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[4+4] Cyclodimer of tert-Butyl 9-Anthroate and Furan and [4+4] Cyclodimers of Alkyl 9-Anthroate

  • Published : 1997.09.20

Abstract

Irradiation of tert-butyl 9-anthroate and furan through a Uranium glass filter gave the [4+4] cyclodimer (21.8%) of tert-butyl 9-anthroate and furan and the 1,4-10',9' cyclodimer (4.2%) of tert-butyl 9-anthroate as well as the 9,10-10',9' cyclodimer (65.7%) of tert-butyl 9-anthroate. The [4+4] cyclodimer of tert-butyl 9-anthroate and furan was found to be thermally dissociated into their unit components with the activation enthalpy of 35.6 kcal/mole and the activation entropy of 7.6 eu, and photochemically dissociated to produce excited tert-butyl 9-anthroate. Quantum yields for the photodissociation to tert-butyl 9-anthroate and the formation of excited tert-butyl 9-anthroate in cyclohexane at room temperature were determined to be 0.56 and 0.19, respectively. The 1,4-10',9' cyclodimer of tert-butyl 9-anthroate in DMF was thermally dissociated into tert-butyl 9-anthroate with the activation enthalpy of 34.8 kcal/mole and the activation entropy of 16.4 eu. Upon irradiation, the [4+4] cyclodimers of tert-butyl 9-anthroate and the [4+4] cyclodimers of methyl 9-anthroate were quantitatively dissociated. However, no adiabatic photoreversion was observed from any of the cyclodimers. Quantum yields for the photodissociation in cyclohexane at room temperature were measured and compared.

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References

  1. Chem. Rev. v.87 McCullough, J. J.
  2. J. Am. Chem. Soc. v.109 Yang, N. C.;Yang, X.
  3. Bull. Chem. Soc. Jpn. v.67 Kimura, M.;Okamoto, H.;Kashino, S.
  4. J. Am. Chem. Soc. v.104 Yang, N. C.;Chen, M.-J.;Chen. P.;Mak, K. T.
  5. J. Am. Chem. Soc. v.106 Yang, N. C.;Chen, M.-J.;Chen, P.
  6. J. Org. Chem. v.53 Kimura, M.;Okamoto, H.;Kura, H.;Okazaki, A.;Nagayasu, E.;Satake, K.;Morosawa, S.;Fukazawa, M.;Abdel-Halim, H.;Cowan, D. O.
  7. J. Chem. Soc., Perkin Trans. v.Ⅰ Kimura, M.;Kura, H.;Nukada, K.;Okamoto, H.;Satake, K.;Morosawa, S.Ⅰ
  8. Bull. Chem. Soc. Jpn. v.66 Okamoto, H.;Kimura, M.;Satake, K.;Morosawa, S.
  9. Tetrahedron Lett. v.52 Noh, T.;Kim, D.
  10. Bull. Korean Chem. Soc. v.18 Noh, T.;Kim, D.;Jang, S.
  11. J. Org. Chem. v.52 Albini, A.;Fasani, E.;Faiardi, D.
  12. J. Am. Chem. Soc. v.110 Albini, A.;Fasani, E.
  13. J. Am. Chem. Soc. v.110 Yang, N. C.;Noh, T.;Gan, H.;Halfon, S.;Hrnjez, B. J.
  14. Bull. Korean Chem. Soc. v.18 Noh, T.;Lim, H.;Kim, D.
  15. Chem. Lett. Noh, T.;Lim. H.
  16. J. Phys. Chem. v.79 Shon, R. S. -L.;Cowan, D. O.;Schmiegel, W. W.
  17. J. Phys. Chem. v.80 Werner, T. C.;Matthews, T.;Soller, B.
  18. Tetrahedron Lett. v.26 Felix, G.;Lapouyade, R.;Bouas-Laurent, H.;Clin, B.
  19. Chem. Phys. Lett. v.78 Ferguson, J.;Castellan, A.;Desvergne, J.-P.;Bouas-Laurent, H.
  20. J. Chem. Soc., Perkin Trans. Ⅱ Desvergne, J.-P.;Bitit, N.;Castellan, A.;Webb, M.;Bouas-Lauren, H.
  21. J. Chem. Soc. Chem. Commun. Fages, F.;Desvergne, J.-P.;Frisc, I.;Bouas-Laurent, H.;
  22. J. Photochem. Photobiol. A: Chem. v.97 Becker, H.-D.;Becker, H.-C.;Langer, V.
  23. Elements of Organic Photochemistry Cowan, D. O.;Drisko, R. L.
  24. Photochromism; Molecules and Systems Bouas-Laurent, H.;Desvergne, J.-P.;Durr, H.(Ed.);Bouas-Laurent, H.(Ed.)
  25. Helv. Chim. Acta. v.57 Belus, D.;Rist, G.
  26. J. Am. Chem. Soc. v.97 Kabakoff, D. S.;Bunzli, J.-C. G.;Oth, J. F. M.;Hammond, W. B.;Berson, J. A.
  27. Chem. Phys. Lett. v.88 Okada. T.;Kida, K.;Mataa, N.
  28. J. Am. Chem. Soc. v.105 Smothers, W. K.;Saltiel, J.
  29. Resonance in Organic chemistry Wheland, G. W.
  30. Angew. Chem. Int. Ed. Engl. v.18 Turro, N. J.;McVey, J.;Ramamurthy, V.;Lechtken, P.
  31. Photolumunescence of Solutions Parker, C. A.
  32. Handbook of Photochemistry Murov, S. L.