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Effect of nature of substituents on photochemical behavior of 2,6-disubstituted 1,4-benzoquinones

  • B. D. Sviridov
  • L. P. Gryzunova
  • V. M. Kuznets
  • G. A. Nikiforov
  • K. De Jonge
  • H. J. Hageman
  • V. V. Ershov
Brief Communications
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Conclusions

  1. 1.

    We studied the photochemical transformations of some 2,6-disubstituted 1,4-benzoquinones in aliphatic alcohols, acetic acid, and aromatic hydrocarbons.

     
  2. 2.

    In aliphatic alcohols the photolysis of the quinones leads to the formation of only reduction products, whereas in acetic acid and aromatic hydrocarbons the nature of the substituents exerts a substantial effect on the structure of the end reaction products.

     

Keywords

Alcohol Acetic Acetic Acid Hydrocarbon Quinone 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

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    A. V. El'tsov, O. P. Studzinskii,and V. M. Grebenkina, Usp. Khim.,46, 185 (1977).Google Scholar
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    H. J. Hageman, Methoden der Organischen Chemie, Vol. 4/5b, Photochemie (1976), p. 941.Google Scholar
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    S. Patai (editor), The Chemistry of Quinonoid Compounds, Vol. 1, Hebrew University, Jerusalem, Israel (1974).Google Scholar
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    C. M. Orlando, Jr., H. Mark, A. K. Bose, and M. S. Manhas, J. Am. Chem. Soc.,89, 6257 (1967).Google Scholar
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Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • B. D. Sviridov
    • 1
    • 2
    • 3
  • L. P. Gryzunova
    • 1
    • 2
    • 3
  • V. M. Kuznets
    • 1
    • 2
    • 3
  • G. A. Nikiforov
    • 1
    • 2
    • 3
  • K. De Jonge
    • 1
    • 2
    • 3
  • H. J. Hageman
    • 1
    • 2
    • 3
  • V. V. Ershov
    • 1
    • 2
    • 3
  1. 1.Institute of Chemical PhysicsAcademy of Sciences of the USSRMoscow
  2. 2.L. Ya. Karpov Physicochemical InstituteMoscow
  3. 3.AKZO Research LaboratoriesArnhemNetherlands

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