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Abstract:

The terpolymers containing oxadiazole pendant groups, obtained from chemical modification of a commercial polymer, present great interest due to their novelty and possible interesting properties. The synthesis of amidoxime-nitrile-3-hydroxyphenyl-1,2,4-oxadiazole (ANHOT) of different conversion times was prepared by chemical modification of polyacrylonitrile (PAN) as starting material. The first step of ANHOT synthesis was the well-known nitrile conversion into amidoxime groups. Afterwards, the 3,5-disubstituted 1,2,4-oxadiazolic ring was obtained by treatment of amidoxime-groups with an acyl chloride. The molecular structures were confirmed by IR, UV-Vis, 13C and 1H NMR spectroscopies. Conversion yields were calculated from elemental analysis. Thermal properties were studied by DSC and TGA techniques. All ANHOT series are completely soluble in very polar solvents. The dependency of viscosity with the conversion degree was analyzed with a control rate (CR) viscosimeter. Viscoelastic behavior was analyzed by rheometric measurements. The highest viscosity and elastic behavior were obtained with ANHOT of an hour conversion time; in this way it is the most attractive polymer among the ANHOT series. © 2006 Elsevier B.V. All rights reserved.

Registro:

Documento: Artículo
Título:PAN chemical modification: Synthesis and characterization of terpolymers with 1,2,4-oxadiazolic pendant groups
Autor:Vega, I.; Morris, W.; D'Accorso, N.
Filiación:Empresa de Servicios Especiales San Antonio Pride S.A., Carlos Pellegrini 1133, C1053ABW Buenos Aires, Argentina
Centro de Investigaciones en Hidratos de Carbono (CIHIDECAR-CONICET), Departamento de Química Orgánica, FCEyN, C1428EGA Buenos Aires, Argentina
Palabras clave:Amidoxime-nitrile-3-hydroxyphenyl-1,2,4-oxadiazole terpolymer; High viscosity; Polyacrylonitrile; Chemical modification; Molecular structure; Nuclear magnetic resonance spectroscopy; Polyacrylonitriles; Polymers; Synthesis (chemical); Viscosity; Amidoxime-nitrile-3-hydroxyphenyl-1,2,4-oxadiazole terpolymer; Control rate (CR); High viscosity; Rheometric measurements; Nitrogen compounds
Año:2006
Volumen:66
Número:12
Página de inicio:1609
Página de fin:1618
DOI: http://dx.doi.org/10.1016/j.reactfunctpolym.2006.06.004
Título revista:Reactive and Functional Polymers
Título revista abreviado:React Funct Polym
ISSN:13815148
CODEN:RFPOF
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13815148_v66_n12_p1609_Vega

Referencias:

  • Tu Chen, Y., Liu Ying, L., Lee Kueir, R., Lai Juin, Y., (2005) Polymer, 46, p. 6976
  • Herrero, M., Tiemblo, P., Reyes-Labarta, J., Mijangos, C., Reinecke, H., (2002) Polymer, 43, p. 2631
  • Chiou, S., Shine, J., (1989) J. Heterocycl. Chem., 26, p. 125
  • Gangloff, A., Litvak, J., Shelton, E., Sperandio, D., Wang, V., Rice, K., (2001) Tetrahedron Lett., 42, p. 1441
  • Rice, K., Nuss, J., (2001) Bioorg. Med. Chem. Lett., 26, p. 753
  • Huang, M., Li, X., Li, S., Zhang, W., (2004) React. Funct. Polym., 59, p. 53
  • Kizhnyaev, V., Gorkovenko, O., Safranov, A., Adamova, L., (1997) Vysokomol. Soed., 39, p. 527
  • Bronisz, R., (2004) Inorg. Chim. Acta, 357, p. 396
  • Annenkov, V., Kruglova, V., Alsarsur, I., Shvetsova, Zh., Aprelkova, N., Saraev, V., (2002) Vysokomol. Soed., 44, p. 2053
  • Saunders, J., Cassidy, M., Freedman, S., Harley, E., Iversen, L., Kneen, C., MacLeod, A., Baker, R., (1990) J. Med. Chem., 33, p. 1128
  • Swain, C., Baker, R., Kneen, C., Moseley, J., Saunders, J., Seward, E., Stevenson, G., Watring, K., (1991) J. Med. Chem., 34, p. 140
  • Torgova, S., Karamysheva, L., Strigazzi, A., (2002) Braz. J. Phys., 32, p. 593
  • Repke, D., Albrecht, H., Moffatt, J., (1975) J. Org. Chem., 40, p. 2481
  • Biçak, N., Atay, T., (1998) Turk. J. Chem., 22, p. 261
  • Ali, S., Wagner, D., Ayoub, J., Desroches, J., Morales, H., Price, P., Shepherd, D., White, S., (2002) Oilfield Rev., 14, p. 30. , and references therein
  • Oh, N., Jegal, J., Lee, K., (2001) J. Appl. Polym. Sci., 80, p. 1854

Citas:

---------- APA ----------
Vega, I., Morris, W. & D'Accorso, N. (2006) . PAN chemical modification: Synthesis and characterization of terpolymers with 1,2,4-oxadiazolic pendant groups. Reactive and Functional Polymers, 66(12), 1609-1618.
http://dx.doi.org/10.1016/j.reactfunctpolym.2006.06.004
---------- CHICAGO ----------
Vega, I., Morris, W., D'Accorso, N. "PAN chemical modification: Synthesis and characterization of terpolymers with 1,2,4-oxadiazolic pendant groups" . Reactive and Functional Polymers 66, no. 12 (2006) : 1609-1618.
http://dx.doi.org/10.1016/j.reactfunctpolym.2006.06.004
---------- MLA ----------
Vega, I., Morris, W., D'Accorso, N. "PAN chemical modification: Synthesis and characterization of terpolymers with 1,2,4-oxadiazolic pendant groups" . Reactive and Functional Polymers, vol. 66, no. 12, 2006, pp. 1609-1618.
http://dx.doi.org/10.1016/j.reactfunctpolym.2006.06.004
---------- VANCOUVER ----------
Vega, I., Morris, W., D'Accorso, N. PAN chemical modification: Synthesis and characterization of terpolymers with 1,2,4-oxadiazolic pendant groups. React Funct Polym. 2006;66(12):1609-1618.
http://dx.doi.org/10.1016/j.reactfunctpolym.2006.06.004