Research Article

Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization

Volume: 5 Number: 2 January 1, 2018
EN

Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization

Abstract

The oxidative polycondensation reaction conditions and optimum parameters of N-salicylidenephenylhydrazone (SPH) were determined using air, H2O2 and NaOCl as oxidants at a temperature range between 50 °C and 95 °C in an aqueous alkaline medium. The molecular structures of the obtained monomer and oligomer were confirmed by FT-IR, UV-Vis, 1H-NMR and elemental analyses. The characterization was fulfilled by TG-DTA, size exclusion chromatography (SEC) and solubility tests. The conversion of N-salicylidenephenylhydrazone into oligomer was performed using air, H2O2 and NaOCl as oxidants in an aqueous alkaline medium. According to SEC analysis, the number-average molecular weight (Mn), weight-average molecular weight (Mw) and polydispersity index (PDI) values of oligo-N-salicylidenephenylhydrazone (OSPH) obtained using NaOCl oxidant were found to be 1436 g mol-1, 1631 g mol-1 and 1.14, respectively. The conversion yield of N-salicylidenephenylhydrazone into oligo-N-salicylidenephenylhydrazone was 100% at optimum reaction conditions such as [SPH]0 = [KOH]0 = [H2O2]0 =0.06, mol/L and at 90 °C for 10 h. Also, according to TG-DTA analysis, oligo-N-salicylidenephenylhydrazone was shown to be thermally stable and resistant to thermo-oxidative decomposition. The weight loss of OSPH was found to be 20, 50 and 92.56% at 275°, 597° and 1000 °C, respectively.

Keywords

References

  1. 1. Katon JE, editor. Organic Semiconducting Polymers. Marcel Dekker: New York, NY, USA, 1968.
  2. 2. El-Shekeil AG, Al-Yusufy FA, Saknidy S. Synthesis and characterization of some soluble conducting polyazomethine polymers. Polym. Int. 1997;44:78-82.
  3. 3. Diaz FR, Moreno J, Tagle LH, East GA. Radic, D. Synthesis, characterization and electrical properties of polyimines derived from selenophene. Synthetic Met. 1999;100:187-193.
  4. 4. Ragimov AV, Mamedov BA, Yasamova SY. New efficient dielectric and antistatic materials based on oligoaminophenols. Polymer 1997;43:343-347.
  5. 5. Kaliyappan T, Kannan P. Co-ordination polymers. Prog. Polymer Sci. 2000;25:343-370.
  6. 6. Kaya İ, Demir HÖ, Vilayetoğlu AR. The synthesis and characterization of planar oligophenol with Schiff base substituent. Synthetic Met. 2002;126:183-191.
  7. 7. Kaya İ, Cihangiroğlu N. Synthesis, characterization and anti-microbial activity of oligo-N-2-aminopyridinylsalicylaldimine and some oligomer-metal complexes. J. Poly. Res. 2004;11:37-42.
  8. 8. Fakhari AR, Khorrami AR, Naeimi H. Synthesis and analytical application of a novel tetradentate N2O2 Schiff base as a chromogenic reagent for determination of nickel in some natural food samples. Talanta 2005;66:813-817.

Details

Primary Language

English

Subjects

Chemical Engineering

Journal Section

Research Article

Authors

Publication Date

January 1, 2018

Submission Date

January 3, 2018

Acceptance Date

July 23, 2018

Published in Issue

Year 2018 Volume: 5 Number: 2

APA
Kolcu, F. (2018). Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. Journal of the Turkish Chemical Society Section A: Chemistry, 5(2), 919-930. https://doi.org/10.18596/jotcsa.374150
AMA
1.Kolcu F. Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. JOTCSA. 2018;5(2):919-930. doi:10.18596/jotcsa.374150
Chicago
Kolcu, FEYZA. 2018. “Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization”. Journal of the Turkish Chemical Society Section A: Chemistry 5 (2): 919-30. https://doi.org/10.18596/jotcsa.374150.
EndNote
Kolcu F (January 1, 2018) Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. Journal of the Turkish Chemical Society Section A: Chemistry 5 2 919–930.
IEEE
[1]F. Kolcu, “Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization”, JOTCSA, vol. 5, no. 2, pp. 919–930, Jan. 2018, doi: 10.18596/jotcsa.374150.
ISNAD
Kolcu, FEYZA. “Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization”. Journal of the Turkish Chemical Society Section A: Chemistry 5/2 (January 1, 2018): 919-930. https://doi.org/10.18596/jotcsa.374150.
JAMA
1.Kolcu F. Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. JOTCSA. 2018;5:919–930.
MLA
Kolcu, FEYZA. “Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization”. Journal of the Turkish Chemical Society Section A: Chemistry, vol. 5, no. 2, Jan. 2018, pp. 919-30, doi:10.18596/jotcsa.374150.
Vancouver
1.FEYZA Kolcu. Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. JOTCSA. 2018 Jan. 1;5(2):919-30. doi:10.18596/jotcsa.374150

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