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Experimental and Theoretical Study of the Complexation of Cesium and Thallium Cations by a Water‐Soluble Cryptophane
Author(s) -
Chapellet LaureLise,
Dog JeanPierre,
Jean Marion,
Vanthuyne Nicolas,
Berthault Patrick,
Buffeteau Thierry,
Brotin Thierry
Publication year - 2017
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201700979
Subject(s) - chemistry , thallium , molecule , caesium , aqueous solution , titration , computational chemistry , inorganic chemistry , organic chemistry
Cs (cesium) and Tl (thallium) are known to be very toxic for the environment and human health. Thus, the synthesis of molecular receptors aimed at extracting these two elements from the environment is strongly desired. In this article, we report the synthesis of the two enantiomers of a water‐soluble cryptophane‐223 ( 1 ) and the study of their interaction with cesium and thallium cations in basic aqueous solutions. These two complexes have been studied by 133 Cs and 205 Tl NMR spectroscopy to reveal the complexation of the two metallic cations and by chiroptical techniques (electronic and vibrational circular dichroism) to provide valuable information about the conformational changes occurring during the binding process. The thermodynamic parameters of complexation K , ΔH 0 and ΔS 0 obtained from titration experiments reveal a strong interaction between 1 and the two cations under a large range of experimental conditions. A decomposition of the total binding energy, performed by DFT calculations, allows us to characterize the nature of the interactions existing between the cage‐molecule and these two cations. These calculations also reveal the importance of the spin‐orbit coupling for predicting correctly the large frequency difference between the free Tl + and Tl + @ 1 NMR signals and to understand its origin. In addition to the development of a methodology enabling detailed understanding of the host‐guest interaction, this study indicates a very pronounced selectivity of this cage‐molecule towards both Cs + and Tl + cations in various experimental conditions.