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Structure and Bonding in Metal Alkene Complexes

Probably the first metal alkene complex was Zeise s salt, K[Pt(C2H4)Cl3] or the bridged compound [PtCl2(C2H4)]2. These compounds were first prepared by Zeise in about 1825. The palladium analogs of these compounds are also now known. A large number of metal alkene complexes are known, and some of the chemistry of these materials will be described here. [Pg.754]

In this case, the bond between the carbon atoms is about the same as it is for a C-C single bond. Moreover, unlike the anion of Zeise s salt, the carbon atoms are in the plane formed by platinum and the other ligands. Clearly, this represents a significant difference from the usual alkene complexes. In essence, a three-membered C-P-C ring is formed. It appears in this case that the ability of the [Pg.755]

CHAPTER 21 Complexes Containing Metal-Carbon and Metal-Metal Bonds [Pg.756]

Other organic ligands can be bound in more than one way also. For example, the allyl group can be bound by a cr-bond between the metal and one carbon atom (rf) or as a 7r donor encompassing all three carbon atoms (ry3)  [Pg.757]

Butadiene can function as a donor of four electrons in which the bonding is delocalized. A complex of this type is Fe(CO)3(774-C4H8)( which has the structure [Pg.758]


See other pages where Structure and Bonding in Metal Alkene Complexes is mentioned: [Pg.754]    [Pg.755]    [Pg.757]    [Pg.759]   


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