Coordination of Co2+ Ions in the Interior of Poly(propylene amine) Dendrimers Containing Fluorescent Dansyl Units in the Periphery

We have investigated the interaction of Co2+ ions (as nitrate salt) with dendrimers of the poly(propylene amine) family functionalized in the periphery with fluorescent dansyl units. Each dendrimer n D, where the generation number n goes from 1 to 5, comprises 2( n +1) dansyl functions in the periph...

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Published inJournal of the American Chemical Society Vol. 122; no. 42; pp. 10398 - 10404
Main Authors Vögtle, Fritz, Gestermann, Sven, Kauffmann, Christopher, Ceroni, Paola, Vicinelli, Veronica, Balzani, Vincenzo
Format Journal Article
LanguageEnglish
Published American Chemical Society 25.10.2000
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Summary:We have investigated the interaction of Co2+ ions (as nitrate salt) with dendrimers of the poly(propylene amine) family functionalized in the periphery with fluorescent dansyl units. Each dendrimer n D, where the generation number n goes from 1 to 5, comprises 2( n +1) dansyl functions in the periphery and 2( n +1) − 2 tertiary amine units in the interior. For comparison purposes, the behavior of a monodansyl reference compound (I) has also been investigated. The results obtained have shown that:  (i) the absorption and fluorescence spectra of the reference compound I are not affected by addition of Co2+ ions; (ii) in the case of the dendrimers, the absorption spectra are unaffected, but a strong quenching of the fluorescence of the peripheral dansyl units is observed; (iii) the fluorescence quenching takes place by a static mechanism involving coordination of metal ions in the interior of the dendrimers; (iv) metal ion coordination by the dendrimers is a fully reversible process; (v) a strong amplification of the fluorescence quenching signal is observed with increasing dendrimer generation. For the larger dendrimers (n = 3, 4, and 5), at very low metal ion concentration 1:1 metal/dendrimer species are formed, in which the Co2+ ion guest quenches each one of the dansyl units that becomes excited after light absorption.
Bibliography:ark:/67375/TPS-1WVKDQ2R-D
istex:815341DA7B93443AE2A587F94B28D09588C93E6B
ISSN:0002-7863
1520-5126
DOI:10.1021/ja993745h