Related Experiment Video
Updated: Feb 3, 2026

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
Published on: September 6, 2019
Recognition of Oligosaccharides by Chirality Induced in Europium (III) Compounds
Tao Wu1, Jiří Kessler1, Jakub Kaminský1
1Department of Molecular Spectroscopy, Institute of Organic Chemistry and Biochemistry, The Czech Academy of Sciences, Flemingovo nám. 2, Prague, 16610, Czech Republic.
Abstract:
Identification of saccharides is difficult due to their similar chemical structure. However, they interact very selectively with lanthanide probes. To explore the potential for saccharide recognition, we compare circularly polarized luminescence induced by a variety of oligo- and polysaccharides in three europium compounds. Measurement on a standard Raman optical activity spectrometer made it possible to use high excitation powers and provided very distinct spectral patterns, which were sensitive both to the local structure and differences in molecular size. For example, α-, β- and γ-cyclodextrins provided unique spectroscopic responses. Titration data and molecular dynamics simulation confirmed that CPL spectra carry information about the binding mode and strength between the lanthanide probe and saccharide skeleton.
Related Concept Videos
Oligosaccharide Assembly
Multiple sugar molecules that may or may...
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Coordination Compounds and Nomenclature
Chirality in Nature
Ionic Compounds: Formulas and Nomenclature
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...

