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Crystal and molecular structures of benz-p-nitroanilide and benz-p-methoxyanilide

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Abstract

The crystal structures of the two carboxylic amides C13H10N2O3 (I) and C14H13NO2 (II) have been determined by direct methods and refined by full-matrix least squares. The predominant structural feature is the hydrogen bonding (N-H⋯O=C) which influences the conformations of both structures.

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Author notes

  1. Michael P. Du Plessis

    Present address: School of Chemical Sciences, University of Cape Town, 7700, Rondebosch, South Africa

Authors and Affiliations

  1. A.E.C.I. Research Department, Explosives Division, 1645, North Rand, South Africa

    Michael P. Du Plessis, Tomasz A. Modro & Luigi R. Nassimbeni

Authors
  1. Michael P. Du Plessis
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  2. Tomasz A. Modro
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  3. Luigi R. Nassimbeni
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Du Plessis, M.P., Modro, T.A. & Nassimbeni, L.R. Crystal and molecular structures of benz-p-nitroanilide and benz-p-methoxyanilide. Journal of Crystallographic and Spectroscopic Research 13, 179–189 (1983). https://doi.org/10.1007/BF01161512

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  • DOI: https://doi.org/10.1007/BF01161512

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