Selective Catalytic Hydrodimerization of 1,3-Butadiene by Palladium Compounds Dissolved in Ionic Liquids
journal contributionposted on 31.01.1998 by Jeane E. L. Dullius, Paulo A. Z. Suarez, Sandra Einloft, Roberto F. de Souza, Jairton Dupont, Jean Fischer, André De Cian
Any type of content formally published in an academic journal, usually following a peer-review process.
Palladium(II) compounds dissolved in 1-n-butyl-3-methylimidazolium tetrafluoroborate (BMI·BF4) ionic liquid are shown to be able to catalyze the hydrodimerization of 1,3-butadiene. In most of the cases, only the 1,3-butadiene dimer 1,3,6-octatriene and the telomer octa-2,7-dien-1-ol have been obtained. The products' selectivity and catalytic activity depend on the reaction conditions. 1,3-Butadiene conversion up to 28%, a turnover frequency (TOF) of 118 h-1, and a selectivity of 94% on telomer were achieved with (BMI)2PdCl4 dissolved in BMI·BF4. The 1,3-butadiene conversion and TOF were significantly increased to 49% and 204 h-1, respectively, by a 5-atm pressure of carbon dioxide. The reactions were performed under homogeneous conditions at 70 °C. However, at temperatures below 5 °C, a two-phase system is formed and the products are easily removed from the reaction mixture by simple decanting. The recovered ionic catalyst solution can be reused several times without any significant changes in the catalytic performance. The structure of the new catalyst precursor (BMI)2PdCl4 has been determined by X-ray diffraction analysis.