Synthesis and conformational analysis of redox-active ferrocenyl-calixarenes

A novel synthetic approach toward redox-active calixarene-based receptors is described wherein ferrocene fragments have been introduced at the lower rim through anion-binding urea or amide connections. A thorough 1H NMR investigation on a series of calixarene-ferrocene receptors was performed in ord...

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Veröffentlicht in:Tetrahedron 2009-01, Vol.65 (3), p.672-676
Hauptverfasser: Métay, Estelle, Duclos, Marie Christine, Pellet-Rostaing, Stéphane, Lemaire, Marc, Kannappan, Ramu, Bucher, Christophe, Saint-Aman, Eric, Chaix, Carole
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container_end_page 676
container_issue 3
container_start_page 672
container_title Tetrahedron
container_volume 65
creator Métay, Estelle
Duclos, Marie Christine
Pellet-Rostaing, Stéphane
Lemaire, Marc
Kannappan, Ramu
Bucher, Christophe
Saint-Aman, Eric
Chaix, Carole
description A novel synthetic approach toward redox-active calixarene-based receptors is described wherein ferrocene fragments have been introduced at the lower rim through anion-binding urea or amide connections. A thorough 1H NMR investigation on a series of calixarene-ferrocene receptors was performed in order to estimate their hydrogen bonding-driven self-association properties and improve our understanding of the correlation between molecular structures and redox properties. [Display omitted]
doi_str_mv 10.1016/j.tet.2008.11.032
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subjects Alicyclic compounds
Alicyclic compounds, terpenoids, prostaglandins, steroids
Chemical Sciences
Chemistry
Exact sciences and technology
Organic chemistry
Preparations and properties
title Synthesis and conformational analysis of redox-active ferrocenyl-calixarenes
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