| Literature DB >> 15330619 |
Abstract
[structure: see text] When four facially amphiphilic cholate derivatives are attached to a tetraaminocalixarene scaffold, the resulting molecule responds to environmental changes by rotation of the cholate units. In polar solvents, the molecule adopts a micellelike conformation with the hydrophilic alpha-faces of the cholates pointing outward. In nonpolar solvents, it turns inside out, assuming a reversed micellelike conformation with the hydrophobic beta-faces pointing outward. Switching between the two conformations is driven by solvophobic interactions and is fully reversible.Entities:
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Year: 2004 PMID: 15330619 DOI: 10.1021/ol048679p
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005