Catalysts Supported by Homochiral Molecular Helices: A New Concept to Implement Asymmetric Amplification in Catalytic Science

被引:39
|
作者
Li, Yan [1 ]
Bouteiller, Laurent [1 ]
Raynal, Matthieu [1 ]
机构
[1] Sorbonne Univ, CNRS, Inst Parisien Chim Mol, Equipe Chim Polymeres, 4 Pl Jussieu, F-75005 Paris, France
关键词
chirality amplification; asymmetric catalysis; macromolecular helices; supramolecular helices; switchable catalysis; SOLDIERS-TYPE POLY(QUINOXALINE-2,3-DIYL)S; MAIN-CHAIN; ENANTIOSELECTIVE SYNTHESIS; CHIRAL AMPLIFICATION; SELF-ASSEMBLIES; MAJORITY-RULES; POLYMER; FOLDAMERS; SERGEANTS; LIGANDS;
D O I
10.1002/cctc.201901246
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Connecting intrinsically achiral catalytic centers to helical polymers provides a new class of asymmetric catalysts whose selectivity exclusively stems from the chiral environment provided by the helical polymer. Chirality amplification phenomena allow to control the handedness and the helical sense excess of these polymers which in turn dictate the stereochemical direction and the extent of enantioinduction, respectively, obtained in the course of the asymmetric reaction. This minireview is focused on such helical catalysts built either on a covalent or a non-covalent scaffold and for which the handedness is controlled by an asymmetric polymerization reaction, by enantiopure monomers or by chiral additives. The selectivity of catalysts based on a dynamic helical backbone can be tuned by changing the solvent or with additives. The fact that the enantiomeric state of such asymmetric catalysts can be switched in a predictable way is particularly emphasized.
引用
收藏
页码:5212 / 5226
页数:15
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