Recognition in the Domain of Molecular Chirality: From Noncovalent Interactions to Separation of Enantiomers

被引:140
|
作者
Peluso, Paola [1 ]
Chankvetadze, Bezhan [2 ]
机构
[1] CNR, Ist Chim Biomol ICB, Sede Secondaria Sassari, I-07100 Sassari, Italy
[2] Tbilisi State Univ, Inst Phys & Analyt Chem, Sch Exact & Nat Sci, GE-0179 Tbilisi, Georgia
关键词
PERFORMANCE LIQUID-CHROMATOGRAPHY; NUCLEAR-MAGNETIC-RESONANCE; VAN-DER-WAALS; SUPERCRITICAL-FLUID CHROMATOGRAPHY; ABSOLUTE ASYMMETRIC-SYNTHESIS; METAL-ORGANIC FRAMEWORKS; CYCLODEXTRIN INCLUSION COMPLEXES; SELECTOR-SELECTAND INTERACTIONS; CAPILLARY GAS-CHROMATOGRAPHY; NATIVE BETA-CYCLODEXTRIN;
D O I
10.1021/acs.chemrev.1c00846
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is not a coincidence that both chirality and noncovalent interactions are ubiquitous in nature and synthetic molecular systems. Noncovalent interactivity between chiral molecules underlies enantioselective recognition as a fundamental phenomenon regulating life and human activities. Thus, noncovalent interactions represent the narrative thread of a fascinating story which goes across several disciplines of medical, chemical, physical, biological, and other natural sciences. This review has been conceived with the awareness that a modern attitude toward molecular chirality and its consequences needs to be founded on multidisciplinary approaches to disclose the molecular basis of essential enantioselective phenomena in the domain of chemical, physical, and life sciences. With the primary aim of discussing this topic in an integrated way, a comprehensive pool of rational and systematic multidisciplinary information is provided, which concerns the fundamentals of chirality, a description of noncovalent interactions, and their implications in enantioselective processes occurring in different contexts. A specific focus is devoted to enantioselection in chromatography and electromigration techniques because of their unique feature as "multistep" processes. A second motivation for writing this review is to make a clear statement about the state of the art, the tools we have at our disposal, and what is still missing to fully understand the mechanisms underlying enantioselective recognition.
引用
收藏
页码:13235 / 13400
页数:166
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