Synthesis and physicochemical properties of tin(IV), zirconium(IV), and hafnium(IV) 2(3),9(10),16(17),23(24)-tetrakis-(4-tritylphenoxy)phthhalocyaninates

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Resumo

The reaction of 4-tritylphenoxyphthalonitrile with SnCl2, ZrCl4 and HfCl4 in the presence of urea under ammonium molybdate catalysis was used to synthesize tetrakis-(4-tritylphenoxy)phthalocyaninates of tin(IV), zirconium(IV), and hafnium(IV). The complexes were characterized by spectral methods of analysis, including mass spectrometry, 1Н NMR, vibrational and electron spectroscopy. All of them form J -type dimer associates in chloroform at concentrations up to ~1.5×10-6 mol/L and lower, are not associated in a mixture of toluene and pyridine up to concentrations of ~3×10-5 mol/L and higher, have catalytic activity in electroreduction reactions of molecular oxygen. The complexes of zirconium and hafnium showed the highest activity. Tin and zirconium complexes are thermally stable in an inert atmosphere up to a temperature of 200°C.

Sobre autores

T. Rumyantseva

Ivanovo State University of Chemistry and Technology

M. Bazanov

Ivanovo State University of Chemistry and Technology

N. Galanin

Ivanovo State University of Chemistry and Technology

Email: galanin_ne@isuct.ru

Bibliografia

  1. Yuan S., Peng J., Zhang Y., Zheng D.J., Bagi S., Wang T., Roman-Leshkov Y., Shao-Horn Y. // ACS Catal. 2022. Vol. 12. N 12. P. 7278. doi: 10.1021/acscatal.2c00184
  2. Dickerson S.D., Ayare P.J., Vannucci A.K., Wiskur S.L. // J. Photochem. Photobiol. (A). 2022. Vol. 422. 113547. doi: 10.1016/j.jphotochem.2021.113547
  3. Usol'tseva N.V., Kazak A.V., Luk'yanov I.Yu., Sotsky V.V., Smirnova A.I., Yudin S.G., Shaposhnikov G.P., Galanin N.E. // Phase Trans. 2014. Vol. 87. N 8. P. 801. doi: 10.1080/01411594.2014.893343
  4. Peng J., Li X., Liu Y., Zhuge W., Zhang C., Huang Y. // Sensors and Actuators (B). 2022. Vol. 360. 131619. doi: 10.1016/j.snb.2022.131619
  5. Yahya M., Nural Y., Seferoglu Z. // Dyes Pigm. 2022. Vol. 198. Article no.109960. doi: 10.1016/j.dyepig.2021.109960
  6. Urbani M., Ragoussi M.-E., Nazeeruddin M.K., Torres T. // Coord. Chem. Rev. 2019. Vol. 381. P. 1. doi: 10.1016/j.ccr.2018.10.007
  7. Znoiko S.A., Elizarova A.P., Kustova T.V., Nakonechnaya A.N. // Chem.Chem.Tech. 2021. Vol. 64. N 4. P. 42. doi: 10.6060/ivkkt.20216404.6380
  8. Solgun D.G., Horoz S., Agirtas M.S. // Inorg. Nano-Met. Chem. 2018. Vol. 48. N 10. P. 508. doi: 10.1080/24701556.2019.1572624
  9. Usol'tseva N., Bykova V., Ananjeva G., Zharnikova N., Kudrik E. // Mol. Cryst. Liq. Cryst. 2004. Vol. 411. N 1. P. 329. doi: 10.1080/15421400490435350
  10. Zharnikova N., Usol'tseva N., Kudrik E., Thelakkat M. // J. Mater. Chem. 2009. Vol. 19. N 20. P. 3161. doi: 10.1039/b821306b
  11. Tretyakova I.N., Chernii V.Ya., Tomachynski L.A., Volkov S.V. // Dyes and Pigments. 2007. Vol. 75. N 1. P. 67. doi: 10.1016/j.dyepig.2006.05.013
  12. Chernii V.Ya., Bon V.V., Tretyakova I.N., Severinovskaya O.V., Volkov S.V. // Dyes and Pigments. 2012. Vol. 94. N 2. P. 187. doi: 10.1016/j.dyepig.2011.12.012
  13. Gerasymchuk Y.S., Chernii V.Ya., Tomachynski L.A., Legendziewicz J., Radzki S. // Opt. Mater. 2005. Vol. 27. N 9. P. 1484. doi: 10.1016/j.optmat.2005.01.013
  14. Obaidulla S.M., Goswami D.K., Giri P.K. // Appl. Phys. Lett. 2014. Vol. 104. N 21. Article no. 213302. doi: 10.1063/1.4879015
  15. Song D., Wang H., Zhu F., Yang J., Tian H., Geng Y., Yan D. // Adv. Mater. 2008. Vol. 20. N 11. P. 2142. doi: 10.1002/adma.200702439
  16. Zhao Y., Qi S., Niu Z., Peng Y., Shan C., Verma G., Wojtas L., Zhang Z., Zhang B., Feng Y., Chen Y.-S., Ma S. // J. Am. Chem. Soc. 2019. Vol. 141. N 36. P. 14443. doi: 10.1021/jacs.9b07700
  17. Lv N., Li Q., Zhu H., Mu S., Luo X., Ren X., Liu X., Li S., Cheng C., Ma T. // Adv. Sci. 2023. Vol. 10. N 7. P. 2206239. doi: 10.1002/advs.202206239
  18. Tverdova N.V., Giricheva N.I., Maizlish V.E., Galanin N.E., Girichev G.V. // Int. J. Mol. Sci. 2022. Vol. 23. N 22. 13922. doi: 10.3390/ijms232213922
  19. Kroenke W.J., Kenney M.E. // Inorg. Chem. 1964. Vol. 3. N 2. P. 251. doi: 10.1021/ic50012a025
  20. Barrett P.A., Dent C.E., Linstead R.P. // J. Chem. Soc. 1936. P. 1719. doi: 10.1039/JR9360001719
  21. Tolbin A.Yu., Dzuban A.V., Shestov V.I., Gudkova Y.I., Brel V.K., Tomilova L.G., Zefirov N.S. // RSC Adv. 2015. Vol. 5. N 11. P. 8239. doi: 10.1039/c4ra15239e
  22. Tolbin A.Yu., Sheinin V.B., Koifman O.I., Tomilova L.G. // Macroheterocycles. 2015. Vol. 8. N 2. P. 150. doi: 10.6060/mhc150454t
  23. Tolbin A.Yu., Pushkarev V.E., Balashova I.O., Dzuban A.V., Tarakanov P.A., Trashin S.A., Tomilova L.G., Zefirov N.S. // New J. Chem. 2014. Vol. 38. N 12. P. 5825. doi: 10.1039/c4nj00692e
  24. Huang X., Zhao F., Li Z., Tang Y., Zhang F., Tung C.-H. // Langmuir. 2007. Vol. 23. N 9. P. 5167. doi /10.1021/la062326c
  25. Berezina N.M., Klueva M.E., Bazanov M.I. // Macroheterocycles. 2017. Vol. 10. N 3. P. 308. doi: 10.6060/mhc170507b
  26. Petrova D.V., Semeikin A.S., Berezina N.M., Berezin M.B., Bazanov M.I. // Macroheterocycles. 2019. Vol. 12. N 2. P. 119. doi: 10.6060/mhc190553s
  27. Do Ngoc Minh, Berezina N.M., Bazanov M.I., Semeikin A.S., Glazunov A.V. // Macroheterocycles. 2015. Vol. 8. N 1. P. 56. doi: 10.6060/mhc140714b
  28. Филимонов Д.А., Алексеева С.В., Базанов М. И., Койфман О.И., Кокорин М.С. // Макрогетероциклы. 2018. Т. 11. № 1. С. 52. doi: 10.6060/mhc151204b
  29. Peterson M., Hunt C., Wang Z., Heinrich S.E., Wu G., Menard G. // Dalton Trans. 2020. Vol. 49. N 45. P. 16268. doi: 10.1039/D0DT01372B
  30. Sakamoto K, Ohno-Okumura E, Kato T, Soga H. // J. Porph. Phthal. 2010. Vol. 14. N 1. P. 47. doi: 10.1142/S1088424610001726
  31. Farajzadeh N., Akyüz D., Koca A., Kocak M.B. // Polyhedron. 2020. Vol. 177. Article no. 114264. 10.1016/j.poly.2019.114264
  32. Omeroglu I., Biyiklioglu Z. // Turk. J. Chem. 2015. Vol. 39. N 2. P. 347. doi: 10.3906/kim-1408-71
  33. Ou Z., Zhan R., Tomachynski L.A., Chernii V.Ya., Kadish K.M. // Macroheterocycles. 2011. Vol. 4. N 3. P. 164.
  34. Базанов М.И., Петров А.В., Жутаева Г.В., Турчанинова И.В., Андриевски Г., Евсеев А.А. // Электрохимия. 2004. Т. 40. № 11. С. 1396
  35. Bazanov M.I., Petrov A.V., Zhutaeva G.V., Turchaninova I.V., Andrievski G., Evseev A.A. // Russ. J. Electrochem. 2004. Vol. 40. N 11. P. 1198. doi: 10.1023/B:RUEL.0000048654.68212.1e

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