Enviar artigo por via de e-mail DFT STUDY OF KETO-ENOL EQUILIBRIUM AND GLOBAL ELECTROPHILICITY OF HYDROXYMALEIMIDE DERIVATIVES
- Autores: Panov A.1
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Afiliações:
- Gause Institute of New Antibiotics
- Edição: Volume 508, Nº 1 (2023)
- Páginas: 111-116
- Seção: ФИЗИЧЕСКАЯ ХИМИЯ
- URL: https://journals.rcsi.science/2686-9535/article/view/135972
- DOI: https://doi.org/10.31857/S2686953522600325
- EDN: https://elibrary.ru/EVQYQM
- ID: 135972
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Resumo
For 36 3-hydroxymaleimide derivatives energies of enol and keto forms were calculated by DFT method. The results clearly show that with only few exceptions, enol form is energetically more favourable by 16–60 kJ mol–1, with energy difference depending on 4-substituent. Global electrophilic index was calculated for all the compounds in question, showing that keto form is generally more electrophilic, with electrophilicity strongly dependending on 4-substituent. Two possible structures of hydroxymaleimide anion were evaluated, with deprotonated oxygen atom being the most energetically favourable.
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Sobre autores
Alexey Panov
Gause Institute of New Antibiotics
Autor responsável pela correspondência
Email: 7745243@mail.ru
Russian, 119021, Moscow
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