Cross-coupling organometallic catalysis

Herrmann, W. A. The Suzuki cross-coupling. App//ed Homogeneous Catalysis with Organometallic Compounds (2nd Edition) 2002,1, 591-598. 

Here triphenylphosphine, the most important ligand in organometallic catalysis, is coupled to the benzene rings of cross-linked polystyrene. An anchored catalyst is then formed by coordination of the phosphine group to the metal center of a rhodium complex (Eq. 6-2). 

Phosphinocarbene or 2 -phosphaacetylene 4, which is in resonance with an ylide form and with a form containing phosphoms carbon triple bond, is a distillable red oil. Electronic and more importantly steric effects make these two compounds so stable. Carbene 4 adds to various electron-deficient olefins such as styrene and substituted styrenes. Bertrand et al. have made excellent use of the push-pull motif to produce the isolable carbenes 5 and 6, which are stable at low temperature in solutions of electron-donor solvents (THF (tetrahydrofuran), diethyl ether, toluene) but dimerizes in pentane solution. Some persistent carbenes are used as ancillary ligands in organometallic chemistry and in catalysis, for example, the ruthenium-based Grubbs catalyst and palladium-based catalysts for cross-coupling reactions. 

An Organometallic Com pound That Occurs Naturally Coenzyme B,2 591 Organocopper Reagents 592 Palladium-Catalyzed Cross-Coupling 595 Homogeneous Catalytic Hydrogenation 597 Olefin Metathesis 600 Ziegler-Natta Catalysis of Alkene Polymerization 603 Summary 606 Problems 608... 

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