𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photo-Cleavable Cryptands: Synthesis and Structure

✍ Scribed by Ralf Warmutha; Ernst Grell; Jean-Marie Lehn; Jan W. Bats; Gerhard Quinkert


Publisher
John Wiley and Sons
Year
1991
Tongue
German
Weight
691 KB
Volume
74
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The four photo‐cleavable ligands 1–4 of the macrobicyclic‐cryptand type have been synthesized by introducing a photo‐sensitive 2‐nitrobenzyl‐ or 4,5‐dimethoxy‐2‐nitrobenzyl‐ether bond into one of the bridges. These compounds are expected to retain the selective binding features of the parent cryptands and to allow the photolytically induced release of alkali ions in aqueous solution. The crystal structures of the ligand 5‐(2‐nitro‐phenyl)‐4,7,13,16,21,24‐hexaoxa‐1,10‐diazabicyclo[8.8.8]hexacosane (3) and of its KSCN complex 13 have been determined. They are analogous to those of the corresponding parent species, confirming the macrobicyclic geometry and the cryptate nature of the complex. Spectroscopic properties are reported.


📜 SIMILAR VOLUMES


ChemInform Abstract: Cryptands by One-Po
✍ Flavia Piron; Crina Cismas; Anamaria Terec; Jean Roncali; Ion Grosu 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 15 KB

## 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 v

Caro-Cryptands: Tris-carotenoid macrobic
✍ Jean-Marie Lehn; Jean-Pierre Vigneron; Itka Bkouche-Waksman; Jean Guilhem; Claud 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 482 KB

The tris-carotenoid macrobicycles 1 and 2 were obtained in good yields in a one-step macrobicyclisation condensation between the tripode N(CH,CH2NH2), and the polyolefinic dialdehydes 5 and 6. They form dinuclear cryptates by complexation of two Cu' ions. The crystal structure of the tris-carotenoid