Synthesis of interlocked diazacoronand system

Citation
P. Tarnowski et al., Synthesis of interlocked diazacoronand system, SUPRAMOL CH, 12(2), 2000, pp. 217-219
Citations number
9
Categorie Soggetti
Chemistry
Journal title
SUPRAMOLECULAR CHEMISTRY
ISSN journal
10610278 → ACNP
Volume
12
Issue
2
Year of publication
2000
Pages
217 - 219
Database
ISI
SICI code
1061-0278(2000)12:2<217:SOIDS>2.0.ZU;2-T
Abstract
New 2,9-disubstituted 1,10-phenanthroline derivatives have been obtained, r etaining the ability to form stable complexes with transition metals. Due t o special, pseudotetrahedral topography of the copper(I) complexes the subs equent ring formation reaction can lead to copper(I) catenates. Thus, the k nown 2,9-bis(p-hydroxyphenyl)-1,10-phenanthroline ligand, was elongated by the reaction with tert-butyl bromoacetate, forming a diester capable of und ergoing a double amidation reaction. Such synthetic strategy can provide th e corresponding diazacoronands as well as amide-containing interlocked cate nane systems, when a three-dimensional template effect of copper atom is em ployed.