Probing the Chiroptical Response of a Single Molecule

  • Ruthanne Hassey
    Department of Chemistry, University of Massachusetts-Amherst, Amherst, MA 01003, USA.
  • Ellen J. Swain
    Department of Chemistry, University of Massachusetts-Amherst, Amherst, MA 01003, USA.
  • Nathan I. Hammer
    Department of Chemistry, University of Massachusetts-Amherst, Amherst, MA 01003, USA.
  • Dhandapani Venkataraman
    Department of Chemistry, University of Massachusetts-Amherst, Amherst, MA 01003, USA.
  • Michael D. Barnes
    Department of Chemistry, University of Massachusetts-Amherst, Amherst, MA 01003, USA.

書誌事項

公開日
2006-12
DOI
  • 10.1126/science.1134231
公開者
American Association for the Advancement of Science (AAAS)

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説明

<jats:p> Chirally sensitive measurement techniques have generally been restricted to bulk samples. Here, we report the observation of fluorescence-detected circular dichroism (FDCD) from single (bridgedtriarylamine) helicene molecules by using an excitation wavelength (457 nanometers) in the vicinity of an electronic transition that shows circular dichroism in bulk samples. The distributions of dissymmetry ( <jats:italic>g</jats:italic> ) parameters by analysis of signals from pure <jats:italic>M</jats:italic> - and <jats:italic>P</jats:italic> -type diastereomers are almost perfect mirror images of one another, each spanning a range of both positive and negative values. In addition, we observe a well-defined structure in the histogram of dissymmetry parameters suggestive of specific molecular orientations at the polymer interface. These single-molecule results highlight strong intrinsic circular dichroism responses that can be obscured by cancellation effects in ensemble measurements of a randomly oriented bulk sample. </jats:p>

収録刊行物

  • Science

    Science 314 (5804), 1437-1439, 2006-12

    American Association for the Advancement of Science (AAAS)

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