Preparation of dinuclear vinylidene complexes and their new deprotonation reactions

作者：Liu, Chung-Wei; Lin, Ying-Chih^*; Huang, Shou-Ling; Cheng, Cheng-Wei; Liu, Yi-Hung; Wang, Yu

来源：Organometallics, 2007, 26(14): 3431-3439.

DOI：10.1021/om060641o

• RUTHENIUM CYCLOPROPENYL COMPLEXES
• TRANSITION-METAL-COMPLEXES
• MIXED-VALENCE COMPLEXES
• SP CARBON CHAINS
• BRIDGING LIGAND
• ORGANOMETALLIC CHEMISTRY
• POLYYNEDIYL COMPLEXES
• ELECTRONIC-STRUCTURE
• COUPLING REACTIONS
• ALKYNYL COMPLEXES

The dinuclear dicationic vinylidene complex {[Ru]CC(Ph)CH2C(CH2CN)C[Ru]}(2+) (7a, [Ru] = Cp(PEt3)(2)Ru) is prepared from the reaction of ICH2CN with {[Ru]CC(Ph)CH2CC[Ru]}(+) (6a). Deprotonation of 7a by n-Bu4NOH is followed by a cyclization process yielding the stable complex 9a, containing a five-membered carbocyclic ring ligand, which is fully characterized by 2D-NMR analysis and a single-crystal X-ray diffraction analysis. Similarly deprotonation of {[Ru]CC(Ph)CH2C(CH2COOEt)C[Ru]}(2+) (8a) gave the stable product 11a containing a bridging ligand also with a similar five-membered carbocyclic ring. The cyclization process is affected by an ancillary ligand on the Ru metal center. Thus the analogous dinuclear complex 9b, with a bistriphenylphosphine ligand on one metal, which is prepared in a similar manner from {[Ru]CC(Ph)CH2C(CH2CN)C[Ru']}(2+) (7b, [Ru'] = Cp(PPh3)(2)Ru), is unstable, undergoing isomerization to give the dinuclear complex 10b, containing a cyclopropenyl ligand.

• 出版日期2007-7-2