CONFIGURATIONAL ISOMERIZATION OF CIS-1,2-DIMETHYLCYCLOHEXANES, CIS-1,3-DIMETHYLCYCLOHEXANES AND CIS-1,4-DIMETHYLCYCLOHEXANE AND TRANS-1,2-DIMETHYLCYCLOHEXANES, TRANS-1,3-DIMETHYLCYCLOHEXANES AND TRANS-1,4-DIMETHYLCYCLOHEXANES
F. Notheisz et al., CONFIGURATIONAL ISOMERIZATION OF CIS-1,2-DIMETHYLCYCLOHEXANES, CIS-1,3-DIMETHYLCYCLOHEXANES AND CIS-1,4-DIMETHYLCYCLOHEXANE AND TRANS-1,2-DIMETHYLCYCLOHEXANES, TRANS-1,3-DIMETHYLCYCLOHEXANES AND TRANS-1,4-DIMETHYLCYCLOHEXANES, Journal of the Chemical Society. Faraday transactions, 93(21), 1997, pp. 3807-3811
Citations number
32
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
Configurational isomerization (henceforth isomerization) of cis-and tr
ans-1,2-, 1,3-, and 1,4-dimethylcyclohexanes (henceforth c-1,2, 1,3, 1
,4 and t-1,2, 1,3, 1,4) has been studied under identical experimental
conditions on supported Pt catalyst in the temperature range 373-548 K
and partial pressure of hydrogen range 13.3-100 kPa. The effect of te
mperature and hydrogen pressure on the reaction rates as well as the a
ctivation energies were determined. Plotting the rates of isomerizatio
n against temperature reveals maxima. The rate of isomerization of t-1
,3, increases with increasing hydrogen pressure. Isomers containing ax
ial-equatorial (henceforth a,e) methyl groups were converted at a high
er rate than those containig diequatorial methyl groups (henceforth e,
e). At lower temperatures the experimental data maybe interpreted by t
he 'roll-over' mechanism, while at higher temperatures the pi-allyl me
chanism proceeding via more unsaturated surface intermediates is invok
ed.