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

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    Coordination of Co2+ Ions in the Interior of Poly(propylene amine) Dendrimers Containing Fluorescent Dansyl Units in the Periphery
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    Contribution from the Kekulé-Institut für Organische Chemie und Biochemie der Universität Bonn, Gerhard-Domagk Strasse 1, D-53121 Bonn, Germany, and Dipartimento di Chimica “G. Ciamician”, Università di Bologna, via Selmi 2, I-40126 Bologna, Italy
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    Cite this: J. Am. Chem. Soc. 2000, 122, 42, 10398–10404
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    https://doi.org/10.1021/ja993745h
    Published October 7, 2000
    Copyright © 2000 American Chemical Society
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    Abstract

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    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 nD, 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.

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     Universität Bonn.

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     Università di Bologna.

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    Cite this: J. Am. Chem. Soc. 2000, 122, 42, 10398–10404
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    https://doi.org/10.1021/ja993745h
    Published October 7, 2000
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