Macromolecular Research

The Polymer Society of Korea (한국고분자학회)
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)
  • Published : 2006.06.01
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  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)
  12. K. Aoi, A. Takasu, M. Okada, and T. Imae, Macromol. Chem. Phys., 203, 2650 (2002) https://doi.org/10.1002/macp.200290040
  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