Research Article
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Year 2019, , 46 - 51, 28.06.2019
https://doi.org/10.32571/ijct.543786

Abstract

References

  • 1. Mantareva, V.; Durmus, M.; Aliosman, M.; Stoineva I.; Angelov, I. Photodiagn. Photodyn. Ther. 2016, 14, 98-103.
  • 2. Duchi, S.; Ramos-Romero, S.; Dozza, B.; Guerra-Rebollo, M.; Cattini, L.; Ballestri, M.; Dambruoso, P.; Guerrini, A.; Sotgiu, G.; Varchi, G.; Lucarelli, E.; Blanco, J. Nanomedicine. 2016, 12, 1885-1897.
  • 3. Sfyri, G.; Kumar, C.V.; Wang, Y.L.; Xu, Z.X.; Krontiras C.A.; Lianosa, P. Appl. Surf. Sci. 2016, 360, 767 -771.
  • 4. Choi, S.A.; Kim, K.; Lee, S.J.; Lee, H.; Babajanyan, A.; Friedman, B.; Lee, K. J. Lumin. 2016, 171, 149-153.
  • 5. Ağırtaş, M.S. Inorg. Chim. Acta 2007, 360 (7), 2499-2502.
  • 6. McKeown, N.B. Phthalocyanines Materials–Synthesis, Structure and Functions, Cambridge University Press, Cambridge, 1998.
  • 7. Mele, G.; Annese, C.; Riccardis, A.D.; Fusco, C.; Palmisano, L.; Vasapollo G.; D’Accolti, L. Appl. Catal. A. 2014,481,169 -172.
  • 8. Ağırtaş¸ M.S.; Karatas¸ C.; Gümüs¸ S.; Okumus, V. Z. Anorg. Allg. Chem. 2015, 641 (2), 442 -447.
  • 9. Azzouzi, S.; Ali, M.B.; Abbas, M.N.; Bausells, J.; Zine N.; Errachid, A. Org. Electron. 2016, 34, 200-207.
  • 10. Medyouni, R.; Elgabsi, W.; Naouali, O.; Romerosa, A.; Al-Ayed, A.S.; Baklouti L.; Hamdi, N. Spectrochim. Acta, Part A. 2016, 167, 165-174.
  • 11. Ağırtaş, M.S. Dyes Pigments 2007, 74, 490-493.
  • 12. Ağırtaş¸ M.S.; Güven, M.E.; Gümüs, S.; Özdemir, S.; Dündar, A. Synthetic Met. 2014, 195, 177-184.
  • 13. Shaabani, A.; Keshipour, S.; Hamidzad, M.; Shaabani, S. J. Mol. Catal. A: Chem. 2014, 395, 494-499.
  • 14. Sevim, A.M.; Ilgün, C.; Gül, A. Dyes Pigments 2011, 89, 162-168.
  • 15. Cui, L.; Lv, G.; Dou, Z.; He, X. Electrochim. Acta 2013, 106, 272-278.
  • 16. Jasinski, R. Nature, 1964, 201, 1212-1213.
  • 17. Cabir, B.; Caner, N.; Yurderi, M., Kaya, M.; Agirtas, M.S.; Zahmakıran, M. Mater. Sci. Eng. B. 2017, 224, 9-17.
  • 18. Ebrahimian, A.; Zanjanchi, M.A.; Noei, H.; Arvand, M.; Wang, Y. J. Environ. Chem. Eng. 2014, 2, 484–494.
  • 19. Erickson, E.M.; Thorum, M.S.; Vasic, R.; Marinkovic, N.S.; Frenkel, A.I.; Gewirth A.A.; Nuzzo, R.G. J. Am. Chem. Soc. 2012, 134, 197-200.
  • 20. Armarego W.L.F.; Chai, C.L.L. Purification of laboratory Chemicals, 7nd ed., Butterwordh-Heinemann, Oxford, 2013.
  • 21. Liu, M.O.; Tai, C.H.; Wang, W.Y.; Chen, J.R.; Hu A.T.; Wei, T.H. J. Organomet. Chem. 2004, 689, 1078-1084.
  • 22. Snow, A.W.; Jarvis, N.L. J. Am. Chem. Soc. 1984, 106 (17), 4706-4711.
  • 23. Ağırtaş, M.S.; İzgi, M.S. J. Mol. Struct. 2009, 927, 126-128.
  • 24. Dilber, G, Durmuş, M; Kantekin, H. Dyes Pigments 2019,160, 267–284.
  • 25. Erdoğmus, A.; Arıcı, M. J. Fluorine Chem. 2014, 166, 127-133.
  • 26. Ağırtaş, M.S. Dyes Pigments 2008, 79, 247-251.
  • 27. Bartlett, M.A.; Mark, K.; Sundermeyer, J. Inorg. Chem. Commun. 2018, 98, 41–43.

Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method

Year 2019, , 46 - 51, 28.06.2019
https://doi.org/10.32571/ijct.543786

Abstract

In this study, zinc, cobalt and nickel phthalocyanine compounds bearing the 4-(2-phenylprop-2-yl)phenoxy) substituent were prepared. Here, a new practical method for synthesis was used. This method significantly shortens the synthesis time. This method is very effective for the reaction to take place in a short time and at a lower temperature. Additionally, these compounds were examined for their aggregation and photodegredation properties. The aggregation was studied in concentration range of 1x10-5-1x10-6 M in tetrahydrofuran (THF). The photodegradation properties of phthalocyanine complexes under light irradiation were also investigated in chloroform (CHCl3).

References

  • 1. Mantareva, V.; Durmus, M.; Aliosman, M.; Stoineva I.; Angelov, I. Photodiagn. Photodyn. Ther. 2016, 14, 98-103.
  • 2. Duchi, S.; Ramos-Romero, S.; Dozza, B.; Guerra-Rebollo, M.; Cattini, L.; Ballestri, M.; Dambruoso, P.; Guerrini, A.; Sotgiu, G.; Varchi, G.; Lucarelli, E.; Blanco, J. Nanomedicine. 2016, 12, 1885-1897.
  • 3. Sfyri, G.; Kumar, C.V.; Wang, Y.L.; Xu, Z.X.; Krontiras C.A.; Lianosa, P. Appl. Surf. Sci. 2016, 360, 767 -771.
  • 4. Choi, S.A.; Kim, K.; Lee, S.J.; Lee, H.; Babajanyan, A.; Friedman, B.; Lee, K. J. Lumin. 2016, 171, 149-153.
  • 5. Ağırtaş, M.S. Inorg. Chim. Acta 2007, 360 (7), 2499-2502.
  • 6. McKeown, N.B. Phthalocyanines Materials–Synthesis, Structure and Functions, Cambridge University Press, Cambridge, 1998.
  • 7. Mele, G.; Annese, C.; Riccardis, A.D.; Fusco, C.; Palmisano, L.; Vasapollo G.; D’Accolti, L. Appl. Catal. A. 2014,481,169 -172.
  • 8. Ağırtaş¸ M.S.; Karatas¸ C.; Gümüs¸ S.; Okumus, V. Z. Anorg. Allg. Chem. 2015, 641 (2), 442 -447.
  • 9. Azzouzi, S.; Ali, M.B.; Abbas, M.N.; Bausells, J.; Zine N.; Errachid, A. Org. Electron. 2016, 34, 200-207.
  • 10. Medyouni, R.; Elgabsi, W.; Naouali, O.; Romerosa, A.; Al-Ayed, A.S.; Baklouti L.; Hamdi, N. Spectrochim. Acta, Part A. 2016, 167, 165-174.
  • 11. Ağırtaş, M.S. Dyes Pigments 2007, 74, 490-493.
  • 12. Ağırtaş¸ M.S.; Güven, M.E.; Gümüs, S.; Özdemir, S.; Dündar, A. Synthetic Met. 2014, 195, 177-184.
  • 13. Shaabani, A.; Keshipour, S.; Hamidzad, M.; Shaabani, S. J. Mol. Catal. A: Chem. 2014, 395, 494-499.
  • 14. Sevim, A.M.; Ilgün, C.; Gül, A. Dyes Pigments 2011, 89, 162-168.
  • 15. Cui, L.; Lv, G.; Dou, Z.; He, X. Electrochim. Acta 2013, 106, 272-278.
  • 16. Jasinski, R. Nature, 1964, 201, 1212-1213.
  • 17. Cabir, B.; Caner, N.; Yurderi, M., Kaya, M.; Agirtas, M.S.; Zahmakıran, M. Mater. Sci. Eng. B. 2017, 224, 9-17.
  • 18. Ebrahimian, A.; Zanjanchi, M.A.; Noei, H.; Arvand, M.; Wang, Y. J. Environ. Chem. Eng. 2014, 2, 484–494.
  • 19. Erickson, E.M.; Thorum, M.S.; Vasic, R.; Marinkovic, N.S.; Frenkel, A.I.; Gewirth A.A.; Nuzzo, R.G. J. Am. Chem. Soc. 2012, 134, 197-200.
  • 20. Armarego W.L.F.; Chai, C.L.L. Purification of laboratory Chemicals, 7nd ed., Butterwordh-Heinemann, Oxford, 2013.
  • 21. Liu, M.O.; Tai, C.H.; Wang, W.Y.; Chen, J.R.; Hu A.T.; Wei, T.H. J. Organomet. Chem. 2004, 689, 1078-1084.
  • 22. Snow, A.W.; Jarvis, N.L. J. Am. Chem. Soc. 1984, 106 (17), 4706-4711.
  • 23. Ağırtaş, M.S.; İzgi, M.S. J. Mol. Struct. 2009, 927, 126-128.
  • 24. Dilber, G, Durmuş, M; Kantekin, H. Dyes Pigments 2019,160, 267–284.
  • 25. Erdoğmus, A.; Arıcı, M. J. Fluorine Chem. 2014, 166, 127-133.
  • 26. Ağırtaş, M.S. Dyes Pigments 2008, 79, 247-251.
  • 27. Bartlett, M.A.; Mark, K.; Sundermeyer, J. Inorg. Chem. Commun. 2018, 98, 41–43.
There are 27 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Articles
Authors

Mehmet Salih Ağırtaş 0000-0003-1296-2066

Cihan Durmuş This is me 0000-0001-8108-2404

Beyza Cabir This is me 0000-0003-4735-4511

Publication Date June 28, 2019
Published in Issue Year 2019

Cite

APA Ağırtaş, M. S., Durmuş, C., & Cabir, B. (2019). Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method. International Journal of Chemistry and Technology, 3(1), 46-51. https://doi.org/10.32571/ijct.543786
AMA Ağırtaş MS, Durmuş C, Cabir B. Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method. Int. J. Chem. Technol. June 2019;3(1):46-51. doi:10.32571/ijct.543786
Chicago Ağırtaş, Mehmet Salih, Cihan Durmuş, and Beyza Cabir. “Synthesis of Tetrakis (4-(2-Phenylprop-2-Yl) Phenoxy) Substituted Phthalocyanines Using a New Practical Method”. International Journal of Chemistry and Technology 3, no. 1 (June 2019): 46-51. https://doi.org/10.32571/ijct.543786.
EndNote Ağırtaş MS, Durmuş C, Cabir B (June 1, 2019) Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method. International Journal of Chemistry and Technology 3 1 46–51.
IEEE M. S. Ağırtaş, C. Durmuş, and B. Cabir, “Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method”, Int. J. Chem. Technol., vol. 3, no. 1, pp. 46–51, 2019, doi: 10.32571/ijct.543786.
ISNAD Ağırtaş, Mehmet Salih et al. “Synthesis of Tetrakis (4-(2-Phenylprop-2-Yl) Phenoxy) Substituted Phthalocyanines Using a New Practical Method”. International Journal of Chemistry and Technology 3/1 (June 2019), 46-51. https://doi.org/10.32571/ijct.543786.
JAMA Ağırtaş MS, Durmuş C, Cabir B. Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method. Int. J. Chem. Technol. 2019;3:46–51.
MLA Ağırtaş, Mehmet Salih et al. “Synthesis of Tetrakis (4-(2-Phenylprop-2-Yl) Phenoxy) Substituted Phthalocyanines Using a New Practical Method”. International Journal of Chemistry and Technology, vol. 3, no. 1, 2019, pp. 46-51, doi:10.32571/ijct.543786.
Vancouver Ağırtaş MS, Durmuş C, Cabir B. Synthesis of tetrakis (4-(2-phenylprop-2-yl) phenoxy) substituted phthalocyanines using a new practical method. Int. J. Chem. Technol. 2019;3(1):46-51.