The synthesis and characterization of oligo-N-4-aminopyridine, oligo-2-[(pyridine-4-yl-imino) methyl] phenol and its some oligomer-metal complexes

Kaya İ., Koyuncu S.

POLYMER, vol.44, no.24, pp.7299-7309, 2003 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 44 Issue: 24
  • Publication Date: 2003
  • Doi Number: 10.1016/j.polymer.2003.09.011
  • Journal Name: POLYMER
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.7299-7309
  • Çanakkale Onsekiz Mart University Affiliated: Yes


The product and the oxidative polycondensation reaction conditions of oligo-4-aminopyridine were studied by using NaOCl as oxidant. Oligo-4-aminopyridine (4-OAP) was synthesized from the oxidative polycondensation of 4-aminopyridine (4-AP) in an aqueous solution medium acidic and neutral between 25 and 60 degreesC by using NaOCl as oxidant. About 85% of 4-AP was converted to 4-OAP. The number average molecular weight, (M-n) mass average molecular weight (M-w) and polydispersity index (PDI) values of 4-OAP synthesized were found to be 270, 850 g mol(-1) and 3.15, respectively, using NaOCl. The respective values of the Schiff base were 1721, 2256 g mol(-1) and 1.31, respectively, using air oxygen and 2173, 2372 g mol(-1) and 1.09, respectively, using NaOCl and 2749, 6432 g mol(-1) and 2.33, respectively, using H2O2. At the optimum reaction conditions, the yield of oligo-2-[(pyridine-4-yl-imino) methyl] phenol (OPMP) were found to be 86% (H2O2) and 89% (NaOCl) and 95% (air oxygen). The 4-OAP and OPMP were characterized by H-1 NMR, FT-IR, UV-Vis and elemental analysis. TG analysis showed to be stable of 4-OAP against thermo-oxidative decomposition. The weight loss of 4-OAP and its Schiff base oligomer was found to be 50, 86.39 and 71.78% at 525, 625 and 1000 degreesC, respectively. Also, new oligomeric Schiff base was synthesized from condensation of 4-AP with salicylaldehyde and their structures and properties were determined. During polycondensation reaction, a part of the azomethine (-CH=N-) groups oxidized to carboxylic (-COOH) group. Thus, soluble fraction in water of oligo-2[(pyridine-4-yl-imino) methyl] phenol involved in carboxylic (-COOH) (11%) group. Besides, the structure and properties of oligomermetal complexes of oligo-2-[(pyridine-4-yl-imino) methyl] phenol (OPMP) with Cu(II), Ni(II) and Co(II) were studied. Crown Copyright (C) 2003 Published by Elsevier Ltd. All rights reserved.