Molecular building blocks: chromophoric amphiphilic cyclodextrin derivatives
- 1 May 1994
- journal article
- research article
- Published by Taylor & Francis in Supramolecular Chemistry
- Vol. 3 (3) , 171-173
- https://doi.org/10.1080/10610279408028911
Abstract
The primary hydroxyl face of β-cyclodextrin can be selectively modified with ortho-, meta-, and para-nitro-thiophenol groups. Rigid alignment of the chromophoric groups has been obtained in the formation of mono-molecular layers at the air-water interface.Keywords
This publication has 7 references indexed in Scilit:
- Supramolecular assemblies based on amphiphilic cyclodextrinsSupramolecular Chemistry, 1993
- Self‐organizing systems based on amphiphilic cyclodextrin diestersJournal of Physical Organic Chemistry, 1992
- Cyclodextrins, Off‐the‐Shelf Components for the Construction of Mechanically Interlocked Molecular SystemsAngewandte Chemie International Edition in English, 1992
- Self-assembling systems of the amphiphilic cationic per-6-amino-.beta.-cyclodextrin 2,3-di-O-alkyl ethersJournal of the American Chemical Society, 1992
- Formation of amphiphilic cyclodextrins via hydrophobic esterification at the secondary hydroxyl faceTetrahedron Letters, 1991
- Association between amphiphilic cyclodextrins and cholesterol in mixed insoluble monolayers at the air-water interfaceLangmuir, 1989
- Photoisomerization of the azobenzenes included in Langmuir-Blodgett films of cyclodextrinsThin Solid Films, 1988