TY - JOUR T1 - Microwave-Assisted Synthesis and Characterization of Poly 1-Azabicyclo[4.2.0]octane and Its Water-Soluble Derivatives AU - Karabulut, Erdem AU - Özdemir, Zafer Ömer AU - Yolaçan, Çiğdem AU - Sarıçay, Yunus AU - Mustafaeva, Zeynep PY - 2008 DA - December JF - Hacettepe Journal of Biology and Chemistry JO - HJBC PB - Hacettepe University WT - DergiPark SN - 2687-475X SP - 319 EP - 328 VL - 36 IS - 4 LA - en AB - 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 KW - Polyconidine KW - microwave-assisted polymer synthesis KW - cationic ring-opening polymerization CR - 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. CR - 2. Schulz, R.C., Schmidt, M., Schwarzenbach, E., Zöller, J., Some new polyelectrolytes, Macromol. Chem., Macromol. Symp. 26, 221- 231, 1989. CR - 3. Zaikov, G.E., Livshits V.S., Biodegradable polymers for medical purposes, Khim.-farm. Zh., No. 4, 416-427, 1984. CR - 4. Penczek, S., Cypryk, M., Duda, A., Kubisa, P., Slomkawski, S., Living ring-opening polymerizations of heterocyclic monomers, Prog. Polym. Sci. 32, 247, 2007. CR - 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. CR - 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. CR - 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. CR - 8. Matyjaszewski, K., Cationic polymerization of 1-azabicyclo[4.2.0]octane 1, Alkylation, Makromol. Chem. 185, 37-49, 1984. CR - 9. Kropachev, V. A., Polymerization of heterocycles related to biomedical polymers, Pure and Applied Chem., 48, 355-361, 1976. CR - 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. CR - 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. CR - 12. Matyjaszewski, K. (Ed), Cationic Polymerizations: mechanisms, synthesis and applications, Marcel Dekker, Inc., 1996. CR - 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. UR - https://dergipark.org.tr/en/pub/hjbc/issue//925939 L1 - https://dergipark.org.tr/en/download/article-file/1727560 ER -