Bulletin of the Korean Chemical Society

  • 제19권3호
  • /
  • Pages.299-307
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  • 1998
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Theroetical Study of the Nonlinear Optical Properties of Thiophene, Furan, Pyrrole, (1,2,4-triazole), (1,3,4-oxadiazole), and (1,3,4-thiadiazole) Monomers and Oligomers

  • 발행 : 1998.03.20
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초록

PM3 semiempirical calculations were carried out to study the frequency-dependent nonlinear optical properties of thiophene, furan, pyrrole, (1,2,4)-triazole, (1,3,4)-oxadiazole, and (1,3,4)-thiadiazole monomers and oligomers. The longitudinal component, αxx, is the largest of three principle components. On the other hand, the out-of-plane component, αzz, is the smallest. Moreover, the out-of-plane component (αzz) of thiophene, furan, pyrrole, (1,2,4)-triazole, (1,3,4)-oxadiazole, and (1,3,4)-thiadiazole monomers show constant changes with increasing optical frequencies. The frequency-dependent first- order polarizabilities increase in the order: thiophene > (1,2,4)-triazole > pyrrole > furan > (1,3,4)-thiadiazole > (1,3,4)-oxa-diazole monomers and oligomers. The effects of β(-2ω;ω,ω) (SHG) shows a larger dispersion compared with (-ω;ω,0) (EOPE) and β(0;-ω,ω) (OR). The second- order polarizabilities of thiophene, furan, pyrrole, (1,2,4)-triazole, (1,3,4)-thiadiazole, and (1,3,4)-oxadiazole monomers for the various second- order effects have the order: β(-2ω;ω,ω) (SHG) > β(-ω;ω,0) (EOPE) > β(0;-ω,ω) (OR) and thiophene > pyrrole > (1,2,4)-triazole > furan > 1,3,4-thiadiazole > 1,3,4-oxadiazole monomers. The third- order polarizabilities for the various third- order effects have the following order: γ(-3ω;ω',ω,ω) (THG) > γ(-2ω;0,ω,ω) (EFISHG) > γ(-ω;ω',-ω,ω) (IDRI) > γ(-ω;0,0,ω) (OKE). The effects of THG increase rapidly with increasing optical frequencies compared with the other effects. In particular, OKE effects increase most slowly with increasing optical frequencies. Also, the effects of THG for thiophene, furan, pyrrole, (1,2,4)-triazole, (1,3,4)-thiadiazole, and (1,3,4)-oxadiazole oligomers show the order thiophene > (1,2,4)-triazole > furan > pyrrole > (1,3,4)-thiadiazole > (1,3,4)-oxadiazole oligomers. In particular, the third- order polarizabilities of thiophene and (1,3,4)-thiadiazole oligomers are about four and three times larger than those of (1,3,4)-oxadiazole and (1,2,4)-triazole oligomer, respectively.

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참고문헌

  1. Adv. Polym. Sci. v.90 Billingham, N. C.;Calvert, P. D.
  2. Handbook of Conducting Polymers v.1;2 Skotheim, T. A.
  3. Chem. Mater. v.7 Pan, H.;Gao, X.;Zhang, Yue.;Prasad, P. N.
  4. J. Chem. Phys. v.60 Levenson, M. D.;Bloembergen, N.
  5. J. Chem. Phys. v.63 Levine, B. F.;Bethea, C. G.
  6. J. Chem. Phys. v.67 Oudar, J. L.
  7. Opt. Comm. v.25 Dulcic, A.;Flytzanis, C.
  8. J. Chem. Phys. v.74 Zyss, J.;Chemla, D. S.;Nicoud, J. F.
  9. J. Phys. Chem. v.99 Keshari, V.;Wijekoon, W. M. K. P.;Prasad, P. N.;Karna, P.
  10. J. Chem. Phys. v.95 Karna, S. P.;Talapatra, G. B.;Prasad, P. N.
  11. J. Phys. Chem. v.96 Li, D.;Marks, T. J.;Ratner, M. A.
  12. J. Comp. Chem. v.10 Stewart, J. J. P.
  13. J. Chem. Phys. v.104 Bishop, D. M.;De Kee, D. W.
  14. J. Chem. Phys. v.100 Bishop, D. M.
  15. J. Phys. Chem. v.99 Keshari, V.;Wijekoon, W. M. K. P.;Prasead, P. N.;Karna, P.
  16. Choi, U-.S.;
  17. Opt. Commun. v.10 Rustagi, K. C.;Ducuing, J.
  18. J. Chem. Phys. v.133 Barzoukas, M.;Blanchard-Desce, M.;Josse, D.;Lehn, J.-M;Zyss,
  19. J. Bull. Korean. Chem. Soc. v.15 Choi, U-. S.;Lee, W. R.;Kim, C.
  20. J. Chem. Phys. v.94 Karna, S. P.;Prasad, P. N.
  21. J. Chem. Phys., Faraday Trans. 2 v.85 Morly, J. O.;Pavlides, P.;Pugh, D.
  22. J. Chem. Phys. v.89 Hurst, G. J. B.;Dupuis, M.;Clementi, E.
  23. Chem. Phys. Lett. v.17 Daniel, C.;Dupuis, M.
  24. J. Chem. Phys. v.91 Pierce, B.
  25. Phys. Rev. B v.90 Shuai, Z.;Bredas, J. L.
  26. Phys. Rev. B v.46 Shuai, Z.;Bredas, J. L.
  27. Phys. Rev. Lett. v.68 Bosma, W. B.;Mukamel, S.;Greene, B. I.;Schmitt-Rink, S.
  28. Phys. Rev. B v.46 Shuai, Z.;Bredas, J. L.
  29. J. Am. Chem. Soc. v.115 Craig, G. S. W.;Cohen, R. E.;Schrock, R. R.;Silbey, R. J.;Pucetti, G.;Ledoux, I.;Zyss, J.
  30. Chem. Phys. Lett. v.140 de Molo, C. P.;Silbey, R.
  31. J. Chem. Phys. v.98 Beljonne, D.;Shuai, Z.;Bredas, J. L.
  32. J. Chem. Phys. v.89 Zhao, M.-T.;Singh, B. P.;Prasad, P. N.
  33. Phys. Rev. Lett. v.65 Thienpont, H.;Rikken, G. L. J. A.;Meijer, E. W.