Atmospheric chemistry of oxazole: The mechanism and kinetic studies of the oxidation reaction initiated by OH radicals

Abolfazl Shiroudi, Mohamed A. Abdel-Rahman, Ahmed M. El-Nahas, Mohammednoor Altarawneh

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

The oxidation reaction of oxazole initiated by OH radicals is studiedviaOH-addition and H-abstraction reactions using DFT (M06-2X and ωB97XD methods) under atmospheric conditions coupled with reaction kinetics calculations using transition state (TST) and Rice-Ramsperger-Kassel-Marcus (RRKM) theories. The obtained results show that OH˙ radical attack onto different carbons (OH-addition) proceeds faster than OH˙ attack onto H atoms bonded to the different carbons (H-abstraction) by several orders of magnitude. Furthermore, the pressure and temperature effects on the kinetic rates have been considered using RRKM calculations. Effective kinetic rate coefficients (keff) demonstrate that the two-step reaction mechanism prevails. Based on the experiment, it can be concluded that the most favorable process related to hydroxyl attack onto the carbon which is adjacent to the oxygen has a lower barrier height from a kinetic viewpoint. Branching ratios (BRs) also demonstrate that the regioselectivity decreases with decreasing pressure and increasing temperature. Despite the negative energy barriers,P> 100 bar is required in order to reach the high-pressure (H-P) limit.

Original languageEnglish
Pages (from-to)2237-2248
Number of pages12
JournalNew Journal of Chemistry
Volume45
Issue number4
DOIs
Publication statusPublished - Jan 28 2021

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Atmospheric chemistry of oxazole: The mechanism and kinetic studies of the oxidation reaction initiated by OH radicals'. Together they form a unique fingerprint.

Cite this