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Radiolytic redistribution of H and O atoms in acetylacetone
Institution:1. Department of Chemistry and Technology, Tver State University, 170100 Tver, Russian Federation;2. All-Russian Scientific Research Institute for Physical-Engineering and Radiotechnical Metrology, 141570 Mendeleevo, Moscow Region, Russian Federation;3. V. N. Orekhovich Institute of Biomedical Chemistry, 119121 Moscow, Russian Federation;1. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119334 Moscow, Russian Federation;2. D. I. Mendeleev University of Chemical Technology of Russia, 125047 Moscow, Russian Federation;3. M. M. Shemyakin–Yu. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russian Federation;4. Department of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russian Federation;1. Institute of Macromolecular Compounds, Russian Academy of Sciences, 199004 St. Petersburg, Russian Federation;2. Saint-Petersburg State University of Industrial Technologies and Design, 191186 St. Petersburg, Russian Federation;3. St. Petersburg State Institute of Technology (Technical University), 190013 St. Petersburg, Russian Federation;4. Institute of Earth Sciences, St. Petersburg State University, 199034 St. Petersburg, Russian Federation
Abstract:Compared to ambient conditions, radiolysis of boiling acetylacetone almost halved the yield of C–OH bond cleavage and doubled the redistribution of H atoms
Keywords:acetylacetone  4-hydroxypent-3-en-2-one  pentane-2  4-dione  radiolysis  boiling  radical cation  proton transfer  isomers
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