Macromolecular Research

  • 제14권3호
  • /
  • Pages.255-256
  • /
  • 2006
  • /
  • 1598-5032(pISSN)
  • /
  • 2092-7673(eISSN)
한국고분자학회 (The Polymer Society of Korea)
권호 표지

Preparation of a Reactive Poly(phenylenemethylene) and Its Application for an Amphiphilic Architecture

  • Shin Dong-Mi (Division of Material Engineering, Graduate School of Natural Science & Technology Kanazawa University) ;
  • Ozeki Natsuki (Division of Material Engineering, Graduate School of Natural Science & Technology Kanazawa University) ;
  • Nakamoto Yoshiaki (Division of Material Engineering, Graduate School of Natural Science & Technology Kanazawa University) ;
  • Konishi Gen-Ichi (Division of Material Engineering, Graduate School of Natural Science & Technology Kanazawa University)
  • 발행 : 2006.06.01
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초록

키워드

참고문헌

  1. A. Knop and L. A. Plato, Phenolic Resins, Springer-Velag, Berlin, 1985
  2. Y.-J. Kim, H. Uyama, and S. Kobayashi, Polym. J., 36, 992 (2004) https://doi.org/10.1295/polymj.36.992
  3. M. H. Choi and I. J. Chung, J. Appl. Polym. Sci., 90, 2316 (2004) https://doi.org/10.1002/app.12763
  4. S. Habaue, T. Seko, M. Isonaga, H. Ajiro, and Y. Okamoto, Polym. J., 35, 213 (2003) https://doi.org/10.1295/polymj.35.213
  5. G. Konishi, T. Kimura, T. Yamagishi, and Y. Nakamoto, J. Network Polym. Jpn., 25, 200 (2004)
  6. D. Shin and G. Konishi, et al., Manuscript in preparation
  7. R. Charvet, D.-L. Jiang, and T. Aida, Chem. Commun., 23, 2664 (2004)
  8. T. K. Kyoung, H. L. Im, C. Park, Y. Song, and C. Kim, Macromol. Res., 12, 528 (2004) https://doi.org/10.1007/BF03218438
  9. K. Ishizu, Polym. J., 36, 775 (2004) https://doi.org/10.1295/polymj.36.775
  10. C.-S. Cho, I.-K. Park, J.-W. Nah, and T. Akaike, Macromol. Res., 11, 2 (2003) https://doi.org/10.1007/BF03218270
  11. K. Naka, H. Itoh, S.-Y. Park, and Y. Chujo, Polym. Bull., 52, 171 (2004)
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  13. Selected spectral data of 3: $^1H$ NMR (270 MHz; $CDCl_3$, TMS) $\delta$ 1.82-2.12 (Ar-C$H_3$), 3.42-3.64 (-OC$H_3$ & -C$H_2$Br), 3.81-3.95 (Ar-C$H_2$-Ar), 4.16-4.21 (-OC$H_2$-C$H_2$-)
  14. Selected spectral data of 4: $^1H$ NMR (270 MHz; $CDCl_3$, TMS) $\delta$ 1.95-2.28 (Ar-C$H_3$), 2.02-2.23(C$H_3$-C=O), 3.21-3.92 (-OC$H_3$ & -C$H_2$& Ar-C$H_2$-Ar & C$H_2$-NC=O), FT-IR (KBr) 3400(N-H), 2940(-C$H_2$-), 2850(OC$H_3$), 1620 (C=O), 1420 (Ar C=C), 1260 (Ph-O-C) $cm^{-1}$
  15. S. Kobayashi, M. Kaku, and T. Saegusa, Macromolecules, 21, 334 (1988) https://doi.org/10.1021/ma00180a009