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Journals / Türk Doğa ve Fen Dergisi / 2026 / Cilt: 14 Sayı: 2

Synthesis, Characterization and Investigation of Some Photophysical Properties of Novel Benzothiazole Based Pyridine Derivative

Hülya Elmalı Gülbaş(Uşak Üniversitesi)0000-0002-6041-6054
Pages
220–224
Publication Date
2025-06-27
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Benzothiazole substitute picolinoyl chloride derivate (BTPCP) has been shown fluorescence activity The novel fluorescence active BTPCP is expected to find application in especially sensor, different biological and pharmacological studies.

📌 3 Key Takeaways

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Objective & Hypothesis:Benzothiazole and its derivates have been play important role in chemical, biological and pharmacological reactions due to its heterocyclic structure.
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Key Findings & Data:In this study, fluorescent active novel benzothiazole substitute picolinoyl chloride derivate 6-((2-(benzothiazol-2 yl)phenyl)carbamoyl)picolinoyl chloride (BTPCP) successfully synthesized and characterized.
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Conclusion & Impact:Benzothiazole substitute picolinoyl chloride derivate (BTPCP) has been shown fluorescence activity The novel fluorescence active BTPCP is expected to find application in especially sensor, different biological and pharmacological studies.
🔬Design:Araştırma Makalesi
📍Scope:Comprehensive Sample
⚙️Variables:Benzotiyazol · Floresans Pikolinoil Klorür Türevi · Organik Sentez

Abstract

Benzothiazole and its derivates have been play important role in chemical, biological and pharmacological reactions due to its heterocyclic structure. In this study, fluorescent active novel benzothiazole substitute picolinoyl chloride derivate 6-((2-(benzothiazol-2 yl)phenyl)carbamoyl)picolinoyl chloride (BTPCP) successfully synthesized and characterized. Its structure was identified by classic spectroscopic methods (FT-IR, 1H-NMR and 13C-NMR). Its photophysical properties was investigated by using UV-Vis Spectrophotometer and Fluorescence Spectrophotometer. Benzothiazole substitute picolinoyl chloride derivate (BTPCP) has been shown fluorescence activity The novel fluorescence active BTPCP is expected to find application in especially sensor, different biological and pharmacological studies.

Özet

Benzotiyazol ve türevleri, heterosiklik yapıları nedeniyle kimyasal, biyolojik ve farmakolojik reaksiyonlarda önemli rol oynamaktadır. Bu çalışmada, floresan aktif yeni benzotiyazol substitue pikolinoil klorür türevi 6-((2-(benzotiyazol-2il)fenil)karbamoil)pikolinoil klorür (BTPCP) başarıyla sentezlenmiş ve karakterize edilmiştir. Sentezlenen BTPCP’nin molekül yapısı klasik spektroskopik yöntemler (FT-IR, 1H-NMR ve 13C-NMR) kullanılarak belirlenmiştir. BTPCP’nin fotofiziksel özellikleri Uv-Vıs Spektrofotometresi ve Flouresence Spektrofotometresi kullanılarak incelenmiştir. Yapılan incelemeler sonucunda benzotiyazol substitue pikolinoil klorür türevi BTPCP floresans aktivitesi gösterdiği belirlenmiştir. Yeni floresans aktif BTPCP'nin sensör çalışmaları başta olmak üzere, farklı biyolojik ve farmakolojik çalışmalarda uygulama bulması beklenmektedir.

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Cite This Article

Gülbaş, H. E. (2025). Synthesis, Characterization and Investigation of Some Photophysical Properties of Novel Benzothiazole Based Pyridine Derivative. Türk Doğa ve Fen Dergisi, Cilt: 14 Sayı: 2, 220–224. https://doi.org/10.46810/tdfd.1585498

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References (30)

  1. J.H. Wang, M. Li, D. Li, Chem. Sci. 4 (2013) 1793–1801.
  2. M.K. Amini, B. Khezri, A.R. Firooz, Sensor Actuat B-Chem. 131 (2008) 470–478.
  3. A.D. McFarland, R.P.V. Duyne, Nano Lett. 3 (2003) 1507–1511.
  4. H.S. Jung, M.S. Park, J.H. Han, J.H. Lee, C. Kang, J.H. Jung, J.S. Kim, Chem. Commun. 48 (2012) 5082–5084
  5. K.R. Dalton, M. J. Orr, A. J. Kwong, K. K. Deibler, H. H. Munshi, C. S. Bridges, T. J. Chen, X. Zhang, H. D. Lacorazza, K.A. Scheidt, ACS Medicinal Chemistry Letters 2023 14 (5), 606-613.
  6. J.P. Vacca, J.P. Maxwell, B. Williams, J.H. Come, S. Throner, World Intellectual Property Organization, WO2023064586 A1 2023-04-20 | Language: English, Database: Caplus ESPACENET
  7. J. Ling, J. Liu, World Intellectual Property Organization, WO2014183300 A1 2014-11-20 | Language: English, Database: CAplus ESPACENET
  8. Ge, H. Zhang, P. Wang, Chem. Soc. Rev. 40 (2011) 3483–3495; L.-J. Fan, Y. Zhang, C.B. Murphy, S.E. Angell, M.F.L. Parker, B.R. Flynn, W.E. Jones Jr., Coord. Chem. Rev. 253 (2009) 410–422.
  9. E. Hrishikesan, C. Saravanan, P. Kannan, Ind. Eng. Chem. Res. 50 (2011) 8225– 8229.
  10. J. Chan, S.C. Dodani, C.J. Chang, Nat. Chem. 4 (2012) 973–984.
  11. Q. Zou, H. Tian, Sensor Actuat. B-Chem. 149 (2010) 20–27.
  12. X. Zhang, Y. Shiraishi, T. Hirai, Tetrahedron Lett. 48 (2007) 5455–5459.
  13. A. Misra, M. Shahid, J. Phys. Chem. C 114 (2010) 16726–16739.
  14. H. E. Gülbaş, S. Bozkurt, E. Halay, J. Heterocycl. Chem. 2023, 60(7), 1223.
  15. O. A. Bozdemir, R. Guliyev, O. Buyukcakir, S. Selcuk, S. Kolamen,G. Gulseren, D. Nalbantoglu, H. Boyaci, E.U. Akkaya, Journal of the American Chemical Society, 132 (2010), 8029-8036.
  16. F.D. Natale, A. Lancia, A. Molino, M.D. Natale, D. Karatza, D. Musmarra, J. Hazard. Mater. 132 (2006), 220–225
  17. A. Renzoni, F. Zino, E. Franchi, Environ. Res. A 77 (1998) 68–72.
  18. J.M. Benoit, W.F. Fitzgerald, A.W.H. Damman, Environ. Res. A 78 (1998) 118–133.
  19. J. H. Wanga, Y. M. Liub, Z. M. Donga, J. B. Chaob, H. Wang, Y. Wanga, Journal of Hazardous Materials 382 (2020) 121056
  20. S. Das, H. K. Indurthi, P. Asati, P. Saha, D. K. Sharma, Dyes and Pigments 199 (2022) 110074.
  21. G. Dhaka, J. Singh, N. Kaur, Inorganica Chimica Acta 462 (2017), 152–157.
  22. R. Hussain, M. Ashraf, S. Khan, F. Rahim, W. Rehman, M. Taha, A. Sardar, Y. Khan, I. Khan, S.A.A. Shah, J. Mol. Struct. 1295 (2024) 136582.
  23. A. Sardar, O-ur-R. Abid, S. Daud, B.A. Shah, W. Shahid, M. Ashraf, M. Fatima, S. Ezzine, A.Shareef A.Wadood, H.A. Al-Ghulikah, S.A. Alissa, Arab. J. Chem. 15 (2022) 104300.
  24. A.K. Jain, S. Sharma, A. Vaidya, V. Ravichandran, R.K. Agrawal, Chem. Biol. Drug Des. 81 (2013) 557–576.
  25. Md. Mohasin, Z. Alam, S. Ahmad,U. Salma, Q. Ullah, S. A. Khan, J.Mol.Struc.,1336 (2025), 142034.
  26. G.C. Santos, Y.G. Kappenberg, J.M. Rosa, A. Ketzer, M.A. Martins, G. Banacorsa, J. Photochem. Photobiol., A 444, (2023), 114900.
  27. T. Jabeen S. Aslam M. Yaseen, M.J. Saif, M. Ahmad, S.A. Al-Hussain M.E.A. Zaki, J. Saudi Chem. Soc. 27 (2023) 101679.
  28. Y. Khan, S. Khan, R. Hussain, A. Maalik, W. Rehman, M.W. Attwa, R. Masood, H. W. Darwish, H.A. Ghabbour, Pharmaceuticals, (Basel) 16 (2023) 1650.
  29. A. Khamitova, D. Berillo, A. Lozynskyi, Y. Konechnyi, D. Mural, V. Georgiyants, R. Lesyk, Mini. Rev. Med. Chem. 24 (2024).
  30. Md. Mohasin, Z. Alam, S. Ahmad,U. Salma, Q. Ullah, S. A. Khan, J.Mol.Struc.,1336 (2025), 142034.