抄録
A photoresponsive surfactant with a cationic azobenzene head group (I) was synthesized. It was demonstrated that by mixing (I) with a conventional cationic micelle the rate of the micelle-catalyzed reaction (base-catalyzed proton abstraction from benzoin) can be controlled by light. The origin of the photocontrol was accounted for by the difference in the partitioning of trans-(I) and cis-(I) in the micelle phase.
本文言語 | 英語 |
---|---|
ページ(範囲) | 1409-1412 |
ページ数 | 4 |
ジャーナル | Tetrahedron Letters |
巻 | 22 |
号 | 15 |
DOI | |
出版ステータス | 出版済み - 1981 |
外部発表 | はい |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry