Journals / Turkish Journal of Chemistry / 2013 / Cilt: 37 - Sayı: 3

Electrochemistry of 2,6-diaminopurine on multiwall carbon nanotube modified glassy carbon electrode

Pages
325–334
Publication Date
2013-03-01
DOI
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The electrocatalytic oxidation of 2,6-DAP on MWCNT/GCE showed that acid pretreated multiwall carbon nanotube can be used in new applications in electrochemical determinations of biologically important compounds.

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Objective & Hypothesis:The electrochemical oxidation of 2,6-diaminopurine (2,6-DAP) was studied in pH 7.4 phosphate buffer solution on multiwall carbon nanotube modified glassy carbon electrode (MWCNT/GCE) over a temperature range of 20 to 50 °C using cyclic voltammetry. 2,6-DAP oxidation on MWCNT/GCE showed a well-defined and irreversible oxidation peak at about 0.72 V vs.
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Key Findings & Data:The oxidation potential of 2,6-DAP linearly varied with pH over the range of 3.0 to 10.0 with a slope of --0.0547 V/pH, implying that 2 protons were accompanied by 2 electrons transferred in the electrochemical reaction.
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Conclusion & Impact:The electrocatalytic oxidation of 2,6-DAP on MWCNT/GCE showed that acid pretreated multiwall carbon nanotube can be used in new applications in electrochemical determinations of biologically important compounds.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Carbon nanotubes · 6-diaminopurine · activation energy

Abstract

The electrochemical oxidation of 2,6-diaminopurine (2,6-DAP) was studied in pH 7.4 phosphate buffer solution on multiwall carbon nanotube modified glassy carbon electrode (MWCNT/GCE) over a temperature range of 20 to 50 °C using cyclic voltammetry. 2,6-DAP oxidation on MWCNT/GCE showed a well-defined and irreversible oxidation peak at about 0.72 V vs. Ag/AgCl at pH 7.4. The oxidation potential of 2,6-DAP linearly varied with pH over the range of 3.0 to 10.0 with a slope of --0.0547 V/pH, implying that 2 protons were accompanied by 2 electrons transferred in the electrochemical reaction. The activation energy, Ea, of oxidation reaction was found to be 33.10 \pm 1.88 kJ/mol. The differential pulse voltammetric determination of 2,6-DAP was also studied. The peak currents increased linearly with increasing of the 2,6-DAP concentration range from 0.4 m mol/L to 80 m mol/L. The linear regression equation appeared as Ip/mA = --(1.66 \pm 0.42) + (4.21 \pm 0.11) [2,6-DAP]/m mol/L, R2 = 0.9982, and the detection limit (S/N = 3) was 3 \times 10-7 \pm 0.015 mol/L (n =3). The electrocatalytic oxidation of 2,6-DAP on MWCNT/GCE showed that acid pretreated multiwall carbon nanotube can be used in new applications in electrochemical determinations of biologically important compounds.

Özet

The electrochemical oxidation of 2,6-diaminopurine (2,6-DAP) was studied in pH 7.4 phosphate buffer solution on multiwall carbon nanotube modified glassy carbon electrode (MWCNT/GCE) over a temperature range of 20 to 50 °C using cyclic voltammetry. 2,6-DAP oxidation on MWCNT/GCE showed a well-defined and irreversible oxidation peak at about 0.72 V vs. Ag/AgCl at pH 7.4. The oxidation potential of 2,6-DAP linearly varied with pH over the range of 3.0 to 10.0 with a slope of --0.0547 V/pH, implying that 2 protons were accompanied by 2 electrons transferred in the electrochemical reaction. The activation energy, Ea, of oxidation reaction was found to be 33.10 \pm 1.88 kJ/mol. The differential pulse voltammetric determination of 2,6-DAP was also studied. The peak currents increased linearly with increasing of the 2,6-DAP concentration range from 0.4 m mol/L to 80 m mol/L. The linear regression equation appeared as Ip/mA = --(1.66 \pm 0.42) + (4.21 \pm 0.11) [2,6-DAP]/m mol/L, R2 = 0.9982, and the detection limit (S/N = 3) was 3 \times 10-7 \pm 0.015 mol/L (n =3). The electrocatalytic oxidation of 2,6-DAP on MWCNT/GCE showed that acid pretreated multiwall carbon nanotube can be used in new applications in electrochemical determinations of biologically important compounds.

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Cite This Article

AYAN, E. M., KARABİBEROĞLU, Ş. U., DURSUN, Z. (2013). Electrochemistry of 2,6-diaminopurine on multiwall carbon nanotube modified glassy carbon electrode. Turkish Journal of Chemistry, Cilt: 37 - Sayı: 3, 325–334. https://ajindex.com/articles/184851

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References (28)

  1. Diculescu, V. C.; Piedade, J. A. P.; Maria, A.; Brett, O. Bioelectrochem. 2007, 70, 141–146.
  2. Goyal, R. N.; Gupta, V. K.; Oyama, M.; Bachheti, N. Talanta 2007, 71, 1110–1117.
  3. Simoni, R. E.; Gomes, L. N. L. F.; Scalco, F. B.; Oliveira, C. P. H.; Neto, F. R. A.; Oliveria, M. L. C. J. Inherit. Metab. Dis. 2007, 30, 295–309.
  4. Nayan, R.; Dey, A. K. Z. Naturforsch. 1972, 27, 688–690.
  5. Yan, X.; Li, H.; Xu, Z.; Li, W. Bioelectrochem. 2009, 74, 310–314.
  6. Xie, X.; Yang, K.; Sun, D. Colloid. Surface. B 2008, 67, 261–264.
  7. Amri, C. E.; Maurel, M. C.; Baronc, M. H. Spectrochim. Acta Part A 2005, 61, 2049–2056.
  8. Amri, C. E.; Baronc, M. H.; Maurel M. C. Spectrochim. Acta Part A 2003, 59, 2645–2654.
  9. Gill, B. D.; Indyk, H. E. Int. Dairy J. 2007, 17, 596–605.
  10. Ganzera, M.; Vrabl, P.; Worle, E.; Burgstaller, W.; Stuppner, H. Anal. Biochem. 2006, 359, 132–140.
  11. Yeh, C. F.; Jiang, S. J. Analyst 2002, 127, 1324–1327.
  12. Liu, H.; Wang, G.; Chen, D.; Zhang, W.; Li, C.; Fang, B. Actuat. B Chem. 2008, 128, 414–421.
  13. Zen, J. M.; Chang, M. R.; Ilangovan, G. Analyst 1999, 124, 679–684.
  14. Zhang, R.; Wang X.; Chen, C. Electroanal. 2007, 19, 1623–1627. L¨ u, S. Microchem. J. 2004, 77, 37–42.
  15. Abdullin, T. I.; Nikitina, I. I.; Bondar, O. V. Russ. J. Electrochem. 2008, 44, 1444–1448.
  16. Wang, J.; Kawde, A. N.; Musameh, M. Analyst 2003, 128, 912–916.
  17. Lu, B. Y.; Li, H.; Deng, H.; Xu, Z.; Li, W. S.; Chen, H. Y. J. Electroanal. Chem. 2008, 621, 97–102.
  18. Jelen, F.; Kourilova, A.; Pecinka, P.; Palecek, E. Bioelectrochem. 2004, 63, 249–252.
  19. Trnkova, L.; Friml, J.; Dracka, O. Bioelectrochem. 2001, 54, 131–136.
  20. Szurley, E.; Toth, A. B. Anal. Chim. Acta 1983, 154, 323–327.
  21. Astwood, D.; Lippincott, T.; Deysher, M.; D’Amico, C.; Szurley, E.; Toth, A. B. J. Electroanal. Chem. 1983, 159, 295–312.
  22. Yao, T.; Musha, S. Bull. Chem. Soc. Japan 1979, 52, 2307–2311. Mavio˘ glu, E. Determination of the Thermodynamic Stability Constants and Thermodynamic Parameters of Metal Complexes of Some Purines, MSc Thesis, Ege University, 2001.
  23. Aladag, N.; Trnkova, L.; Kourilova, A.; Ozsoz, M.; Jelen, F. Electroanal. 2010, 22, 1675–1681. Ag¨ ui, L.; Sedeno, P. Y.; Pingarron, J. M. Anal. Chim. Acta 2008, 622, 11–47.
  24. Liu, G.; Riechers, S. L.; Mellen, M. C.; Lin, Y. Electrochem. Comm. 2005, 7, 1163–1169.
  25. Wang, Y. R.; Hu, P.; Liang, Q. L.; Luo, G. A.; Wang, Y. M. Chin. J. Anal. Chem. 2008, 36, 1011–1016.
  26. Trojanowicz, M. Trend. Anal. Chem. 2006, 25, 480–489.
  27. Jo, S.; Jeong, H.; Bae, S. R.; Jeon, S. Microchem. J. 2008, 88, 1–6.
  28. Wang, H. S.; Li, T. H