Low-Temperature Photolysis of Benzoyl Peroxide
Autor: | A. I. Mikhailov, A. I. Bol’shakov, Alexander V. Kulikov, Svetlana I. Kuzina |
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Rok vydání: | 2020 |
Předmět: |
chemistry.chemical_classification
Double bond Radical Photodissociation Quantum yield 02 engineering and technology Benzoyl peroxide 010402 general chemistry 021001 nanoscience & nanotechnology Photochemistry 01 natural sciences Peroxide 0104 chemical sciences chemistry.chemical_compound Unpaired electron chemistry medicine Molecule Physical and Theoretical Chemistry 0210 nano-technology medicine.drug |
Zdroj: | Russian Journal of Physical Chemistry A. 94:189-195 |
ISSN: | 1531-863X 0036-0244 |
Popis: | The photolysis of dry benzoyl peroxide (BP) at 77 K in the 480–236 nm range of wavelengths and an ethanol solution is studied via EPR. It is determined that the main photochemical process in irradiating BP at λ = 480–365 nm is the direct photodissociation of the O–O peroxide bonds and C–H bonds of benzene rings to form benzoyloxy radicals and atomic hydrogen, which likely forms via a two-quantum mechanism. The quantum yield of primary intermediates is φ ≈ 2.7 × 10−5. Upon subsequent irradiation of a sample using light with λ = 300–236 nm, benzoyloxy radicals release carbon dioxide and transform into phenyl radicals with a quantum yield of φ ≈ 3 × 10−4. At 120–145 K, phenyl radicals react with double bonds of aromatic rings of PB to form phenyl-substituted cyclohexadienyl radicals vanishing at 273 K. Quantum chemical calculations of the radical structures of photolyzed peroxide are made with the density functional approach (B3LYP/6-311g), and good agreement between the experimental and theoretical parameters is noted. Calculations show that in the structure of benzoyloxy radicals, the spin density is distributed almost equally between the two oxygen atoms of the radical, due to the conjugation of the unpaired electron to the lone p electron pair on the oxygen atom of the C=O group. In the photolysis of BP solutions in ethanol at λ ≥ 365 nm, solvent radicals form via sensitized photolysis through the reaction between primary benzoyloxy radicals and solvent molecules. |
Databáze: | OpenAIRE |
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