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   <subfield code="a">Competitive hydrogenation in binary diene systems on a palladium catalyst</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Jiri Krupka, Zdenek Severa, Josef Pasek]</subfield>
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   <subfield code="a">Summary: Hydrogenations of individual C5 dienic substrates (1,3-cyclopentadiene, isoprene, 1,4-pentadiene, cis-1,3-pentadiene, trans-1,3-pentadiene) and their binary mixtures on a heterogeneous palladium catalyst were studied in cyclohexane at 25°C and 2 MPa. Selectivities of the competitive hydrogenations were determined and the substrates relative adsorption coefficients calculated. Effects of the diene structure on their reactivity and the stability of the surface complex are discussed. It was found that differences in selectivity of the competitive hydrogenations of C5 dienes are caused by the difference both in adsorptivity values and in reactivity of adsorbed molecules. The presence of a five-membered ring in the C5 dienes leads, , in significant reduction of surface complex stability as compared with acyclic structures of C5 dienes. On the other hand, it has a very positive effect on the rate of surface reaction.</subfield>
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   <subfield code="a">cis-1</subfield>
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   <subfield code="u">Department of Organic Technology, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic</subfield>
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   <subfield code="t">Reaction Kinetics and Catalysis Letters</subfield>
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