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Year 2018, , 919 - 930, 01.01.2018
https://doi.org/10.18596/jotcsa.374150

Abstract

References

  • 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.

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

Year 2018, , 919 - 930, 01.01.2018
https://doi.org/10.18596/jotcsa.374150

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.

References

  • 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.
There are 11 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Articles
Authors

FEYZA Kolcu

Publication Date January 1, 2018
Submission Date January 3, 2018
Acceptance Date July 23, 2018
Published in Issue Year 2018

Cite

Vancouver Kolcu F. Synthesis, Characterization and Optimum Reaction Conditions of Oligo-N-Salicylidenephenylhydrazone via Oxidative Polymerization. JOTCSA. 2018;5(2):919-30.