Gels (Apr 2018)

Non-Steroidal Biphenyl Gelators: Correlation of Xerogel Structure with Solid-State Structure and Circular Dichroism Spectroscopy

  • H. Cristina Geiger,
  • David K. Geiger,
  • William R. Roberts,
  • Dominic L. Morell,
  • Paul Huttunen,
  • Jennifer L. Schulman,
  • Melanie Tran,
  • Dori Farthing

DOI
https://doi.org/10.3390/gels4020034
Journal volume & issue
Vol. 4, no. 2
p. 34

Abstract

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Because the factors favoring the formation of well-formed single crystals are dissimilar to those conducive to gel formation, few examples of single-crystal structural characterizations of organogelators are found in the literature. A series of biphenyl methyl and ethyl diester derivatives of varying chain length were synthesized and their gelation abilities explored. X-ray diffraction of single crystals of one of the gelators reveals a columnar extended structure. Based on XRD results for xerogels obtained from the reported organogelators, the members of the series are isostructural and so also adopt a columnar superstructure. Scanning electron microscopy (SEM) was used for the investigation of the morphology of the xerogels, which display either platelet-like morphologies or more typical entangled twisted ribbon-like aggregates. The gels exhibit chirality, which depends on the sol-gel transition history, as observed by induced circular dichroism (ICD) spectroscopy.

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