The bicyclic N,N′-diacylaminal: A new motif for molecular self-assembly

Robert B. Grossman, Kazuyuki Hattori, Sean Parkin, Brian O. Patrick, Melissa A. Varner

Producción científica: Articlerevisión exhaustiva

12 Citas (Scopus)

Resumen

A cage-shaped N,N′-diacylaminal crystallizes from some aromatic solvents as "supramolecular chair cyclohexanes", squat cylindrical hexamers with approximate D3d symmetry containing two arene molecules, and from other aromatic and nonaromatic solvents as infinite tapes. A homologous diacylaminal crystallizes only as an infinite tape. The hexamers represent the first examples of cyclic hexamers held together by R22(8)-type hydrogen bonds in which the hydrogen-bonded atoms are not coplanar. The diacylaminal represents a new supramolecular synthon, one perhaps more suited to the design of three-dimensional architectures.

Idioma originalEnglish
Páginas (desde-hasta)13686-13687
Número de páginas2
PublicaciónJournal of the American Chemical Society
Volumen124
N.º46
DOI
EstadoPublished - nov 20 2002

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Biochemistry
  • Colloid and Surface Chemistry

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