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Chemistry of Heterocyclic Compounds

, Volume 1, Issue 1, pp 49–53 | Cite as

Infrared spectra of pyrroles and dipyrrylmethanes

  • A. F. Mironov
  • L. D. Miroshnichenko
  • R. P. Evstigneeva
  • N. A. Preobrazhenskii
Article
  • 369 Downloads

Abstract

The IR spectra of 18 substituted pyrroles and 6 substituted dipyrrylmethanes are investigated. It is shown that the position of the valence vibrations frequency of the free NH group, νfree NH depends on the number of substituents in the ring. The frequency is influenced by the electronegativity of a substituent, the effect of an α- being much more marked than that of a β-substituent. The stability of the hydrogen bond increases with increase in substituent electronegativity. When two electronegative substituents occupy the α and β positions, they have a mutually weakening effect. The νC=O (acetyl) absorption bands in pyrrolecontaining compounds are situated 40–60 cm−1 lower than in aromatic ketones and greatly depend on the position and nature of the substituent in the pyrrole ring.

Keywords

Hydrogen Hydrogen Bond Absorption Band Ketone Acetyl 
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

© The Faraday Press, Inc. 1965

Authors and Affiliations

  • A. F. Mironov
    • 1
  • L. D. Miroshnichenko
    • 1
  • R. P. Evstigneeva
    • 1
  • N. A. Preobrazhenskii
    • 1
  1. 1.Lomonosov Institute of Fine Chemical TechnologyMoscow

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