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Planarity of Nitro-Substituted Phenothiazines

  • Carolyn Pratt Brock
  • , Paul J. DeLaLuz
  • , Miroslaw Golinski
  • , Michael A. Lloyd
  • , Thomas C. Vanaman
  • , David S. Watt

Producción científica: Articlerevisión exhaustiva

6 Citas (Scopus)

Resumen

The structures of three nitro-substituted phenothiazines [1,3,4-trifluoro-2-nitrophenothiazine, 10-(4-chlorobutyl)-1,3,4-trifluoro-2-nitrophenothiazine and 10-(4-chlorobutyl)-3-nitrophenothiazine] have been determined. The first of these red compounds forms infinite stacks in the solid state, in which donor and acceptor regions of the approximately planar molecules alternate. The molecules of the other two compounds, which have folded, or 'butterfly', conformations in the solid state, do not form stacks, presumably because the bulky chlorobutyl substituents cannot be accommodated. The very dark color of solid 3-nitrophenothiazine suggests the presence of extended molecular stacks, but crystals suitable for a structure determination could not be obtained.

Idioma originalEnglish
Páginas (desde-hasta)713-719
Número de páginas7
PublicaciónActa Crystallographica Section B: Structural Science
Volumen52
N.º4
DOI
EstadoPublished - ago 1 1996

Financiación

FinanciadoresNúmero del financiador
National Institute of General Medical SciencesR01GM047427

    ASJC Scopus subject areas

    • General Biochemistry, Genetics and Molecular Biology

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