans vinylidene isomers with an excess of LiC=CPh, followed by add ition of a primary alcohol, exclusively gives the sigma-alkynyl-eta-di enynyl complexes mer-(PNP)Ru(C=CPh){eta-PhC=C-(C=CPh)CH=CH(R)} (R Ph, 12; R = p-tolyl, 13). Single-crystal X-ray analyses have been carried out on 8 and 13. In both compounds the coordination geometry around th e Ru atom approximates an octahedron with three positions taken by a m er PNP ligand and one position taken by a phenylethynyl group. The coo rdination sphere around the metal center is completed by an eta(3)-1,4 -diphenylbut-3-en-1-ynyl ligand in 8 and by a 3-(phenylethynyl)-4-phen ylbuta-1(E),3(Z)-dien-4-yl ligand in 13. The latter ligand essentially uses the C-1 carbon atom to bind the metal, although a weak bonding i nteraction may be envisaged also with the alkynyl substituent in the 3 -position. A single-crystal X-ray analysis has also been carried out o n the octahedral fac,cis-(PNP)RuCl2(CO) complex obtained by treatment of the vinylidenes 2 and 3 with molecular oxygen. The influence of the bonding mode of the PNP ligand on the different reactivity shown by t he fac and mer vinylidene complexes toward LiC=CPh is discussed in lig ht of a multiform experimental study (X-ray structure determinations, multinuclear NMR spectroscopy, deuterium- and p-tolyl-labeling experim ents, independent reactions with isolated compounds).