화학공학소재연구정보센터
Macromolecular Research, Vol.10, No.4, 204-208, August, 2002
Imaging on a Vapor Deposited Film by Photopolymerization of a Rod-Like Molecule Consisting of Two Diacetylenic Groups
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A linear rod-like molecule, bis[4-(1,3-octadynyl)phenyl] terephthalate (2), consisting of two diacetylenic groups, was prepared. The unsymmetric diacetylene was prepared by the Cadiot-Chodkiewicz coupling reaction of 1-bromohexyne with 4-ethynylphenol and linked to a benzene core by an esterification reaction with terephthaloyl chloride in tetrahydrofuran. The thin film (200 nm thickness) of compound 2 was fabricated by the physical vapor deposition on a glass plate with a thermal evaporator. In the X-ray diffraction (XRD) study, the vapor deposited film on the glass plate showed peaks with d spacings of 19.4, 5.7, and 4.5 Å. This XRD pattern was quite different from that observed for compound 2 isolated by recrystallization from methylene chloride/hexane. The vapor deposited film was polymerized by UV irradiation. Photopolymerization was carried out through a photomask, resulting in a patterned image, where the irradiated part became isotropic.
  1. Trout TJ, Schmieg JJ, Gambogi WJ, Adv. Mater., 10, 1219 (1998) 
  2. Chang JY, Nam SW, Hong CG, Im JH, Kim JH, Han MJ, Adv. Mater., 13, 1298 (2001) 
  3. Nakagawa M, Oh SK, Ichimura K, Adv. Mater., 12, 403 (2000) 
  4. Theissen U, Zilker SJ, Pfeuffer T, Strohriegl P, Adv. Mater., 12, 1698 (2000) 
  5. Wegner G, Naturforsch., 24b, 824 (1969)
  6. Advances in Polymer Science, H.J. Cantow, Ed., Springer-Verlag, Berlin, vol. 63 (1984)
  7. Tieke B, Graf HJ, Wegner G, Naegele B, Ringsdorf H, Banerjie A, Day D, Lando JB, Colloid Polym. Sci., 255, 521 (1977) 
  8. Tieke B, Wegner G, Naegele B, Ringsdorf H, Angew. Chem., 88, 805 (1976)
  9. Kruchinin VN, Repinsky SM, Sveshnikova LL, Koshkina IM, Auvinen EM, Domnin IN, Thin Solid Films, 240(1-2), 131 (1994) 
  10. Batchelder DN, Evans SD, Freeman TL, Haussling L, Ringsdorf H, Wolf H, J. Am. Chem. Soc., 116(3), 1050 (1994) 
  11. Kim T, Crooks RM, Tetrahedron Lett., 35, 9501 (1994) 
  12. Peek BM, Callahan JH, Namboodiri K, Singh A, Gaber BP, Macromolecules, 27(1), 292 (1994) 
  13. Tsibouklis J, Adv. Mater., 7, 407 (1995) 
  14. Garito AF, Teng CC, Wong KY, Khamiri OZ, Mol. Cryst. Liq. Cryst., 106, 219 (1984)
  15. Hammond PT, Rubner MF, Macromolecules, 28(4), 795 (1995) 
  16. Chang JY, Baik JH, Lee CB, Han MJ, Hong SK, J. Am. Chem. Soc., 119(13), 3197 (1997) 
  17. Chang JY, Yeon JR, Shin YS, Han MJ, Hong SK, Chem. Mater., 12, 1076 (2000) 
  18. Brandsma L, Preparative Acetylenic Chemistry, 2nd Ed., Elsevier Science, New York (1988)
  19. Chang JY, Ji HJ, Han MJ, Bull. Korean Chem. Soc., 16, 674 (1995)
  20. Takahashi S, Kuroyama Y, Sonogashira K, Hagihara N, Synthesis, 627 (1980) 
  21. Austin WB, Bilow N, Kellaghan WJ, Lau KSY, J. Org. Chem., 46, 2280 (1981) 
  22. Barbu E, Tsibouklis J, Tetrahedron Lett., 37, 5023 (1996) 
  23. Mowery MD, Evans CE, Tetrahedron Lett., 38, 11 (1997) 
  24. Montierth JM, DeMario DR, Kurth MJ, Schore NE, Tetrahedron, 54, 11741 (1998)