Dissociation energies of O–H bonds in alkylseleno- and alkyltelluro-substituted phenols
- Autores: Denisova T.G.1, Denisov E.T.1
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Afiliações:
- Institute of Problems of Chemical Physics
- Edição: Volume 58, Nº 1 (2017)
- Páginas: 15-23
- Seção: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/162916
- DOI: https://doi.org/10.1134/S0023158417010013
- ID: 162916
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Resumo
The O−H bond dissociation energy (DO−H) has been determined for eight alkylseleno-substituted phenols, one alkyltelluro-substituted phenol, and one alkyltelluro-substituted pyridinol. DO−H has been estimated by the intersecting-parabolas method from kinetic data using five reference compounds: α-tocopherol (DO−H = 330.0 kJ/mol), 3,5-di-tert-butyl-4-methoxyphenol (DO−H = 347.6 kJ/mol), 4-methylphenol (DO−H = 361.6 kJ/mol), 2,6-di-tert-butyl-4-methylthiophenol (DO−H = 336.3 kJ/mol), and 2,6-di-ter-tbutyl-4-methylphenol (DO−H = 338.0 kJ/mol). The following DO−H values (kJ/mol) have been obtained: 335.9 for 2,5,7,8-tetramethyl-2-phytyl-6-hydroxy-3,4-dihydro-2H-1-benzoselenopyran, 342.6 for 2-methyl-5-hydroxy-2,3-dihydrobenzoselenophene, 333.5 for 2,4,6,7-tetramethyl-5-hydroxy-2,3-dihydrobenzoselenophene, 339.4 for 2-tert-butyl-4-methoxy-6-octylselenophenol, 357.9 for dodecyl 3-(4-hydroxyphenyl) propyl selenide, 348.5 for dodecyl 3-(3,5-dimethyl-4-hydroxyphenyl)propyl selenide, 350.9 for dodecyl 3-(3-tert-butyl-4-hydroxyphenyl)propyl selenide, 338.0 for dodecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl) propyl selenide, 343.0 for 2,6-di-tert-butyl-4-(tellurobutyl-4′-phenoxy)phenol, and 338.8 for 6-octyltelluro-3-pyridinol. The stabilization energies of phenoxyl radicals containing R substituents (X = O, S, Se, Te) have been compared.
Sobre autores
T. Denisova
Institute of Problems of Chemical Physics
Email: det@icp.ac.ru
Rússia, Chernogolovka, Moscow oblast, 142432
E. Denisov
Institute of Problems of Chemical Physics
Autor responsável pela correspondência
Email: det@icp.ac.ru
Rússia, Chernogolovka, Moscow oblast, 142432
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