Advertisement

Electrochemical synthesis, characterization, and spectroelectrochemical evaluation of poly(para amino benzoic acid-co-4,4-diaminodiphenyl sulfone) film

  • Fatemeh Ganjeizadeh Rohani
  • Alireza Mohadesi
  • Mehdi AnsariEmail author
Article
  • 40 Downloads

Abstract

A novel poly(para amino benzoic acid-co-4,4-diamino diphenyl sulfone), i.e., pABA-co-DDS, was synthesized by simple electro-polymerization processes. Its structural properties were characterized using Fourier transform infrared (FTIR) spectroscopy. The copolymer displayed different voltammetry behaviors by applying various DDS concentrations. Among all examined pABA:DDS ratios, the 1:1 ratio provided the most suitable copolymer film on the surface of the electrode. The solubility tests revealed that the copolymer is just soluble in warm dimethyl sulfoxide (DMSO). Its electroconductivity was obtained to be 9.02 × 10−2 S cm−1. In conclusion, the synthesized novel conductive copolymer is an environmentally friendly substance that can be used in many areas.

Abbreviations

pABA

Para-aminobenzoic acid

DDS

4,4-Diamino diphenyl sulfone

Notes

References

  1. 1.
    P.K. Ho, J.-S. Kim, J.H. Burroughes, H. Becker, S.F. Li, T.M. Brown, F. Cacialli, R.H. Friend, Nature 404, 481 (2000)CrossRefGoogle Scholar
  2. 2.
    S. Möller, C. Perlov, W. Jackson, C. Taussig, S.R. Forrest, Nature 426, 166 (2003)CrossRefGoogle Scholar
  3. 3.
    J.L. Boehme, D.S. Mudigonda, J.P. Ferraris, Chem. Mater. 13, 4469 (2001)CrossRefGoogle Scholar
  4. 4.
    A.A. Argun, P.-H. Aubert, B.C. Thompson, I. Schwendeman, C.L. Gaupp, J. Hwang, N.J. Pinto, D.B. Tanner, A.G. MacDiarmid, J.R. Reynolds, Chem. Mater. 16, 4401 (2004)CrossRefGoogle Scholar
  5. 5.
    G.D. Stucky, Nature 410, 885 (2001)CrossRefGoogle Scholar
  6. 6.
    Y. Liu, N. Song, Z. Ma, K. Zhou, Z. Gan, Y. Gao, S. Tang, C. Chen, MCP 223, 548 (2019)Google Scholar
  7. 7.
    X. Wang, W. Tan, Y. Wang, D. Wu, Y. Kong, Sens. Actuators B: Chem. 284, 63 (2019)CrossRefGoogle Scholar
  8. 8.
    X. Wang, W. Tan, H. Ji, F. Liu, D. Wu, J. Ma, Y. Kong, Sens. Actuators B: Chem. 264, 240 (2018)CrossRefGoogle Scholar
  9. 9.
    N.F. Atta, A. Galal, H.B. Mark, T. Yu, P.L. Bishop, Talanta 47, 987 (1998)CrossRefGoogle Scholar
  10. 10.
    J. Cha, J.I. Han, Y. Choi, D.S. Yoon, K.W. Oh, G. Lim, Biosens. Bioelectron. 18, 1241 (2003)CrossRefGoogle Scholar
  11. 11.
    W. Lu, H. Zhao, G.G. Wallace, Anal. Chim. Acta 315, 27 (1995)CrossRefGoogle Scholar
  12. 12.
    D.T. McQuade, A.E. Pullen, T.M. Swager, Chem. Rev. 100, 2537 (2000)CrossRefGoogle Scholar
  13. 13.
    T.A. Skotheim, J. Reynolds, B.C. Thompson Handbook of Conducting Polymers Fourth Edition – 2 Volume Set. CRC Press LLC, (2019)Google Scholar
  14. 14.
    X. Li, Y. Wan, C. Sun, J. Electroanal. Chem. 569, 79 (2004)CrossRefGoogle Scholar
  15. 15.
    G. Jin, Y. Zhang, W. Cheng, Sens. Actuators B: Chem. 107, 528 (2005)CrossRefGoogle Scholar
  16. 16.
    A. Benyoucef, F. Huerta, J. Vázquez, E. Morallon, Eur. Polym. J. 41, 843 (2005)CrossRefGoogle Scholar
  17. 17.
    C. Thiemann, C.M. Brett, SynMe 123, 1 (2001)Google Scholar
  18. 18.
    A. Gök, B. Sarı, M. Talu, SynMe 142, 41 (2004)Google Scholar
  19. 19.
    A. Dan, P. Sengupta, J. Appl. Polym. Sci. 90, 2337 (2003)CrossRefGoogle Scholar
  20. 20.
    P. Manisankar, A. Sarpudeen, S. Viswanathan, J. Pharm. Biomed. Anal. 26, 873 (2001)CrossRefGoogle Scholar
  21. 21.
    P. Manisankar, D. Ilangeswaran, Electrochim. Acta 55, 6546 (2010)CrossRefGoogle Scholar
  22. 22.
    D. Ilangeswaran, P. Manisankar, Electrochim. Acta 87, 895 (2013)CrossRefGoogle Scholar
  23. 23.
    Y.-H. Ho, A.P. Periasamy, S.-M. Chen, Sensors Actuators B: Chem. 156, 84 (2011)CrossRefGoogle Scholar
  24. 24.
    P. Manisankar, C. Vedhi, G. Selvanathan, H.G. Prabu, Electrochim. Acta 52, 831 (2006)CrossRefGoogle Scholar
  25. 25.
    S.L. Moura, J.R.d. Santos, F.B.C. Júnior, E.Y. Machado, L.F.d.A. Kawachi, Ferrão, J. Electroanal. Chem. 757, 230 (2015)CrossRefGoogle Scholar
  26. 26.
    Y. Kong, Y. Sha, S. Xue, Y. Wei, JElS 161, H249 (2014)Google Scholar
  27. 27.
    C. Chen, Z. Gan, C. Xu, L. Lu, Y. Liu, Y. Gao, Electrochim. Acta 252, 226 (2017)CrossRefGoogle Scholar
  28. 28.
    C. Chen, Z. Gan, K. Zhou, Z. Ma, Y. Liu, Y. Gao, Electrochim. Acta 283, 1649 (2018)CrossRefGoogle Scholar
  29. 29.
    X.G. Li, H.J. Zhou, M.R. Huang, M.F. Zhu, Y.M. Chen, J. Polym. Sci. Part A: Polym. Chem. 42, 3380 (2004)CrossRefGoogle Scholar
  30. 30.
    P. Manisankar, C. Vedhi, G. Selvanathan, R. Somasundaram, Chem. Mater. 17, 1722 (2005)CrossRefGoogle Scholar
  31. 31.
    C.-H. Yang, T.-C. Yang, C.-H. Chen, M.-S. Tsai, JElS 153, E85 (2006)Google Scholar
  32. 32.
    I. Gulaczyk, M. Kręglewski, A. Valentin, JMoSp 220, 132 (2003)Google Scholar
  33. 33.
    M. Rudolph, J. Electroanal. Chem. 529, 97 (2002)CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Pharmaceutics Research Center, Institute of NeuropharmacologyKerman University of Medical SciencesKermanIran
  2. 2.Plant Protection Research DepartmentKerman Agricultural and Natural Resources Research and Education Center, AREEOKermanIran
  3. 3.Department of ChemistryPayame Noor UniversityTehranIran

Personalised recommendations