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Peripheral mechanism for hydrogenation of aromatic nitro compounds: Reaction of nitrobenzene with copper(II)-alizarin complex

  • A. V. Bulatov
  • A. N. Kitaigorodskii
  • A. V. Letuchaya
  • A. T. Nikitaev
  • A. N. Shupik
  • M. L. Khidekel'
Brief Communications
  • 39 Downloads

Conclusions

Nitrobenzene forms a molecular complex with copper bis(alizarinate) in which the nitro group is oriented in a direction opposite to the metal ion.

Keywords

Hydrogenation Copper Nitrobenzene Nitro Group Alizarin 
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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    E. G. Chepaikin and M. L. Khidekel', J. Mol. Catal.,4, 103 (1978).Google Scholar
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    A. V. Bulatov and M. L. Khidekel', Trans. Met. Chem.,5, 123 (1980).Google Scholar
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    A. V. Bulatov, E. G. Chepaikin, and M. L. Khidekel', Proceedings of Nineteenth International Conference on Coordination Chemistry, Prague (1978), p. 23.Google Scholar
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    A. V. Bulatov and K. E. Gol'dshmidt, in: Kinetics of Physicochemical Reactions [in Russian], Chernogolvka (1980), p. 19.Google Scholar
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    A. V. Bulatov, R. N. Lobkovskaya, M. L. Khidekel', A. N. Chekhlov, and R. P. Shibaeva, Izv. Akad. Nauk SSSR, Ser. Khim.,1980, 1203.Google Scholar
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    A. N. Kitaigorodskii, V. M. Nekipelov, and K. I. Zamaraev, Zh. Strukt. Khim.,19, 798 (1978).Google Scholar

Copyright information

© Plenum Publishing Corporation 1981

Authors and Affiliations

  • A. V. Bulatov
    • 1
  • A. N. Kitaigorodskii
    • 1
  • A. V. Letuchaya
    • 1
  • A. T. Nikitaev
    • 1
  • A. N. Shupik
    • 1
  • M. L. Khidekel'
    • 1
  1. 1.Branch of Institute of Chemical PhysicsAcademy of Sciences of the USSRChernogolovka

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