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Photocure Reactions of Photoreactive Prepolymers with Cinnamate Groups

  • Kim, Whan-Gun (Department of Chemical and Biological Engineering, Seokyeong University)
  • Received : 2010.10.19
  • Accepted : 2010.12.22
  • Published : 2011.03.20

Abstract

The photoreactive prepolymers with multifunctional cinnamate and bisphenol Atype cinnamate groups that could perform photodimerization without photoinitiators were synthesized by the reaction of t-cinnamic acids (CAs) and epoxy resins. Their photocure reaction rates and the extent of reaction conversion were measured with Fourier transform infrared spectroscopy, and these increased with the intensity of UVirradiation. The experimental data of these reaction rates showed the characteristics of nth-order kinetics reaction, and all kinetic constants of each photoreactive polymer with this equation were summarized. Although the GTR-1800-HCA and KWG1-EP-HCA with hydroxyl group substituted cinnamate showed lower reaction conversion rates and rate constant than GTR-1800-CA and KWG1-EP-CAwith an unsubstituted cinnamate group, GTR-1800-MCAand KWG1-EP-MCAwith methoxy group substituted cinnamate showed similar and higher reaction conversion rates than the former, respectively. These results were explained in terms of segmental mobility for photopolymerization by molecular interactions.

Keywords

References

  1. Yoon, H. G.; Kim,W. G. Polymer for Electronics; Munundang: Seoul, Korea, 2001.
  2. Koo, H. S.; Chen, M.; Pan, P. C. Thin Solid Films 2006, 515, 896. https://doi.org/10.1016/j.tsf.2006.07.159
  3. Sabnis, R. W. Display 1999, 20, 119. https://doi.org/10.1016/S0141-9382(99)00013-X
  4. Kudo, T.; Nanjo, Y.; Nozaki, Y.; Yamaguchi, H.; Kang,W.; Pawlowski,G. Japan J. Appl. Phys. 1998, 37, 1010. https://doi.org/10.1143/JJAP.37.1010
  5. Kim, W. G.; Lee, J. Y. J. Appl. Polym. Sci. 2004, 92, 43. https://doi.org/10.1002/app.13635
  6. Kim, W. G. J. Appl. Polym. Sci. 2008, 107, 3615. https://doi.org/10.1002/app.27436
  7. Seo, D. K.; Lim, H. S.; Lee, J. Y.; Kim, W. G. Mol. Cryst. Liq.Cryst. 2006, 445, 323.
  8. Lim,H. S.; Seo, D. K.; Lee, J.Y.;Kim,W. G.; Song, K. G. Mol. Cryst. Liq. Cryst. 2006, 445, 131.
  9. Tao, Z.; Yang, S.; Ge, Z.; Chen, J.; Fan, L. European. Polym. J.2007, 43, 550. https://doi.org/10.1016/j.eurpolymj.2006.10.030
  10. Decker, C. Macromol. Rapid Commun. 2002, 23, 1067. https://doi.org/10.1002/marc.200290014
  11. Egerton, P. L.; Pitts, E.; Reiser, A. Macromolecules 1981, 14, 95. https://doi.org/10.1021/ma50002a019
  12. Visconte, L. L. Y.; Andrade, C. T.; Azuma, C. J. Appl. Polym.Sci. 1998, 69, 907. https://doi.org/10.1002/(SICI)1097-4628(19980801)69:5<907::AID-APP9>3.0.CO;2-Q
  13. Kim, W. G.; Lee, J. Y. J. Appl. Polym. Sci. 2002, 86, 1942. https://doi.org/10.1002/app.11104
  14. Kim, W. G.; Lee, J. Y. Polymer 2002, 43, 5713. https://doi.org/10.1016/S0032-3861(02)00444-5
  15. Tazuke, S.; Hayashi, N. J. Polym. Sci.; Polym. Chem. Ed. 1978,16, 2729. https://doi.org/10.1002/pol.1978.170161101
  16. Tazuke, S.; Tanabe, T. Macromolecule 1979, 12, 853. https://doi.org/10.1021/ma60071a013
  17. Ninomiya, A.; Kawaguchi, H. Sci.& Tech. Adv.Mat. 2006, 7, 162. https://doi.org/10.1016/j.stam.2005.12.005

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