Work

A large conformational change of a bridged beta-cyclodextrin dimer in aqueous solution

Year: 2003

Type: article

Abstract: A novel bridged P-CD dimer in which two beta-cyclodextrins were linked by a naphthalene at positions 2 and 7 has been synthesized. H-1 and (CNMR)-C-13 measurements showed that a large change in the conformation of the dimer occurred in aqueous solution. The dimer interacted with methyl and ethyl orange to form stable inclusion complexes via "induced fit" mechanism.

Source: Lanzhou University Institutional Repository

Authors: X-Q Zheng, YuHuang Wang, QX Guo, Lu Yang, YC Liu

Language: English

Topic: Supramolecular Chemistry and Complexes

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: green

OpenAlex ID: W2340504940

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