4.7 Article

Semiquantitative Visual Chiral Assay with a Pseudoenantiomeric Fluorescent Sensor Pair

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 86, Issue 14, Pages 9603-9609

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c00875

Keywords

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Funding

  1. Sichuan Science and Technology Program [2021YJ0398]
  2. US National Science Foundation [CHE1855443]

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A new red-light-emitting fluorescent probe (R)-5 was synthesized, showing good enantioselective fluorescence enhancement in the presence of Zn2+ and when combined with a green-light-emitting probe (S)-4 formed a pseudoenantiomeric sensor pair. This sensor pair can detect both enantiomers of chiral amino acids simultaneously at two very different wavelengths.
A new red-light-emitting fluorescent probe (R)-5 was synthesized. In the presence of Zn2+, this compound was found to exhibit good enantioselective fluorescence enhancement at lambda = 655 nm when treated with a variety of amino acids in aqueous solution. This probe in combination with a green-light-emitting probe (S)-4 that has enantioselective fluorescence enhancement at lambda = 505 nm has formed a pseudoenantiomeric sensor pair because of their opposite enantioselectivities. This sensor pair can simultaneously detect both enantiomers of a chiral amino acid at two very different wavelengths (Delta = 150 nm). It was used to visually and semiquantitatively determine the enantiomeric compositions of amino acids. For example, when a 1:1 mixture of (R)-5 and (S)-4 was treated with Zn(OAc)(2) and histidine samples of 0-100% [D-His], the color of the mixtures changed from green to yellow, orange, and red under a UV lamp (365 nm), which allowed a quick quantification of [D-His]%. This is the first example of using fluorescence to visually quantify the enantiomeric composition of chiral compounds.

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