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Gas-phase kinetics and mechanism of diallyl sulfide thermal decomposition
Gholami, M. R ; Sharif University of Technology | 2003
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- Type of Document: Article
- DOI: 10.1002/poc.587
- Publisher: 2003
- Abstract:
- The gas-phase kinetics of diallyl sulfide pyrolysis were studied experimentally and theoretically in a static system over the temperature range 433-463 K and a total pressure of 80 Torr in a glass vessel with the free radical inhibitor cyclohexene. The experimental results show that this reaction is homogeneous, unimolecular and follows a first-order rate law. Theoretical studies at the B3LYP/6-31G* computational level indicate that the elimination reaction proceeds through a six-centered cyclic transition state and the reaction mechanism is concerted and non-synchronous. Copyright © 2003 John Wiley & Sons, Ltd
- Keywords:
- Concerted reaction ; Diallyl sulfide ; Homogeneity ; Non-synchronous ; Radical mechanism ; Thermal decomposition ; Unimolecular reaction
- Source: Journal of Physical Organic Chemistry ; Volume 16, Issue 3 , 2003 , Pages 153-157 ; 08943230 (ISSN)
- URL: https://onlinelibrary.wiley.com/doi/abs/10.1002/poc.587