Email this article 
Deactivation of triplet states of the metalloporphyrins by molecular oxygen
- Authors: Starukhin A.S.1, Ilyin A.Y.1, Pavich T.A.1
-
Affiliations:
- B.I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus
- Issue: Vol 88, No 6 (2024)
- Pages: 929-934
- Section: Quantum Optics and Coherent Spectroscopy
- URL: https://jdigitaldiagnostics.com/0367-6765/article/view/654660
- DOI: https://doi.org/10.31857/S0367676524060136
- EDN: https://elibrary.ru/PGXGHB
- ID: 654660
Cite item
Open Access
Access granted
Abstract
The values of the phosphorescence decay time of the metalloporphyrins upon selective excitation into the absorption bands and the atmospheric concentration of molecular oxygen in solution has been recorded at 293 K. It was demonstrated that the decay time of triplet states depends on the polarity of the solvents, as well as on the wavelength of the excitation.
Full Text
About the authors
A. S. Starukhin
B.I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus
Author for correspondence.
Email: a.starukhin@ifanbel.bas-net.by
Belarus, Minsk
A. Yu. Ilyin
B.I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus
Email: a.starukhin@ifanbel.bas-net.by
Belarus, Minsk
T. A. Pavich
B.I. Stepanov Institute of Physics of the National Academy of Sciences of Belarus
Email: a.starukhin@ifanbel.bas-net.by
Belarus, Minsk
References
- Gu J., Peng Y., Zhou T. et al. // Nano Res. Energy. 2022. V. 1. Art. No e9120009.
- Park J., Lee J., Jang W. // Coord. Chem. Rev. 2020. V. 407. No. 4. Р. 213157.
- Park J., Hong K., Lee H. et al. // Acc. Chem. Res. 2021. V. 54. No. 9. Р. 2249.
- Shi Y., Zhang F., Linhardt R. // Dyes Pigments. 2021. V. 188. Art. No. 109136.
- Старухин А.С., Павич Т.А., Романенко А.А. и др. // Изв. РАН. Сер. физ. 2022. Т. 86. № 6. С. 781; Starukhin A.S., Pavich T.A., Ramanenka A.A. et. al // Bull. Russ. Acad. Sci. Phys. 2022. V. 86. No. 6. Р. 655.
- Marian C. // Advanced Review. 2012. V. 2. No. 2. Р. 187.
- Darwent J., Douglas P., Harriman A. et al. // Coord. Chem. Rev. 1982. V. 4. No. 6. P. 83.
- Uhl R., Meyer B., Desel H. // J. Biochem. Biophys. Meth. 1984. V. 10. No. 1—2. P. 35.
- Джагаров Б.М., Салохиддинов К.И. // Опт. и спектроск. 1981. Т. 51. № 5. С. 841.
- Джагаров Б.М., Гуринович Г.П., Новиченков В.Е. и др. // Xим. физика. 1987. T. 6. № 5. С. 1069.
- Старухин А.С., Панарин А.Ю. // Журн. прикл. спектроск. 2023. Т. 90. № 5. С. 747; Starukhin A.S., Panarin A.Yu. // J. Appl. Spectrosc. 2023. V. 90. Nо. 5. Р. 1037.
- Sakamoto K., Ohno-Okumura E. // Materials. 2009. V. 2. Nо. 3. Р. 1127.
- Sessler J., Mozaffari А., Johnson A. // Organic Syntheses. 2003. V. 70. Р. 68.
- Старухин А.С., Романенко А.А., Плавский В.Ю. // Опт. и спектроск. 2022. Т. 130. № 5. С. 709; Statrukhin A.S., Romanenko A.A., Plavskii V.Yu. // Opt. Spectrosc. 2022. V. 130. No. 5. P. 319.
- Старухин А.С., Павич Т.А., Романенко А.А. и др. // Изв. РАН. Сер. физ. 2022. Т. 86. № 6. С. 781; Starukhin A.S., Korol Yu.D., Pavich A.A. et al. // Bull. Russ. Acad. Sci. Phys. 2022. V. 86. No. 6. Р. 650.
- Smith G.J. // J. Chem. Soc. Fаraday Trans. 1982. V. 78. No. 2. Р. 769.
- Zhan X., Lee W., Sudhakar L.K. et al. // Inorg. Chem. 2021. V. 60. No. 6. P. 8442.
- Darmanyan A.P. // Chem. Phys. Lett. 1983. V. 96. No. 3. P. 383.
- Montalti M., Credi A., Prodi L., Gandolfi M. // In: Handbook of photochemistry. Materials science. Boca Raton: SRC, Taylor & Francis Group, 2006. P. 542.
- Harriman A. // J. Chem. Soc. Faraday Trans. 1981. V. 77. No. 7. P. 1281.
- Ганжа В.А., Гуринович Г.П., Джагаров Б.М. и др. // Журн. прикл. спектроск. 1989. Т. 50. № 4. С. 618; Ganzha V.A., Gurinovich G.P., Dzhagarov B.M. et al. // J. Appl. Spectrosc. 1989. V. 50. Nо. 4. Р. 402.
Supplementary files
