Interconversions among the E⇆Z-Carotene Isomers: Theoretical Study
نویسندگان
1 Department of Chemistry, Faculty of Science, University of Sistan and Baluchestan, P. O. Box: 98135-674, Zahedan, Iran
2 Department of Chemistry, Faculty of Science, University of Sistan and Baluchestan, P .O. Box 98135-674, Zahedan, Iran
3 Department of Chemistry, Faculty of Science, University of Sistan and Baluchestan, P .O. Box 98135-674, Zahedan, Iran
doi
10.22036/pcr.2020.242676.1801چکیده
< p>The Minnesota functionalM062xwith 6-31+G(d, P) basis set has been employed to study interconversions among all-E-, 9Z-, 13Z- and 15Z-β-carotene isomers. Calculations provided essential data concerning the thermodynamic stabilities, the rate constants, activation energies, and HOMO and LUMO of all E⇆Z interconversions of β-carotene. The rate constants for the E⇆Z interconversions have been obtained with the transition-state theory based on the potential energy surface. In terms of energy, all-E-isomer was more stable than the Z-isomers, and the formation of the 9Z-isomer was the slowest interconversion, and raising the temperature increased the rate of interconversions. The tunnelling effect was negligible, and it was not taken into account in determining the rate constant of the E⇆Z interconversions.
