Oxidation of the Styrene Epoxide – Hydroquinone – Copper(II) Chloride Ternary System in a Methanol Solution
- Авторлар: Petrov L.V.1, Solyanikov V.M.1
-
Мекемелер:
- Federal Research Center for Problems of Chemical Physics and Medical Chemistry of the Russian Academy of Sciences
- Шығарылым: Том 43, № 9 (2024)
- Беттер: 53-60
- Бөлім: Kinetics and mechanism of chemical reactions, catalysis
- URL: https://gynecology.orscience.ru/0207-401X/article/view/680966
- DOI: https://doi.org/10.31857/S0207401X24090062
- ID: 680966
Дәйексөз келтіру
Аннотация
The consumption of styrene epoxide (SE) and hydroquinone (HQ) in a ternary TrS system (SE – HQ – Cu(II)) in an oxygen atmosphere in a methanol solution was studied. Oxygen uptake by the triple system SE – HQ – CuCl2 was studied manometrically. Expression of velocity in terms of reagent concentrations V = k [Cu(II)]1 [HQ]0 [SE]0, the effective oxidation rate constant k = 1.82×105 exp(– 40 kJ mol-1/RT) s-1, (308–323) K. The mechanism of oxidation of TrS is discussed.
Негізгі сөздер
Толық мәтін

Авторлар туралы
L. Petrov
Federal Research Center for Problems of Chemical Physics and Medical Chemistry of the Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: plv@acp.ac.ru
Ресей, Chernogolovka
V. Solyanikov
Federal Research Center for Problems of Chemical Physics and Medical Chemistry of the Russian Academy of Sciences
Email: plv@acp.ac.ru
Ресей, Chernogolovka
Әдебиет тізімі
- Ch. Schneider, Synthesis 23, 3919 (2006). https://doi.org/ 10.1055/s-2006-950348
- G. Sabitha, R. Satheesh Babu, M. Rajkumar, Ch. Srinivas Reddy, J.S. Yadav, Tetrahedron Lett. 42, 3955 (2001). https://doi.org/10.1016/S0040-4039(01)00622-0
- Y.-X. Zhou, Y.-Z. Chen, Y. Hu, G. Huang, S.-H. Yu, H.-L. Jiang, Chem. Eur. J. 20, 1 (2014). https://doi.org/ 10.1002/chem. 201404104
- Y. Zhang, M. Wang, P. Li, L. Wang, Org. Lett. 14, 2206 (2012). https://doi.org/10.1021/o1300391t
- D.A. Denisov, R.A. Novikov, Y.V. Tomilov, Russ. Chem. Bull. 70, 1568 (2021). https://doi.org/10.1007/S11172-021-3253-9
- R.E. Parker, N.S. Isaacs, Chem. Rev. 53, 737 (1959). https://doi.org/10.1021/cr50028a006
- A.M. Ross, T.M. Pohl, K. Piazza, M. Thomas, B. Fox, D.L. Whalen, J. Am. Chem. Soc. 104, 1658 (1982). https://doi.org/10.1021/ja00370a035
- A. Lundin, I. Panas, E. Ahlberg, J. Phys. Chem. A 111, 9087 (2007). https://doi.org/10.1021/jp073285b
- P.O. Wennberg, D.G. VanderVelde, N.C. Eddingsaas, J. Phys. Chem. A 114, 8106 (2010). https://doi.org/10.1021/jp103907c
- Z. Huan, Ch. Yung, Z. Ma, E.R. Gainer, D. Li, J. Phys. Chem. A 118, 1557 (2014). https://doi.org/10.1021/jp501310z
- L.V. Petrov, V.M. Solyanikov, Russ. Chem. Bull. 64, 107 (2015).
- L.V. Petrov, V.M. Solyanikov, Russ. J. Phys. Chem. B 10, 764 (2016). https://doi.org/10.1134/S1990793116050225
- L.V. Petrov, V.M. Solyanikov, Pet. Chem. 57, 734 (2017). https://doi.org/10.1134/S0965544117080114
- L.V. Petrov, V.M. Solyanikov, Russ. J. Phys. Chem. B 12, 1003 (2018). https://doi.org/10.1134/S1990793118060179
- L.V. Petrov, V.M. Solyanikov, Russ. Chem. Bull. 69, 1869 (2020). https://doi.org/10.1007/S11172-020-2972-7
- L.V. Petrov, V.M. Solyanikov, Russ. J. Phys. Chem. B 15, 599 (2021). https://doi.org/10.1134/S1990793121040084
- V.A. Menshov, V.D. Kancheva, O.L. Yablonskaya, A.V. Trofimov, Russ. J. Phys. Chem. B 15, 108 (2021). https://doi.org/10.1134/S1990793121010231
- I.F. Rusina, T.L. Veprintsev, R.F. Vasil’ev, Russ. J. Phys. Chem. B 16, 50 (2022). https://doi.org/10.1134/S1990793122010274
- L.V. Petrov, V.M. Solyanikov, Russ. J. Phys. Chem. B 15, 960 (2021). https://doi.org/10.1134/S1990793121060075
- L.V. Petrov, B. L. Psikha, V.M. Solyanikov, Pet. Chem. 49, 263 (2009).
- L.V. Petrov, V.M. Solyanikov, Pet. Chem. 39, 107 (1999).
- L.V. Petrov, V.M. Solyanikov, Russ. J. Phys. Chem. B 17, 1259 (2023). https://doi.org/10.1134/S1990793123060234
Қосымша файлдар
