Quantum-chemical study of energies of maleimide and itaconimide isomeric derivatives

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

For 38 pairs of the isomeric derivatives of maleimide and itaconimide, the Gibbs free energies were calculated using the density functional theory (DFT) and domain-based local pair natural orbital (DLPNO) methods. The effects of the solvent and of substituents in positions 1, 3, and 4 of the maleimide ring on the energy difference of the isomers were studied. Depending on the substituents and conditions, the equilibrium can shift toward the maleimide or itaconimide form. Further migration of the double bond and cis-trans- isomerism were also considered wherever possible.

Толық мәтін

Рұқсат жабық

Авторлар туралы

A. Panov

Gause Institute of New Antibiotics

Хат алмасуға жауапты Автор.
Email: 7745243@mail.ru
Ресей, Moscow, 119021

Әдебиет тізімі

  1. Ravasco J.M.J.M., Faustino H., Trindade A., Gois P.M.P. // Chem. Eur. J. 2019. V. 25. P. 43.
  2. Elschner T., Obst F., Heinze T. // Macromol. Biosci. 2018. V. 18. P. 1800258.
  3. Wei K., Wen G., Zhao Y. et al. // J. Mater. Chem. C. 2016. V. 41(4). P. 9804.
  4. Oz Y., Sanyal A. // Chem. Rec. 2018. V. 18. P. 570.
  5. Aqueveque P., Anke T., Sterner O. // Zeitschrift für Naturforschung C. 2002. V. 57(3—4). P. 257.
  6. Yuan C., Yang H., Gong Q., et al. // Adv. Synth. Catal. 2021. V. 363. P. 3336.
  7. Askri S., Edziri H., Hamouda M.B. et al. // J. Molec. Struc. 2022. V. 1250. P. 131688.
  8. Albakhit S.D.Y., Mutlaq D.Z., Al-Shawi A.A.A. // Chem. Africa. 2023. V. 6. P. 2933.
  9. Gherbovet O., Garcia Alvarez M.C., Bignon J., Roussi F. // J. Med. Chem. 2016. V. 59(23). P. 10774.
  10. Galanti M.C., Galanti A.V. // J. Org. Chem. 1982. V. 47(8). P. 1572.
  11. Paramonova P., Sharonova T., Kalinin S., et al. // Mendeleev Commun. 2022. V. 32(2). P. 176.
  12. Haval K.P., Argade N.P. // J. Org. Chem. 2008. V. 73. P. 6936.
  13. Inyutina A., Kantin G., Dar′in D., Krasavin M. // J. Org. Chem. 2021. V. 86. P. 13673.
  14. Laha D., Meher K.B., Bankar O.S., et al. // Asian J. Org. Chem. 2022. V. 11, e202200062.
  15. Neese F. // Wiley Interdiscip. Rev. Comput. Mol. Sci. 2012. V. 2. P. 73.
  16. Weigend F., Ahlrichs, R. // Phys. Chem. Chem. Phys. 2005. V. 7. P. 3297.
  17. Weigend F. // Phys. Chem. Chem. Phys. 2006. V. 8. P. 1057.
  18. Barone V., Cossi M. // J. Phys. Chem. A. 1998. V. 102(11). P. 1995.
  19. Riplinger C., Sandhoefer B., Hansen A., Neese F. // J. Chem. Phys. 2013. V. 139. P. 134101.
  20. Huang X., Sha F. // J. Org. Chem. 2008. V. 73. P. 1173.
  21. Chupakhin E., Gecht M., Ivanov A. et al. // Synthesis. 2021. V. 53(07). P. 1292.
  22. Панов А.А. // Докл.РАН. Химия, науки о материалах. 2023. Т. 508(1). С. 111. [Panov A.A. // Doklady Phys. Chem. 2023. V. 508(2). P. 28.]
  23. Chupakhin E., Kantin G., Dar’in D., Krasavin M. // Mendeleev Commun. 2022. V. 32. P. 382.
  24. Inyutina A., Dar’in D., Kantina G., Krasavin M. // Org. Biomol. Chem. 2021. V. 19. P. 5068.

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
2. Fig. 1. Structure of hymanimides 1a, b and biologically active arylidenesuccinimides 2 and (indol-3-yl)methylmaleimide 3.

Жүктеу (127KB)
3. Fig. 2. Isomerization of itaconic anhydride 4 to citraconic anhydride 5 and migration of the double bond in (arylidene)succinimides 6a, 7a.

Жүктеу (144KB)
4. Fig. 3. Structures of isomeric derivatives of maleimide (a) and itaconimide (b).

Жүктеу (52KB)
5. Fig. 4. General structures of isomeric itaconimides 8–35 (a) and maleimides (b).

Жүктеу (50KB)
6. Fig. 5. Cis-trans isomerism using the example of 3-benzylidene-4-methylsuccinimide (8a).

Жүктеу (44KB)
7. Fig. 6. Isomeric N-substituted maleimides and itaconimides 8, 36–38, as well as anhydrides 39 and anions 40.

Жүктеу (61KB)
8. Fig. 7. Isomers of 3-benzyl-4-(3-methylbut-2-en-1-yl)maleimide 41b.

Жүктеу (60KB)
9. Fig. 8. Isomeric annelated maleimides and itaconimides.

Жүктеу (97KB)

© Russian Academy of Sciences, 2025