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Cyclopolymerization of 4,4-diphenoxy-1,6-heptadiyne by transition metal catalysts

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Summary

Cyclopolymerization was carried out by various catalyst systems. MoCl5-based catalyst systems are more effective for the polymerization of 4,4-diphenoxy-1,6-heptadiyne than WCl6-based catalyst systems. Polymerization of 4,4-diphenoxy-1,6-heptadiyne leads to soluble, purple colored polymer with number average molecular weight (Mn) of 3.6x104-5.2x104.1H- and13C-MNR, IR,and UV-visible spectra of the resulting polymer indicated that poly(4,4-diphenoxy-1,6-hepatadiyne) possesses a polyene structure presumably with cyclic recurring units in the polymer backbone. Poly(4,4-diphenoxy-1,6-heptadiyne) had good thermal and oxidative stability, and good solubility in organic solvents. The electrical conductivity of iodine-doped polymer was 10−3-10−2 S/cm.

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References

  1. For reviews, see: T. Masuda and T. Higashimura, Adv. Polym. Sci., 81, 121 (1986).

    Google Scholar 

  2. C. I. Simionescu and B. Percec, Prog. Polym. Sci. 8, 133 (1982).

    Google Scholar 

  3. T. Masuda, B. Z. Tang, T. Higashimura and H. Yamaoka, Macromolecules., 18,2369 (1985).

    Google Scholar 

  4. Y. H. Kim, Y. S. Gal, U. Y. Kim and S. K. Choi, Macromolecules., 21, 1991 (1988).

    Google Scholar 

  5. M. S. Chang, S. K. Kwon, and S. K. Choi, Macromolecules., 23, 4135 (1990).

    Google Scholar 

  6. M. S. Ryoo, W. C. Lee and S. K. Choi, Macromolecules. 23, 3029 (1990).

    Google Scholar 

  7. S. H. Han, U. Y. Kim, Y. S. Kang and S. K. Choi, Macromolecules., 24, 973 (1991).

    Google Scholar 

  8. Polymerization. A solution of MoCl5 (0.073 ml, 0.2 M chlorobenzene solution) is added to a solution of DPHD (0.2 g) and chlorobenzene (7.3 ml, [M]0=0.1) at room temperature. The polymerization was carried out at 60 °C for 24 h, and the polymerization was terminated by adding a small amount of methanol. The resulting polymer was precipitated with a large excess of diethyl ether. Polymer yield was determined by gravimetry.

  9. Y. H. Kim, K. Y. Choi and S. K. Choi, J. Polym. Sci. Polym. Lett. Ed., 27, 443 (1989).

    Google Scholar 

  10. O. K. Cho, Y. H. Kim, K. Y. Choi and S. K. Choi, Macromolecules., 23, 12 (1990).

    Google Scholar 

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Ahn, HK., Kim, YH., Jin, SH. et al. Cyclopolymerization of 4,4-diphenoxy-1,6-heptadiyne by transition metal catalysts. Polymer Bulletin 29, 625–632 (1992). https://doi.org/10.1007/BF01041147

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  • DOI: https://doi.org/10.1007/BF01041147

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