Dendritic Pillar[6]Arenes with Fixed Planar Chirality for Stereoselective Inclusions in Water: A Case of Facile Differentiation of Cocaine Adulterants, Levamisole and Dexamisole

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Publication Details

Author listBadjic̈ J.D.; Pratumyot K.; Hadad C.M.; Mortensen C.; Ward C.E.; Hansen A.R.; Politeski M.D.; Karmakar P.; Kumar N.

PublisherWiley

Publication year2025

Journal acronymAngew. Chem. Int. Ed.

Volume number64

ISSN1433-7851

eISSN1521-3773

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-105014807785&doi=10.1002%2Fanie.202514676&partnerID=40&md5=3d779f4027a16f86a6ec740f9f454287

LanguagesEnglish-Great Britain (EN-GB)


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Abstract

We describe the preparation, conformational dynamics, and stereoselective recognition characteristics of water-soluble pillar[6]arenes pS–212− and pR–212−. These two novel and diastereomeric cavitands comprise a 2,5-bis(ethoxy)pillar[6]arene core with one of six phenylene ring conjugated to two hexaanionic dendrons. Each dendron includes an (S)−glutamic acid amidated with two tris-carboxylic Behera's amines. Cavitands pS–212− and pR–212− were obtained in six synthetic steps and resolved by column chromatography. The results of 1H NMR and circular dichroism spectroscopic measurements are in line with pS/pR–212− having unidirectional orientation of alkoxy substituents (i.e., planar chirality) and no observable interconversion for, at least, 2 weeks. Computational studies supported with 1H DOSY NMR measurements revealed that sufficiently bulky dendrons require high activation energy to pass through the pillararene's cylindrical cavity therefore inhibiting rotation of the phenylene holding them. With the unique and chiral binding pocket, pS–212− (pR–212−) formed inclusion complexes with cocaine adulterants levamisole and dexamisole (Kd > mM), with their racemic mixture showing separate 1H NMR spectroscopic resonances. In this way, dendritic pillar[6]arenes can be used as chiral shift reagents for determining enantiopurity of pharmaceuticals but also for examining a variety of chiral recognition processes, sensing of chiral molecules, and stereoselective sequestrations in aqueous media. © 2025 Elsevier B.V., All rights reserved.


Keywords

DexamisoleLevamisolepillararene


Last updated on 2026-18-03 at 12:00