New azobenzene crown ether p-tert-butylcalix [4]arenes (6 and 7) have been synthesized by reductive coupling reactions between two nitrobenzene groups. Their isomerization and switchable binding properties towards Na + and K + were studied by 1 H NMR spectroscopy. The results showed that Na + prefer
✦ LIBER ✦
ChemInform Abstract: New Azobenzene Crown p-tert-Butylcalix[4]arenes as Switchable Receptors for Na+ and K+ Ions: Synthesis and Isomerization Studies.
✍ Scribed by Bongkot Pipoosananakaton; Mongkol Sukwattanasinitt; Nongnuj Jaiboon; Narongsak Chaichit; Thawatchai Tuntulani
- Book ID
- 101906951
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 29 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
📜 SIMILAR VOLUMES
Preparation of new azobenzene crown ethe
✍
Bongkot Pipoosananakaton; Mongkol Sukwattanasinitt; Nongnuj Jaiboon; Narongsak C
📂
Article
📅
2000
🏛
Elsevier Science
🌐
French
⚖ 110 KB