Статья
2021
Synthesis and Photocatalytic Properties of Magnesium Silicate Modified with Cationic Chlorin e6 Derivatives
I. V. Loukhina, M. A. Gradova, I. S. Khudyaeva, А. V. Lobanov, D. V. Belykh
Российский журнал общей химии
https://doi.org/10.1134/S1070363221040198
Abstract / Full Text
Synthetic samples of layered magnesium silicate modified with mono-, di-, and tricationic chlorin е6 derivatives have exhibited comparable photochemical activity towards a series of reductants: 1,3-diphenylisobenzofuran selectively oxidizable with singlet oxygen and 1,2-phenylenediamine readily oxidizable with hydrogen peroxide. The optimal photochemical activity of the modified magnesium silicates has been achieved at the ratio of 4–8 μmol of chlorin e6 derivative per 1 g of magnesium silicate.
Author information
- Institute of Chemistry of Komi Science Centre of the Ural Branch of the Russian Academy of Sciences, 167000, Syktyvkar, RussiaI. V. Loukhina, I. S. Khudyaeva & D. V. Belykh
- N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, 119991, Moscow, RussiaM. A. Gradova & А. V. Lobanov
References
- Abrahamse, H. and Hamblin, M.R., Biochem. J., 2016, vol. 473, p. 347. https://doi.org/10.1042/BJ20150942
- Kwiatkowski, S., Knap, B., Przystupski, D., Saczko, J., Kędzierska, E., Knap-Czop, K., Kotlińska, J., Michel, O., Kotowski, K., and Kulbacka, J., Biomed. Pharmacother., 2018, vol. 106, p. 1098. https://doi.org/10.1016/j.biopha.2018.07.049
- McFarland, S.A., Mandel, A., Dumoulin-White, R., and Gasser, G., Curr. Opin. Chem. Biol., 2020, vol. 56, p. 23. https://doi.org/10.1016/j.cbpa.2019.10.004
- Wozniak, A. and Grinholc, M., Front. Microbiol., 2018, vol. 9, p. 930. https://doi.org/10.3389/fmicb.2018.00930
- Soares, J.M., Corrêa, T.Q., Inada, N.M., Bagnato, V.S., and Blanco, K.C., J. Pharm. Pharmacol., 2018, vol. 6, p. 863. https://doi.org/10.17265/2328-2150/2018.09.009
- Moura, N.M.M., Esteves, M., Vieira, C., Rocha, G.M.S.R.O., Faustino, M.A.F., Almeida, A., Cavaleiro, J.A.S., Lodeiro, C., and Neves, M.G.P.M.S., Dyes Pigm., 2019, vol. 160, p. 361. https://doi.org/10.1016/j.dyepig.2018.06.048
- Sobotta, L., Sniechowska, J., Ziental, D., Dlugaszewska, J., and Potrzebowski, M.J., Dyes Pigm., 2019, vol. 160, p. 292. https://doi.org/10.1016/j.dyepig.2018.08.004
- Demel, J. and Lang, K., Eur. J. Inorg. Chem., 2012, p. 5154. https://doi.org/10.1002/ejic.201200400
- Walter, M.G., Rudine, A.B., and Wamser, C.C., J. Porphyrins Phthalocyanines, 2010, vol. 14, p. 759. https://doi.org/10.1142/S1088424610002689
- Urbani, M., Grätzel, M., Nazeeruddin, M.K., and Torres, T., Chem. Rev., 2014, vol. 114, no. 24, p. 12330. https://doi.org/10.1021/cr5001964
- Calmeiro, J.M.D., Gira, G., Ferraz, F.M., Fernandes, S.R.G., Pinto, A.L., Lourenço, L.M.O., Tome, J.P.C., and Pereira, C.C.L., Dyes Pigm., 2020, vol. 177, p. 108280. https://doi.org/10.1016/j.dyepig.2020.108280
- Matsuo, Y., Ogumi, K., Jeon, I.J., Wang, H., and Nakagawa, T., RSC Adv., 2020, vol. 10, p. 32678. https://doi.org/10.1039/d0ra03234d
- Mathew, S., Yella, A., Gao, P., Humphry-Baker, R., Curchod, B.F., Ashari-Astani, N., Tavernelli, I., Rothlisberger, U., Nazeeruddin, M.K., and Grätzel, M., Nat. Chem., 2014, vol. 6, p. 242. https://doi.org/10.1038/NCHEM.1861
- Park, J.M., Lee, J.H., and Jang, W.-D., Coord. Chem. Rev., 2020, vol. 407, p. 213157. https://doi.org/10.1016/j.ccr.2019.213157
- Marin, M.L., Santos-Juanes, L., Arques, A., Amat, A.M., and Miranda, M.A., Chem. Rev., 2012, vol. 112, no. 3, p. 1710. https://doi.org/10.1021/cr2000543
- Nowakowska, M. and Szczubiałka, K., Polym. Degrad. Stab., 2017, vol. 145, p. 120. https://doi.org/10.1016/j.polymdegradstab.2017.05.021
- Ussia, M., Urso, M., Miritello, M., Bruno, E., Curcuruto, G., Vitalini, D., Condorelli, G.G., Cantarella, M., Privitera, V., and Carroccio, S.C., RSC Adv., 2019, vol. 9, p. 30182. https://doi.org/10.1039/c9ra06328e
- Regulska, E., Rivera-Nazario, D.M., Karpinska, J., Plonska-Brzezinska, M.E., and Echegoyen, L., Molecules, 2019, vol. 24, no. 6, p. 1118. https://doi.org/10.3390/molecules24061118
- Giannoudis, E., Benazzi, E., Karlsson, J., Copley, G., Panagiotakis, S., Landrou, G., Angaridis, P., Nikolaou, V., Matthaiaki, C., Charalambidis, G., Gibson, E.A., and Coutsolelos, A.G., Inorg. Chem., 2020, vol. 59, no. 3, p. 1611. https://doi.org/10.1021/acs.inorgchem.9b01838
- Ladomenou, K., Natali, M., Iengo, E., Charalampidis, G., Scandola, F., and Coutsolelos, A.G., Coord. Chem. Rev., 2015, vols. 304–305, p. 38. https://doi.org/10.1016/j.ccr.2014.10.001
- Nadeem, S., Mumtaz, A., Mumtaz, M., Mutalib, M.I.A., Shaharun, M.S., and Abdullah, B., J. Mol. Liq., 2018, vol. 272, p. 656. https://doi.org/10.1016/j.molliq.2018.09.077
- Amao, Y. and Kataoka, R., Catal. Today, 2018, vol. 307, p. 243. https://doi.org/10.1016/j.cattod.2017.12.029
- Tatsumi, D., Tsukamoto, T., Honna, R., Hoshino, S., Shimada, T., and Takagi, S., Chem. Lett., 2017, vol. 46, p. 1311. https://doi.org/10.1246/cl.170521
- Teramura, K., Tsuneoka, H., Ogura, K., Sugimoto, T., Shishido, T., and Tanaka, T., ChemCatChem., 2014, vol. 6, p. 2276. https://doi.org/10.1002/cctc.201402131
- Gurinovich, G.P., Sevchenko, A.N., and Solov’ev, K.N., Usp. Fiz. Nauk, 1963, vol. 79, no. 2, p. 173. https://doi.org/10.3367/UFNr.0079.196302a.0173
- Takagi, S., Shimada, T., Ishida, Y., Fujimura, T., Masui, D., Tachibana, H., Eguchi, M., and Inoue, H., Langmuir, 2013, vol. 29, p. 2108. https://doi.org/10.1021/la3034808
- Gradova, M.A., Ostashevskaya, I.I., Gradov, O.V., Lobanov, A.V., and Ivanov, V.B., Macroheterocycles, 2018, vol. 11, no. 4, p. 404. https://doi.org/10.6060/mhc181001g
- Dhital, B., Vishal, G.R., and Lu, H.P., Phys. Chem. Chem. Phys., 2017, vol. 19, p. 17216. https://doi.org/10.1039/C7CP01476G
- Won, D.-I., Lee, J.-S., Ba, Q., Cho, Y.-J., Cheong, H.-Y., Choi, S., Kim, C.H., Son, H.-J., Pac, C., and Kang, S.O., ACS Catal., 2018, vol. 8, p. 1018. https://doi.org/10.1021/acscatal.7b02961
- Eguchi, M., Shimada, T., Inoue, H., and Takagi, S., J. Phys. Chem. (C), 2016, vol. 120, no. 13, p. 7428. https://doi.org/10.1021/acs.jpcc.6b01211
- Tokieda, D., Tsukamoto, T., Ishida, Y., Ichihara, H., Shimada, T., and Takagi, S., J. Photochem. Photobiol. (A), 2017, vol. 339, p. 67. https://doi.org/10.1016/j.jphotochem.2017.01.013
- Grim, R.E., Clay Mineralogy, McGraw-Hill, 1953.
- Tarasevich, Yu.I., Stroenie i khimiya poverkhnosti sloistykh silikatov (Structure and Surface Chemistry of Layered Silicates), Kiev: Naukova dumka, 1988.
- Belykh, D., Loukhina, I., Mikhaylov, V., and Khudyaeva, I., Chem. Pap., 2020. https://doi.org/10.1007/s11696-020-01421-w
- Ogawa, M., Matsutomo, T., and Okada, T., J. Ceram. Soc. Japan, 2008, vol. 116, no. 12, p. 1309. https://doi.org/10.2109/jcersj2.116.1309
- Loukhina, I.V., Khudyaeva, I.S., Bugaeva, A.Yu., Dudkin, B.N., and Belykh, D.V., Russ. J. Gen. Chem., 2017, vol. 87, no. 5, p. 912. https://doi.org/10.1134/S1070363217050036
- Fujimura, T., Shimada, T., Hamatani, S., Onodera, S., Sasai, R., Inoue, H., and Takagi, S., Langmuir, 2013, vol. 29, no. 16, p. 5060. https://doi.org/10.1021/la4003737
- He, H., Frost, R.L., Bostrom, T., Yuan, P., Duong, L., Yang, D., Xi, Y., and Kloprogge, J.T., Appl. Clay. Sci., 2006, vol. 31, p. 262. https://doi.org/10.1016/j.clay.2005.10.011
- Carrado, K.A. and Winans, R.E., Chem. Mater., 1990, vol. 2, no. 3, p. 328. https://doi.org/10.1021/cm00009a027
- Loukhina, I.V., Khudyaeva, I.S., Bugaeva, A.Yu., and Belykh, D.V., Butlerovsk. Soobshch., 2019, vol. 58, no. 4, p. 34. https://doi.org/10.37952/ROI-jbc-01/19-58-4-34
- Gushchina, O.I., Larkina, E.A., and Mironov, A.F., Macroheterocycles, 2014, vol. 7, no. 4, p. 414. https://doi.org/10.6060/mhc140931g
- Tarabukina, I.S., Startseva, O.M., Patov, S.A., and Belykh, D.V., Macroheterocycles, 2015, vol. 8, no. 2, p. 168. https://doi.org/10.6060/mhc150456b
- Venediktov, E.A., Tulikova, E.Yu., Rozhkova, E.P., Khudyaeva, I.S., Belykh, D.V., and Berezin, D.B., Macroheterocycles, 2017, vol. 10, no. 3, p. 295. https://doi.org/10.6060/mhc170404v