Peculiarities in the Radiolysis of β-Diketones

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Resumo

Intramolecular hydrogen bonding has a significant effect on the radiolytic transformations of β- diketones. Using the radiolysis of acetylacetone as an example, it has been shown that a hydrogen bond between the hydroxyl and carbonyl in an enol prevents proton transfer from the primary radical cation to the neighboring molecule. As a result, the radiolytic formation of a keto alcohol (4-hydroxy-2-pentanone) was not observed at room temperature, but it was effective under boiling conditions. The intramolecular hydrogen
bond contributed to a significant structural stress in the radical cation, which increased the yield of C–OH bond cleavage and the inhomogeneous formation of acetate (4-oxopent-2-en-2-yl acetate) under normal conditions

Sobre autores

S. Vlasov

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: ponomarev@ipc.rssi.ru
Moscow, 119071 Russia

A. Smirnova

Faculty of Chemistry, Moscow State University

Email: ponomarev@ipc.rssi.ru
Moscow, 119991 Russia

A. Ponomarev

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: ponomarev@ipc.rssi.ru
Moscow, 119071 Russia

D. Uchkina

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: ponomarev@ipc.rssi.ru
Moscow, 119071 Russia

A. Sholokhova

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: ponomarev@ipc.rssi.ru
Moscow, 119071 Russia

A. Mitrofanov

Faculty of Chemistry, Moscow State University

Autor responsável pela correspondência
Email: ponomarev@ipc.rssi.ru
Moscow, 119991 Russia

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Declaração de direitos autorais © С.И. Власов, А.А. Смирнова, А.В. Пономарев, Д.А. Учкина, А.Ю. Шолохова, А.А. Митрофанов, 2023

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