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Articles

Effect of reaction conditions on the homo and copolymerizations of N-(1-naphthyl)acrylamide

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Pages 276-284 | Received 06 Dec 2018, Accepted 07 Jan 2019, Published online: 08 Feb 2019

References

  • Yang, F., C. Li, J. Zhang, G. Feng, Z. Wei, and W. Li. 2016. Methylated conjugated polymers based on diketopyrrolopyrrole and dithienothiophene for high performance field-effect transistors. Org. Electron. 37:366–370.
  • Agneeswari, R., J. Lee, S. M. Park, S. Cho, Y. Jin, S. H. Park, and M. H. Hyun. 2016. Imide-linked alkyl chain influence on the properties of pyrrole-based imide-functionalized polymers containing pyrrolo[3,4-c]pyrrole-1,3(2H,5H)-dione and benzodithiophene units for polymer solar cells. Synthetic Met. 220:34–40.
  • Wen, Y., and J. Xu. 2017. Scientific importance of water-procesable PEDOT-PSS and preparation, challenge and new application in sensors of its film electrode: a review. J. Polym. Sci. Part A: Polym. Chem. 55:1121–1150.
  • Jo, J. W., J. H. Kim, and J. W. Jung. 2016. Isoindigo-based fluorinated low band gap polymers for environmentally stable field effect transistor. Dyes Pigments 133:333–338.
  • Kraft, U., K. Takimiya, M. J. Kang, R. Rodel, F. Letzks, J. N. Burghartz, E. Weber, and H. Klauk. 2016. Detailed analysis and contact properties of low-voltage organic thin-film transistors based on dinaphtho[2,3-b:2’,3’-f]thieno[3,2-b]thiophene (DNTT) and its didecyl and diphenyl derivatives. Org. Electron. 35:33–40.
  • Hoegel, H., and H. Schleisinger. (Murray Hill Co.) 1967. Electrophotographic Process Employing Photoconductive Polymers. U.S. Patent 3,307,940.
  • Diab, M. A., A. Z. El-Sonbati, A. A. El-Bindary, J. A. Hasanen, and S. M. Saad. 2014. Thermal stability and degradation of poly (N-(naphthalene-5-yl) Acrylamide) Homopolymer and copolymer of N-(naphthalene-5-yl) Acrylamide with methyl methacrylate. Topol. Supramol. Polym. Sci. 1:1–16.
  • Kaliyappan, T., S. Rajagopan, and P. Kannan. 2003. Studies on polyacrylates containing pendant ligand with carbonyl and hydroxyl functions and their divalent metal complexes. J. Appl. Polym. Sci. 90:2083–2090.
  • Mayo, F. R., and F. M. Lewis. 1944. Copolymerization. I. A basis for comparing the behavior of monomers in copolymerization; the copolymerization of styrene and methyl methacrylate. J. Am. Chem. Soc. 66:1594–1601.
  • Li, X. G., M. R. Huang, Z. L. Zhu, Y. Jin, and X. S. Wang. 2003. Structure and thermaldegradationofpoly(N‐phenylacrylamide) and poly(N‐phenylmethacrylamide). J. Appl. Polym. Sci. 88:1065–1071.
  • Oishi, T., and M. Fujimoto. 1982. Syntheses and polymerizationsofsomeN‐fluorenylacrylamide and methacrylamide. J. Polym. Sci. Part A. 20:2441–2455.
  • Negru, O. I., V. Barboiu, and M. Grigoras. 2011. Anthracene-based acrylamides and methacrylamides as functional monomers: synthesis and characterization. Acta Chem. IASI. 19:101–115.

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