Mechanism of the Photochemical Isomerization and Oxidation of 2-Butenedial: A Theoretical Study

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 13; p. 4994
• Main Authors: Maranzana, Andrea, Tonachini, Glauco
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26-06-2023; MDPI
• Subjects: 2-butenedial; CASSCF; CCSD(T); Computer software industry; DFT; Energy; Excitation; Furans; Furans - chemistry; Ground state; Hydrogen; Hyperspaces; Investigations; Irradiation; Isomerism; Isomerization; Maleic anhydride; Maleic Anhydrides - chemistry; Models, Theoretical; Oxidants; Oxidation; Oxidizing agents; Photochemicals; Photochemistry; Radiation; reaction mechanism; Reaction mechanisms; Singlet oxygen; Solar radiation; Troposphere; tropospheric oxidation; Water - chemistry; United States; DFT; CCSD(T); reaction mechanism; 2-butenedial; tropospheric oxidation; CASSCF
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28134994

Under tropospheric conditions, 2-butenedial is photochemically removed to produce secondary organic aerosol. Upon solar irradiation in the lower troposphere, the main photochemical products are ketene-enol (a key intermediate product), furanones, and maleic anhydride. The oxidative reaction mechanism was studied using the multireference method CASSCF to explore the hypersurface of the two most accessible singlet excited states, and by DFT for the ground state. Photoisomerization of 2-butenedial in the first excited state directly produces ground state ketene-enol upon nonradiative relaxation. From this intermediate, furan-2-ol and successively 3H-furan-2-one and 5H-furan-2-one are formed. The cooperative effect of two water molecules is essential to catalyze the cyclization of ketene-enol to furan-2-ol, followed by hydrogen transfers to furanones. Two water molecules are also necessary to form maleic anhydride from furan-2-ol. For this last reaction, in which one extra oxygen must be acquired, we hypothesize a mechanism with singlet oxygen as the oxidant.