Photochemical oxidation of water catalyzed by a cobalt (II) tetra-nuclear complex with polyoxovolphramophosphate ligands and lithium antications in artificial photosynthesis
- Авторлар: Dzhabieva Z.M.1, Ilyaschenko V.Y.1, Savinykh T.A.1, Dmitriev A.I.1, Zhidkov M.V.1, Baskakova Y.M.1, Dzhabiev T.S.1
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Мекемелер:
- Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
- Шығарылым: Том 59, № 1 (2025)
- Беттер: 46-52
- Бөлім: ФОТОКАТАЛИЗ
- URL: https://vietnamjournal.ru/0023-1193/article/view/684668
- DOI: https://doi.org/10.31857/S0023119325010064
- EDN: https://elibrary.ru/SPGMFR
- ID: 684668
Дәйексөз келтіру
Аннотация
Lithium salt of cobalt tetra-nuclear complex was synthesized and characterized by physicochemical methods Li10[Co4(H2O)2(α-PW9O34)2] 24H2O (1) – active homogeneous catalyst for the reaction of water oxidation with the formation of О2. ESI – mass spectrometric method shows the presence in the mass spectrum of the maximum peak with m/z = 1182.611 corresponding to the ion [Co4(PW9O34)2·HLi5]4– which forms a sandwich-type structure. Measurements of temperature-dependent magnetic susceptibility showed the predominance of antiferromagnetic interaction in the complex 1. The photochemical oxidation reaction of water under visible light irradiation in the presence of electron acceptor was studied Na2S2O8, photosensitizer bpy3RuCl2 and the catalyst. Efficiency of the catalytic system under optimal reaction conditions (рН 8, [1] = 5 μM), catalyst turnover number TON = 330, quantum yield of photogenerated oxygen (F = 0.46) is higher than that of the sodium salt of a similar catalyst (TON = 220, F = 0.27).
Авторлар туралы
Z. Dzhabieva
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Хат алмасуға жауапты Автор.
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
V. Ilyaschenko
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
T. Savinykh
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
A. Dmitriev
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
M. Zhidkov
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
Yu. Baskakova
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
T. Dzhabiev
Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry RAS
Email: dzhabiev@icp.ac.ru
Ресей, Chernogolovka
Әдебиет тізімі
- Джабиев Т.С., Шилов А.Е. // Успехи химии. 2012. Т. 81. № 12. С. 1146.
- Kärkäs M.D., Verho O., Jonston E.V., Åkermark B. // Chem. Rev. 2014. V. 114. P. 11863. https://doi.org/10.1021/cr400572
- Hurst J.K. // Science. 2010. V. 328. P. 315. https://doi.org/10.1126/science.1187721
- Yagi M., Kaneko M. // Chem. Rev. 2001. V. 101. P. 21. https://doi.org/10.1021/cr9801081
- Sens C., Romero I., Rodriguez M. et al. // J. Am. Chem.Soc. 2004. V. 126. P. 7798. https://doi.org/10.1021/ja0486824
- Suess-Fink G. // Angew. Chem. Int. Ed. 2008. V. 47. P. 5888. https://doi.org/10.1002/anie.200801121
- Gersten S.W., Samuels G.J., Meyer T.J. // J. Am. Chem. Soc. 1982. V. 104. P. 4029. https://doi.org/10.1021/ja00378a053
- Geletii Y. V., Botar B., Kogerler P. et. al // Angew. Chem. Int. Ed. 2008. V. 47. № 21. P. 3847. https://doi.org/10.1002/anie.200705652
- Sartorel A.; Carraro M.; Scorrano G. et al // J. Am. Chem. Soc. 2008. V. 130. P. 5006. https://doi.org/10.1021/ja0778371
- Geletii Y.V., Huang Z., Hou Y. et al // J. Am. Chem. Soc. 2009. V. 131. P. 7522. https://doi.org/10.1021/ja901373m
- Toma F. M.; Sartorel A.; Iurlo M. et al. //. Nat. Chem. 2010. V. 2. P. 826.
- Besson C., Huang Z., Geletii Y.V. et al. // Chem. Commun. 2010. V. 46. P. 2784. https://doi.org/10.1039/B926064A
- Murakami M., Hong D., Suenobu T. et al. // J. Am. Chem. Soc. 2011. V. 133. P. 11605.
- Zhu G., Geletii Y.V., Kogerler P. et al. // Dalton Trans. 2012. V. 41. P. 2084.
- Lv H., Geletii Y.V., Zhao C. et al. // Chem. Soc. Rev. 2012. V. 41. P. 7572.
- Sartorel A., Bonchio M., Campagna. S., Scandola, F. // Chem. Soc. Rev. 2014. V. 42. P. 2262. https://doi.org/10.1039/c2cs35287g
- Vickers J.W., Lv H., Sumliner J.M. et al. // J. Am. Chem. Soc. 2013. V. 135. P. 14110. https://doi.org/10.1021/ja4024868
- Sumliner J.M., Lv H., Fielden J. et al. // Eur. J. Inorg. Chem. 2014. V. 635.
- Vickers J.W., Sumliner J.M., Lv H. et al. // Phys. Chem. Chem. Phys. 2014. V. 16. P. 11942.
- Han X.-B., Zhang Z.-M., Zhang T. et al. // J. Am. Chem. Soc. 2014. V. 136. P. 5359.
- Шматко Н.Ю., Джабиева З.М. Химическое моделирование фермента, окисляющего воду в фотосистеме II. Фотокаталитические преобразователи солнечной энергии в энергию химических топлив. LAP LAMBERT Academic Publishing. Saarbrucken, Deutschland, 2012. 76 с. ISBN: 978-3-659-29482-2.
- Джабиева З.М., Ткаченко В.Ю., Джабиев Т.С. // Химия высоких энергий. 2017. Т. 51. № 3. С. 230; https://doi.org/10.7868/S0023119317030056
- Dzhabieva Z.M., Shilov G.V., Avdeeva L.V. et al. // Russian Journal of Inorganic Chemystry. 2024. P. 1. https://doi.org/10.1134/S0036023624601004
- Bi L.H., Huang R.D., Peng J. et al. // J. Chem. Soc. Dalton Trans. 2011. V. 121.
- Накамото К. Инфракрасные спектры неорганических и координационных соединений. М.: Мир. 1966. 411 с.
- Hatchard C.G., Parker C.A. // Proc. Roy Soc. London. 1956. V. A235. № 1203. P. 518.
- Yin Q., Tan J.M., Besson C. et al // Science. 2010. V. 328. P. 342.
- Bao Li, Yi Yan, Fengyan Li et al. // Inorganica Chimica Acta. 2009. V. 362. P. 2796.
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