Quantum-Chemical Study of Catalysis in the Reaction of N,O-Dimethyl Carbamate with Methylamine
- Авторлар: Samuilov A.Y.1, Kozhanova E.P.1, Samuilov Y.D.1
- 
							Мекемелер: 
							- Kazan National Research Technological University
 
- Шығарылым: Том 95, № 1-2 (2025)
- Беттер: 17-26
- Бөлім: Articles
- URL: https://rjeid.com/0044-460X/article/view/679800
- DOI: https://doi.org/10.31857/S0044460X25010036
- EDN: https://elibrary.ru/AHPUPQ
- ID: 679800
Дәйексөз келтіру
Аннотация
Non-catalytic and sodium acetate and sodium methoxide catalyzed reactions of N,O-dimethyl carbamate with methylamine were studied using quantum-chemical hybrid density functional methods M06 and B3LYP. All interactions proceed through concerted cyclic transition states. Non-catalytic and sodium acetate-catalyzed reactions are characterized by a large activation free energy barrier. The transformation catalyzed by sodium methoxide is characterized by a negative enthalpy of activation and a low free energy of activation.
Негізгі сөздер
Толық мәтін
Авторлар туралы
A. Samuilov
Kazan National Research Technological University
														Email: ysamuilov@yandex.ru
				                	ORCID iD: 0000-0001-7763-8326
				                																			                												                	Ресей, 							Kazan, 420015						
E. Kozhanova
Kazan National Research Technological University
														Email: ysamuilov@yandex.ru
				                	ORCID iD: 0009-0004-6676-9629
				                																			                												                	Ресей, 							Kazan, 420015						
Y. Samuilov
Kazan National Research Technological University
							Хат алмасуға жауапты Автор.
							Email: ysamuilov@yandex.ru
				                	ORCID iD: 0000-0002-5943-7448
				                																			                												                	Ресей, 							Kazan, 420015						
Әдебиет тізімі
- Polyurea: Synthesis, Properties, Composites, Production, and Applications / Eds. P. Pasbakhsh, D. Mohotti, K. Palaniandy, Sh. Ambarine, B. Auckloo. Amsterdam: Elsevier, 2023. 430 p.
- Toader G., Rusen E., Teodorescu M., Diacon A., Stanescu P.O., Rotariu T., Rotariu A. // J. Appl. Polym. Sci. 2016. Vol. 133. N 38. P. 43967. doi: 10.1002/app.43967
- Zhang R., Huang W., Lyu P., Yan S., Wang X., Ju J. // Polymers. 2022. Vol. 14. N 13. P. 2670. doi: 10.3390/polym14132670
- Wu G., Wang X., Wang Y., Ji C., Zhao C. // Mater. Des. 2022. Vol. 224. P. 111371. doi 10.1016/ j.matdes.2022.111371
- Luo Y., Pu K., Gao J., Zhou Y., Wan J., Bai X. // J. Appl. Polym. Sci. 2024. Vol. 141. N 18. P. e55304. doi: 10.1002/app.55304
- Lai W., Qin B., Xu J.F., Zhang X. // J. Polym. Sci. 2024. Vol. 62. N 5. P. 900. doi: 10.1002/pol.20230455
- Luo J., Wang T., Sim C., Li Y. // Polymers. 2022. Vol. 14. N 14. P. 2808. doi: 10.3390/polym14142808
- Toader G., Diacon A., Axinte S.M., Mocanu A., Rusen E. // Polymers. 2024. Vol. 16. N 4. P. 454. doi: 10.3390/polym16040454
- Iqbal N., Kumar D., Roy P.K. // J. Appl. Polym. Sci. 2018. Vol. 135. N 40. P. 46730. doi: 10.1002/app.46730
- Isocyanates: Sampling, Analysis, and Health Effects / Eds. J. Lesage, I. DeGraff, R. Danchik. West Conshohocken: ASTM International, 2001. 133 p.
- Shi R., Jiang S., Cheng H., Wu P., Zhang C., Arai M., Zhao F. // ACS Sust. Chem. Eng. 2020. Vol. 8. N 50. P. 18626. doi: 10.1021/acssuschemeng.0c06911
- Lin C., Xie K., Tang D. // J. Appl. Polym. Sci. 2022. Vol. 139. N 28. P. e52513. doi: 10.1002/app.52513
- Zheng L., Xi Q., Hu G., Wang B., Song D., Zhang Y., Liu Y. // Polymers. 2024. Vol. 16. N 7. P. 993. doi: 10.3390/polym16070993
- Tundo P., Arico F. // ChemSusChem. 2023. Vol. 16. N 23. P. e202300748. doi: 10.1002/cssc.202300748
- Verma K., Sharma A., Singh J., Badru R. // Sustain. Chem. Pharm. 2023. Vol. 33. P. 101117. doi 10.1016/ j.scp.2023.101117
- Самуилов А.Я., Алекбавев Д.Р., Самуилов Я.Д. // ЖOpХ. 2018. Т. 54. № 10. С. 1441; Samuilov A.Y., Alekbaev D.R., Samuilov Y.D. // Russ. J. Org. Chem. 2018. Vol. 54. N 10. P. 1453. doi: 10.1134/S1070428018100032
- Самуилов А.Я., Самуилов Я.Д. // ЖФХ. 2022. Т. 96. № 2. С. 205; Samuilov A.Y., Samuilov Y.D. // Russ. J. Phys. Chem. (A). 2022. Vol. 96. N 2. P. 293. doi: 10.1134/S0036024422020248
- Ma S., Liu C., Sablong R.J., Noordover B.A., Hensen E.J., van Benthem R.A., Koning C.E. // ACS Catal. 2016. Vol. 6. N 10. P. 6883. doi: 10.1021/acscatal.6b01673
- Ban J.L., Li S.Q., Yi C.F., Zhao J.B., Zhang Z.Y., Zhang J.Y. // Chin. Polym. Sci. 2019. Vol. 37. P. 43. doi: 10.1007/s10118-018-2165-0
- Rhoné B., Semetey V. // Synlett. 2017. Vol. 28. N 15. P. 2004. doi: 10.1055/s-0036-1588866
- Zhao L., Semetey V. // ACS Omega. 2021. Vol. 6. N 6. P. 4175. doi: 10.1021/acsomega.0c04855
- Bakkali-Hassani C., Berne D., Ladmiral V., Caillol S. // Macromolecules. 2022. Vol. 55. N 18. P. 7974. doi: 10.1021/acs.macromol.2c01184
- Alam M.M., Varala R., Seema V. // Mini-Rev. Org. Chem. 2024. Vol. 21. N 5. P. 555. doi: 10.2174/1570193X20666230507213511
- Kožený V., Mindl J., Štěrba V. // Chem. Pap. 1997. Vol. 51. N 1. P. 29.
- Prachi R., Tanwar D.K., Gill M.S. // SynOpen. 2023. Vol. 7. N 4. P. 555. doi: 10.1055/a-2157-5925
- Ohshima T., Hayashi Y., Agura K., Fujii Y., Yoshiyama A., Mashima K. // Chem. Commun. 2012. Vol. 48. N 44. P. 5434. doi: 10.1039/c2cc32153j
- Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Scalmani G., Barone V., Mennucci B., Petersson G.A., Nakatsuji H., Caricato M., Li X., Hratchian H.P., Izmaylov A.F., Bloino J., Zheng G., Sonnenberg J.L., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Vreven T., Montgomery J.A., Jr., Peralta J.E., Ogliaro F., Bearpark M., Heyd J.J., Brothers E., Kudin K.N., Staroverov V.N., Keith T., Kobayashi R., Normand J., Raghavachari K., Rendell A., Burant J.C., Iyengar S.S., Tomasi J., Cossi M., Rega N., Millam J.M., Klene M., Knox J.E., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Martin R.L., Morokuma K., Zakrzewski V.G., Voth G.A., Salvador P., Dannenberg J.J., Dapprich S., Daniels A.D., Farkas Ö., Foresman J.B., Ortiz J.V., Cioslowski J., Fox D.J. Gaussian 09. Revision A.1. Gaussian Inc, Wallingford, 2009.
- Sholl D.S., Steckel J.A. Density Functional Theory: A Practical Introduction. Hoboken: John Wiley & Sons, 2023. 224 p.
- Density Functional Theory: Modeling, Mathematical Analysis, Computational Methods, and Applications / Eds. E. Cancès, G. Friesecke. Cham: Springer, 2023. 580 p.
- Wynne‐Jones W.F.K., Eyring H. // J. Chem. Phys. 1935. Vol. 3. N 8. P. 492. doi: 10.1063/1.1749713
Қосымша файлдар
 
				
			 
						 
					 
						 
						 
						












