Literature DB >> 20165792

A fluorescent diastereoselective molecular sensor for 1,2-aminoalcohols based on the rhodamine B lactone-zwitterion equilibrium.

Clifton J Stephenson1, Ken D Shimizu.   

Abstract

A simple yet highly sensitive diastereoselective fluorescent assay was developed, which can differentiate diastereomeric 1,2-aminoalcohols such as ephedrine, pseudoephedrine, and methylephedrine using commercially available xanthene dyes. The assay is based on the rhodamine B lactone-zwitterion equilibrium, which is highly sensitive to the presence and structure of 1,2-aminoalcohols. This is in contrast to the majority of rhodamine sensors, which are based on the pH sensitive carboxylate-lactone equilibrium. A model is proposed in which the diastereoselectivity arises from the differences in the strength of an intermolecular lone pair-pi interaction within the analyte-rhodamine zwitterion complex. An assay was developed based on this sensing mechanism in which the structure and concentration of a 1,2-aminoalcohol solution can be determined using a mixture of rhodamine B and fluorescein. The selectivity and accuracy of this two-dye system was then demonstrated by the ability to measure the diastereomeric excess of samples of methylephedrine with 98% accuracy.

Entities:  

Year:  2010        PMID: 20165792     DOI: 10.1039/b918823a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Fluorescence Quenching of Xanthene Dyes during Amide Bond Formation Using DMTMM.

Authors:  Kristen N Patterson; Misael A Romero-Reyes; Jennifer M Heemstra
Journal:  ACS Omega       Date:  2022-09-07
  1 in total

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