Abstract
Addition of CO to [1,2,4-(Me3C)3C5H2]2CeH, Cp¢2CeH, in toluene yields the cis- (Cp¢2Ce)2(í-OCHCHO), in which the cis-enediolate group bridges the two metallocene fragments. The cisenediolate quantitatively isomerizes intramolecularly to the trans-enediolate in C6D6 at 100 °C over 7 months. When the solvent is pentane, Cp¢2Ce(OCH2)CeCp¢2 forms, in which the oxomethylene group or the formaldehyde dianion bridges the two metallocene fragments. The cis-enediolate is suggested to form by insertion of CO into the Ce-C bond of Cp¢2Ce(OCH2)CeCp¢2, generating Cp¢2CeOCH2COCeCp¢2. The stereochemistry of the cis-enediolate is determined by a 1,2-hydrogen shift in the OCH2CO fragment that has the OC(H2) bond anti-periplanar relative to the carbene lone pair. The bridging oxomethylene complex reacts with H2, but not with CH4, to give Cp¢2CeOMe, which is also the product of the reaction between Cp¢2CeH and a mixture of CO and H2. The oxomethylene complex reacts with CO to give the cis-enediolate complex. DFT calculations on C5H5 model metallocenes show that the reaction of Cp2CeH with CO and H2 to give Cp2CeOMe is exoergic by 50 kcal mol-1. The net reaction proceeds by a series of elementary reactions that occur after the formyl complex, Cp2Ce(è2-CHO), is formed by further reaction with H2. The key point that emerges from the calculated potential energy surface is the bifunctional nature of the metal formyl in which the carbon atom behaves as a donor and acceptor. Replacing H2 by CH4 increases the activation energy by 17 kcal mol-1.