The thermal decomposition of 3,4-dihydro-2H-pyran (DHP, C ~H B O ) has been investigated by two methods: in shock waves with the laser-schlieren technique using mixtures of 5 and 10% DHP in krypton over 900-1500 K, 110-560 torr; in a flow tube having a reaction pressure 0.5 torr above atmospheric, u
Rate of the retro-Diels-Alder dissociation of 1,2,3,6-tetrahydropyridine over a wide temperature range
β Scribed by S. S. Sidhu; J. H. Kiefer; A. Lifshitz; C. Tamburu; J. A. Walker; W. Tsang
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 669 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Rate constants for the retro-Diels-Alder dissociation of 1,2,3,6-tetrahydropyridine, to 1,3-butadiene and methanimine, have been measured over 650-1450 K. To cover this range, three separate techniques were used at three laboratories: laser schlieren and single pulse shock tube methods, and a comparative rate flow system technique. The derived rate constants are extrapolated to the high-pressure limit with an RRKM model parameterized to fit the falloff observed in the laser-schlieren measurements. The resulting high-pressure rate con- stants show a reduction in activation energy of about 10 kcal/mol, comparing the isoelectronic cyclohexene, but little change in A-factor. There is an apparent increase in activation energy of 4 kcal/mol over the temperature range of these experiments, which is just outside probable error. Such a rise in activation energy is in marked contrast to the drop usually seen in simple bond fission, and may reflect a change from a concerted to a stepwise, biradical mechanism at high temperatures.
π SIMILAR VOLUMES
A flash photolysis system has been used to study the rate of reaction ( l ) , OH + CHI ---f The temperature It is found that the Arrhenius plot of kl is strongly CHI + H20, using time-resolved resonance absorption to monitor OH. was varied between 300 and 900Β°K. curved and k, ( T ) can best be rep