Issue 5, 1994
From the journal:

Journal of the Chemical Society, Perkin Transactions 2

Analysis of the conformational behaviour of perfunctionalized β-cyclodextrins. Part 1. Evidence for insertion of one of the rim substituents into the cyclodextrin cavity in organic solvents

Ludovic Jullien,   Josette Canceill,   Liliane Lacombe  and  Jean-Marie Lehn  

Abstract

Several functionalized β-cyclodextrins have been shown to exhibit conformational isomerism. The analysis of the conformational behaviour of several derivatives strongly suggests that a slow exchange occurs between C7 and C1 conformers, the C1 probably involving insertion of one of the primary rim substituents in the cyclodextrin cavity. The significance of the structural features of cyclodextrin substituents for the occurrence of conformational isomerism is examined. The relevance of the use of cyclodextrins for the design of molecular devices is discussed.

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Article information

DOI
https://doi.org/10.1039/P29940000989
Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1994, 989-1002

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Analysis of the conformational behaviour of perfunctionalized β-cyclodextrins. Part 1. Evidence for insertion of one of the rim substituents into the cyclodextrin cavity in organic solvents

L. Jullien, J. Canceill, L. Lacombe and J. Lehn, J. Chem. Soc., Perkin Trans. 2, 1994, 989 DOI: 10.1039/P29940000989

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