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EPR study of photoreduction of adducts of 3,6-di-tert-butyl-o-benzoquinone with dichlorocarbene

  • Physical Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    The formation of neutral and anion-radical particles was shown during the photoreduction of adducts of dichlorocarbene with 3,6-di-tert-butyl-o-benzoquinone in inert media and in the presence of amines, respectively.

  2. 2.

    The presence of thermo- and photoisomerization was shown for two forms of a neutral radical formed during the photoreduction of an adduct of 3,6-di-tert-butyl-o-benzoquinone with two dichlorocarbene fragments, consisting in opening of a three-membered ring with the formation of α,α′-dichloroalkyl radicals.

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Literature cited

  1. J. K. S. Wan, Adv. Photochem.,12, No. 4, 322 (1980).

    Google Scholar 

  2. N. N. Bubnov, A. I. Prokof'ev, A. A. Volod'kin, et al., Dokl. Akad. Nauk SSSR,210, 100 (1973).

    Google Scholar 

  3. I. V. Khudyakov and V. A. Kuz'min, Usp. Khim.,14, 1748 (1975).

    Google Scholar 

  4. J. R. Koshi, K. S. Chen, and J. K. S. Wan, Chem. Phys. Lett.,73, 557 (1980).

    Google Scholar 

  5. M. I. Kabachnik, N. N. Bubnov, S. P. Solodovnikov, and A. I. Prokof'ev, Usp. Khim.,53, 487 (1984).

    Google Scholar 

  6. G. G. Lazarev, Ya. S. Lebedev, A. I. Prokof'ev, and R. R. Rakhimov, Khim. Fiz.,3, No. 6, 867 (1984).

    Google Scholar 

  7. G. G. Lazarev, Ya. S. Lebedev, A. I. Prokof'ev, and R. R. Rakhimov, Khim. Fiz.,2, No. 4, 525 (1983).

    Google Scholar 

  8. V. B. Vol'eva, T. I. Prokof'eva, I. A. Novikova, et al., Izv. Akad. Nauk SSSR, Ser. Khim., No. 7, 1632 (1984).

    Google Scholar 

  9. A. Alberti, A. Martelli, A. Hudson, et al., J. Organomet. Chem.,182, 332 (1979).

    Google Scholar 

  10. J. K. Koshi, Adv. Free-Radical Chem.,5, 218 (1975).

    Google Scholar 

  11. A. L. J. Beckwith and K. U. Ingold, Rearrangement in Ground and Excited States, P. De Mayo (ed.), New York-London (1980).

  12. V. V. Ershov, G. A. Nikiforov, A. A. Volod'kin, Sterically Hindered Phenols [in Russian], Khimiya, Moscow (1975).

    Google Scholar 

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 822–828, April, 1989.

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Prokof'ev, A.I., Masalimov, A.S., Vol'eva, V.B. et al. EPR study of photoreduction of adducts of 3,6-di-tert-butyl-o-benzoquinone with dichlorocarbene. Russ Chem Bull 38, 738–743 (1989). https://doi.org/10.1007/BF00953283

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  • DOI: https://doi.org/10.1007/BF00953283

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