Abstract
A photoresponsive crown ether which combines within a molecule both a crown ether and a photoisomerizable functional group changes the conformation of the crown ring in response to photoirradiation. Thus, many chemical and physical functions of the crown ether family can be controlled by on-off light switch. The syntheses and the functions (ion extraction, ion transport, etc.) of following photoresponsive crown ethers are described: azobenzene-bridged crown ethers, crown ethers containing azobenzene as a ring member, azobis(benzocrown ether)s, and anthracene-containing crown ethers. In relation to the cis-trans isomerism of azobenzene, the mechanism of thermal cis-to-trans isomerization is discussed.
Original language | English |
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Pages (from-to) | 92-101 |
Number of pages | 10 |
Journal | Journal of Synthetic Organic Chemistry, Japan |
Volume | 40 |
Issue number | 2 |
DOIs | |
Publication status | Published - Jan 1982 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Organic Chemistry