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Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives

Year 2008, Volume: 36 Issue: 4, 319 - 328, 01.12.2008
https://izlik.org/JA42WR27KB

Abstract

In this study we offer a new method to synthesize positively charged poly 1-Azabicyclo[4.2.0]octane -common nameis polyconidine- and its water-soluble polyampholyte derivative synthesized with bromoacetic acid using microwaveirradiation as a model carrier system for biological macromolecules like peptides, proteins and etc 1-Azabicyclo[4.2.0]octane containing unsubstituted four-membered azetidine ring was synthesized using microwaveassisted synthesis method and used as monomer in cationic ring-opening polymerization. Different alkyl halide derivatives were used as initiators to start polymerization. Microwave-assisted synthesis of polyconidine derivatives was carried out by bromoacetic acid using microwave irradiation. Characterization of polyconidine and its derivatives was achieved by size-exclusion chromatography SEC with on line quadruple detection system, ATR FT-IR and UV Spectroscopy

References

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  • 2. Schulz, R.C., Schmidt, M., Schwarzenbach, E., Zöller, J., Some new polyelectrolytes, Macromol. Chem., Macromol. Symp. 26, 221- 231, 1989.
  • 3. Zaikov, G.E., Livshits V.S., Biodegradable polymers for medical purposes, Khim.-farm. Zh., No. 4, 416-427, 1984.
  • 4. Penczek, S., Cypryk, M., Duda, A., Kubisa, P., Slomkawski, S., Living ring-opening polymerizations of heterocyclic monomers, Prog. Polym. Sci. 32, 247, 2007.
  • 5. Mühlbach, K., Schulz, R.C., Polymers of 1- Azabicyclooctane[4.2.0]. Part 3. Modification of polystyrene-block-poly-1- azabicyclooctane[4.2.0], Acta Polymer. 46, 130-133, 1995.
  • 6. Nekrasov, A. V., Berestetskaya, T. Z., Kinetics and mechanism of copolymerization of conidine and β-propiolactone, Polymer Science U.S.S.R. 26, 1165, 1984.
  • 7. Mühlbach, K., Schulz, R.C., Polymers of 1- azabicyclo[4.2.0]octane, 1, Structure of monomer and homopolymer, Makromol. Chem. 189, 1267, 1988.
  • 8. Matyjaszewski, K., Cationic polymerization of 1-azabicyclo[4.2.0]octane 1, Alkylation, Makromol. Chem. 185, 37-49, 1984.
  • 9. Kropachev, V. A., Polymerization of heterocycles related to biomedical polymers, Pure and Applied Chem., 48, 355-361, 1976.
  • 10. Matyjaszewski, K., Szymanski, R., Kubisa, P., Penczek, ST., Ionic and covalent species in the cationic polymerization- equilibria and reactivities, Acta Polymer. 35, Nr. 1, 14, 1984.
  • 11. Topuzoğulları, M., Çimen, N.S., Mustafaeva, Z., Mustafaev, M., Molecular-weight distribution and structural transformation in water-soluble complexes of poly(acrylic acid) and bovine serum albumine, Eur. Poly. Jour., 43, 2935- 2946, 2007.
  • 12. Matyjaszewski, K. (Ed), Cationic Polymerizations: mechanisms, synthesis and applications, Marcel Dekker, Inc., 1996.
  • 13. Mustafaev M.I., Mustafaeva Z., Bermek E., Osada Y., New amphiphilic immunogens by Cu2+-mediated complexes of water-born poly(N-isopropylacrylamide) and bovine serum albumin, J. Bioact. Compat. Polymers 13, 33- 49, 1998.

Year 2008, Volume: 36 Issue: 4, 319 - 328, 01.12.2008
https://izlik.org/JA42WR27KB

Abstract

References

  • 1. Lavagnino, E. R., Chauvette, R. R., Cannon, W. N., Kornfield, E. C., Conidine-synthesis, polymerization and derivatives, J. Amer. Chem. Soc. 82, 2609, 1960.
  • 2. Schulz, R.C., Schmidt, M., Schwarzenbach, E., Zöller, J., Some new polyelectrolytes, Macromol. Chem., Macromol. Symp. 26, 221- 231, 1989.
  • 3. Zaikov, G.E., Livshits V.S., Biodegradable polymers for medical purposes, Khim.-farm. Zh., No. 4, 416-427, 1984.
  • 4. Penczek, S., Cypryk, M., Duda, A., Kubisa, P., Slomkawski, S., Living ring-opening polymerizations of heterocyclic monomers, Prog. Polym. Sci. 32, 247, 2007.
  • 5. Mühlbach, K., Schulz, R.C., Polymers of 1- Azabicyclooctane[4.2.0]. Part 3. Modification of polystyrene-block-poly-1- azabicyclooctane[4.2.0], Acta Polymer. 46, 130-133, 1995.
  • 6. Nekrasov, A. V., Berestetskaya, T. Z., Kinetics and mechanism of copolymerization of conidine and β-propiolactone, Polymer Science U.S.S.R. 26, 1165, 1984.
  • 7. Mühlbach, K., Schulz, R.C., Polymers of 1- azabicyclo[4.2.0]octane, 1, Structure of monomer and homopolymer, Makromol. Chem. 189, 1267, 1988.
  • 8. Matyjaszewski, K., Cationic polymerization of 1-azabicyclo[4.2.0]octane 1, Alkylation, Makromol. Chem. 185, 37-49, 1984.
  • 9. Kropachev, V. A., Polymerization of heterocycles related to biomedical polymers, Pure and Applied Chem., 48, 355-361, 1976.
  • 10. Matyjaszewski, K., Szymanski, R., Kubisa, P., Penczek, ST., Ionic and covalent species in the cationic polymerization- equilibria and reactivities, Acta Polymer. 35, Nr. 1, 14, 1984.
  • 11. Topuzoğulları, M., Çimen, N.S., Mustafaeva, Z., Mustafaev, M., Molecular-weight distribution and structural transformation in water-soluble complexes of poly(acrylic acid) and bovine serum albumine, Eur. Poly. Jour., 43, 2935- 2946, 2007.
  • 12. Matyjaszewski, K. (Ed), Cationic Polymerizations: mechanisms, synthesis and applications, Marcel Dekker, Inc., 1996.
  • 13. Mustafaev M.I., Mustafaeva Z., Bermek E., Osada Y., New amphiphilic immunogens by Cu2+-mediated complexes of water-born poly(N-isopropylacrylamide) and bovine serum albumin, J. Bioact. Compat. Polymers 13, 33- 49, 1998.
There are 13 citations in total.

Details

Primary Language English
Authors

Erdem Karabulut This is me

Zafer Ömer Özdemir

Çiğdem Yolaçan This is me

Yunus Sarıçay This is me

Zeynep Mustafaeva This is me

Publication Date December 1, 2008
IZ https://izlik.org/JA42WR27KB
Published in Issue Year 2008 Volume: 36 Issue: 4

Cite

APA Karabulut, E., Özdemir, Z. Ö., Yolaçan, Ç., Sarıçay, Y., & Mustafaeva, Z. (2008). Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives. Hacettepe Journal of Biology and Chemistry, 36(4), 319-328. https://izlik.org/JA42WR27KB
AMA 1.Karabulut E, Özdemir ZÖ, Yolaçan Ç, Sarıçay Y, Mustafaeva Z. Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives. HJBC. 2008;36(4):319-328. https://izlik.org/JA42WR27KB
Chicago Karabulut, Erdem, Zafer Ömer Özdemir, Çiğdem Yolaçan, Yunus Sarıçay, and Zeynep Mustafaeva. 2008. “Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives”. Hacettepe Journal of Biology and Chemistry 36 (4): 319-28. https://izlik.org/JA42WR27KB.
EndNote Karabulut E, Özdemir ZÖ, Yolaçan Ç, Sarıçay Y, Mustafaeva Z (December 1, 2008) Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives. Hacettepe Journal of Biology and Chemistry 36 4 319–328.
IEEE [1]E. Karabulut, Z. Ö. Özdemir, Ç. Yolaçan, Y. Sarıçay, and Z. Mustafaeva, “Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives”, HJBC, vol. 36, no. 4, pp. 319–328, Dec. 2008, [Online]. Available: https://izlik.org/JA42WR27KB
ISNAD Karabulut, Erdem - Özdemir, Zafer Ömer - Yolaçan, Çiğdem - Sarıçay, Yunus - Mustafaeva, Zeynep. “Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives”. Hacettepe Journal of Biology and Chemistry 36/4 (December 1, 2008): 319-328. https://izlik.org/JA42WR27KB.
JAMA 1.Karabulut E, Özdemir ZÖ, Yolaçan Ç, Sarıçay Y, Mustafaeva Z. Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives. HJBC. 2008;36:319–328.
MLA Karabulut, Erdem, et al. “Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives”. Hacettepe Journal of Biology and Chemistry, vol. 36, no. 4, Dec. 2008, pp. 319-28, https://izlik.org/JA42WR27KB.
Vancouver 1.Karabulut E, Özdemir ZÖ, Yolaçan Ç, Sarıçay Y, Mustafaeva Z. Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives. HJBC [Internet]. 2008 Dec. 1;36(4):319-28. Available from: https://izlik.org/JA42WR27KB

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