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Detection of Boronic Acids through Excited-State Intramolecular Proton-Transfer Fluorescence
Organic Letters (2013)
  • Matthew R. Aronoff, University of Wisconsin - Madison
  • Brett VanVeller, University of Wisconsin - Madison
  • Ronald T. Raines, University of Wisconsin - Madison
Abstract

Boronic acids are versatile reagents for the chemical synthesis of organic molecules. They and other boron-containing compounds can be detected readily by the interruption of the excited-state intramolecular proton transfer (ESIPT) of 10-hydroxybenzo[h]quinolone. This method is highly sensitive and selective, and useful for monitoring synthetic reactions and detecting boron-containing compounds on a solid support.

Keywords
  • boronic acid derivative,
  • proton,
  • quinolone derivative,
  • chemical structure,
  • chemistry,
  • fluorescence,
  • molecular structure
Disciplines
Publication Date
October, 2013
Publisher Statement
Reprinted (adapted) with permission from Organic Letters 15 (2013): 5382, doi: 10.1021/ol402714k. Copyright 2013 American Chemical Society.
Citation Information
Matthew R. Aronoff, Brett VanVeller and Ronald T. Raines. "Detection of Boronic Acids through Excited-State Intramolecular Proton-Transfer Fluorescence" Organic Letters Vol. 15 Iss. 20 (2013)
Available at: http://works.bepress.com/brett_vanveller/3/