Abstract
The macrocyclic amphiphile 1 and 2 through electrostatic interactions were synthesized from their cationic and anionic components in a flask and on a water subphase. The macrocyclic amphiphiles formed stable floating monolayers on a water subphase, where the limiting areas were decisively determined by the cross-sectional areas of the tetracationic cyclophane moieties, leading to the enhancement of photoisomerizability of azobenzene units in monolayers.
| Original language | English |
|---|---|
| Pages (from-to) | 314-315 |
| Number of pages | 2 |
| Journal | American Chemical Society, Polymer Preprints, Division of Polymer Chemistry |
| Volume | 39 |
| Issue number | 2 |
| Publication status | Published - 1998 Aug 1 |
| Externally published | Yes |
| Event | Proceedings of the 1997 Boston Meeting - Boston, MA, USA Duration: 1998 Aug 23 → 1998 Aug 27 |
ASJC Scopus subject areas
- Polymers and Plastics