Noncovalent interactions in high-performance liquid chromatography enantioseparations on polysaccharide-based chiral selectors.

Chiral recognition High-performance liquid chromatography Molecular modelling Noncovalent interactions Polysaccharide-based chiral stationary phases

Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
19 Jul 2020
Historique:
received: 26 03 2020
revised: 02 05 2020
accepted: 04 05 2020
entrez: 8 6 2020
pubmed: 9 6 2020
medline: 13 8 2020
Statut: ppublish

Résumé

Designed more than thirty years ago in order to improve and maximize the discrimination capability of native polysaccharides, cellulose- and amylose-based selectors have shown excellent and unequalled performances for the enantioseparation of chiral compounds. The successful story of these chiral selectors relies on a multi-site high-ordered chiral platform which is held up by intramolecular hydrogen bonds (HBs), and makes the polymer able to host and discriminate enantiomers. In this environment, both achiral and stereoselective intermolecular noncovalent interactions play a pivotal role, and HBs, halogen bonds (XBs), dipole-dipole, π-π stacking, steric repulsive, and van der Waals interactions underlie adsorption process and formation of transient diastereomeric assemblies between the polymer and the enantiomer pair. In the last decades, advances in computational chemistry and spectroscopic techniques have improved knowledge of noncovalent interactions, contributing to decode their functions in chemical systems. Significantly, over time the growing interplay between experimental and theoretical approaches has contributed to unravel intermolecular forces underlying selector-selectand association and to understand recognition patterns. On this basis, this review summarizes seminal and representative studies dealing with noncovalent interactions that function in HPLC enantioseparations promoted by cellulose benzoates and phenylcarbamates of amylose and cellulose. The importance of integrating theoretical and experimental approaches to profile mechanisms and interaction patterns is highlighted by discussing focused case studies. In particular, the advantageous utilization of electrostatic potential (V) analysis and molecular dynamics (MD) simulations in this field is evidenced. A systematic compilation of all published literature has not been attempted.

Identifiants

pubmed: 32505290
pii: S0021-9673(20)30466-0
doi: 10.1016/j.chroma.2020.461202
pii:
doi:

Substances chimiques

Phenylcarbamates 0
Polysaccharides 0
Cellulose 9004-34-6

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

461202

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Paola Peluso (P)

Istituto di Chimica Biomolecolare ICB, CNR, Sede secondaria di Sassari, Traversa La Crucca 3, Regione Baldinca, I-07100 Li Punti - Sassari, Italy. Electronic address: paola.peluso@cnr.it.

Victor Mamane (V)

Institut de Chimie de Strasbourg, UMR CNR 7177, Equipe LASYROC, 1 rue Blaise Pascal, 67008 Strasbourg Cedex, France.

Roberto Dallocchio (R)

Istituto di Chimica Biomolecolare ICB, CNR, Sede secondaria di Sassari, Traversa La Crucca 3, Regione Baldinca, I-07100 Li Punti - Sassari, Italy.

Alessandro Dessì (A)

Istituto di Chimica Biomolecolare ICB, CNR, Sede secondaria di Sassari, Traversa La Crucca 3, Regione Baldinca, I-07100 Li Punti - Sassari, Italy.

Sergio Cossu (S)

Dipartimento di Scienze Molecolari e Nanosistemi DSMN, Università Ca' Foscari Venezia, Via Torino 155, 30172 Mestre Venezia, Italy.

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Classifications MeSH