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Theoretical and Experimental Chemistry

, Volume 21, Issue 4, pp 388–397 | Cite as

Electronic structure and UV spectra of N-arylthio-1,4-benzoquinone imines

  • V. V. Pirozhenko
  • I. E. Boldeskul
  • V. T. Kolesnikov
  • L. V. Vid
  • L. O. Kuz'menko
Article
  • 61 Downloads

Abstract

The electronic structure of N-arylthio-1,4-benzoquinone imines (II) was studied by quantum-chemical methods (CNDO/2). It was shown that the special characteristics of the reactivity of the compounds in reaction with chlorine compared with sulfenylketimines R2C=N-S-Ar not containing a quinonoid ring may be due to the different nature of the lowest unoccupied molecular Orbitals (LUMO). The UV spectra of compounds (II) were investigated. In the visible region the spectra of all the compounds contain strong absorption (R1 = R2 = R3 = R4 = R5 = H, λm = 433 nm, ɛm = 2.12·104 liters/mole·cm), due to intramolecular charge transfer from the sulfur atom to the quinonoid fragment of the molecule. It was established that there is a linear relation between the energy of the transition and the σ+ constants of the substituents in the aryl fragment. The assignment of the transitions was confirmed by calculations of the UV spectra of N-arylthio-1,4-benzoquinone imines by the PPP method. Comparison of the UV spectra of these compounds with the UV spectra of N-arylsulfonyl-1,4-benzoquinone imines makes it possible to conclude that the sulfur atom of the SO2 group, unlike the divalent sulfur atom, is not capable of transmitting the electronic effects of the substituents from one part of the molecule to the other.

Keywords

Chlorine Charge Transfer Benzoquinone Linear Relation Visible Region 
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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Copyright information

© Plenum Publishing Corporation 1986

Authors and Affiliations

  • V. V. Pirozhenko
    • 1
  • I. E. Boldeskul
    • 1
  • V. T. Kolesnikov
    • 1
  • L. V. Vid
    • 1
  • L. O. Kuz'menko
    • 1
  1. 1.Institute of Organic ChemistryAcademy of Sciences of the Ukrainian SSRKiev

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