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

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.

___

  • 1. Katon JE, editor. Organic Semiconducting Polymers. Marcel Dekker: New York, NY, USA, 1968.
  • 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. 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. Ragimov AV, Mamedov BA, Yasamova SY. New efficient dielectric and antistatic materials based on oligoaminophenols. Polymer 1997;43:343-347.
  • 5. Kaliyappan T, Kannan P. Co-ordination polymers. Prog. Polymer Sci. 2000;25:343-370.
  • 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. 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. 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.
  • 9. Grigoras M, Catanescu CO. Imine oligomers and polymers. J. Macromol. Sci-Pol R 2004;C44:131-173.
  • 10. Ayyagari MS, Marx KA, Tripathy SK, Akara JA, Kaplan DL. Controlled free-radical polymerization of phenol derivatives by enzyme-catalyzed reactions in organic solvents. Macromolecules 1995;28:5192-5197.
  • 11. Kaya İ, Gökpınar M, Kamacı M. Reaction Conditions, Photophysical, Electrochemical, Conductivity, and Thermal Properties of Polyazomethines. Macromol. Res. 2017;25:739-748.