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Synthesis of a Mechanically Planar Chiral Rotaxane Ligand for Enantioselective Catalysis.

ABSTRACT: Rotaxanes are interlocked molecules in which a molecular ring is trapped on a dumbbell-shaped axle because of its inability to escape over the bulky end groups, resulting in a so-called mechanical bond. Interlocked molecules have mainly been studied as components of molecular machines, but the crowded, flexible environment created by threading one molecule through another has also been explored in catalysis and sensing. However, so far, the applications of one of the most intriguing properties of interlocked molecules, their ability to display stereogenic units that do not rely on the stereochemistry of their covalent subunits, termed "mechanical chirality," have yet to be properly explored, and prototypical demonstration of the applications of mechanically chiral rotaxanes remain scarce. Here, we describe a mechanically planar chiral rotaxane-based Au complex that mediates a cyclopropanation reaction with stereoselectivities that are comparable with the best conventional covalent catalyst reported for this reaction.

SUBMITTER: Heard AW

PROVIDER: S-EPMC7153771 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Synthesis of a Mechanically Planar Chiral Rotaxane Ligand for Enantioselective Catalysis.

Heard Andrew W AW Goldup Stephen M SM

Chem 20200409 4

Rotaxanes are interlocked molecules in which a molecular ring is trapped on a dumbbell-shaped axle because of its inability to escape over the bulky end groups, resulting in a so-called mechanical bond. Interlocked molecules have mainly been studied as components of molecular machines, but the crowded, flexible environment created by threading one molecule through another has also been explored in catalysis and sensing. However, so far, the applications of one of the most intriguing properties o ...[more]

PMID: 32309674

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