Solvent and substituent effects on the kinetics of thermolysis of cis-fused 1,2,4-trioxanes
The kinetics of the thermal decomposition reaction of <i>cis</i>-6-phenyl-5,6-(2- phenylpropyliden)-3,3-pentamethylene-1,2,4-trioxacyclohexane <b>(Ia)</b> were investigated in benzene and methanol solutions in the temperature and concentration ranges of 353.3-413.2 K and (1.1...
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| Autores principales: | , |
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| Formato: | Articulo |
| Lenguaje: | Inglés |
| Publicado: |
2001
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| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/35056 http://www.mdpi.com/1420-3049/6/8/699 |
| Aporte de: |
| Sumario: | The kinetics of the thermal decomposition reaction of <i>cis</i>-6-phenyl-5,6-(2- phenylpropyliden)-3,3-pentamethylene-1,2,4-trioxacyclohexane <b>(Ia)</b> were investigated in benzene and methanol solutions in the temperature and concentration ranges of 353.3-413.2 K and (1.1 - 13.1)×10<SUP>-3</SUP> M, respectively. First-order rate constant values were obtained for up to at least ca. 20% conversions of that cyclic peroxide. The activation parameter values for the initial unimolecular homolysis of that molecule, results supported by the effect of the addition of di-<i>tert</i>-butyl-<i>p</i>-cresol as a free radical scavenger, indicate a stepwise reaction mechanism which is in keeping with the reaction products analysis. The corresponding activation parameters for the reaction of <b>Ia</b> in methanol (ΔH<SUP>#</SUP> = 20.2 ± 0.6 kcal mol<SUP>-1</SUP>; ΔS<SUP>#</SUP> = 0.1 ± 1.6 cal mol<SUP>-1</SUP>K<SUP>-1</SUP>; ΔG<SUP>#</SUP> = 20.2 ± 0.6 kcal mol<SUP>-1</SUP> and in benzene (ΔH<SUP>#</SUP> = 15.4 ± 0.2 kcal mol<SUP>-1</SUP>; ΔS<SUP>#</SUP> = -13.2 ± 0.5 cal mol<SUP>-1</SUP>K<SUP>-1</SUP>; ΔG# = 20.5 ± 0.2 kcal mol<SUP>-1</SUP> solutions are compared with values obtained for cis-6-phenyl-5,6-(2-phenylpropyliden)-3,3- tetramethylene-1,2,4-trioxacyclohexane (<b>Ib</b>) thermolysis in the same solvents. The thermolysis kinetics of <b>Ia</b> are less sensitive to solvent changes compared to the behaviour already reported for the analogous reactions of <b>Ib</b>. Because both molecules in solution are flexible structures due to their configurations, the relatively small solvent effect found on the former trioxane reaction is attributed to the extent of the chain of methylene groups attached on C-3 of the corresponding molecular rings. Furthermore, the pertinent substituent effect on the peroxidic bond strength of those molecules in solution was evaluated. |
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