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Issue 3, 2009
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Upper-rim alternately tethered α-cyclodextrin molecular receptors: synthesis, metal complexation and interfacial behavior

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Abstract

Three novel α-cyclodextrin tripods bearing three ureido-bipyridyl tethers symmetrically distributed on their upper rim in the A,C,E positions and alternated with hydroxyl, acetyl or lauryl moieties were prepared by the tandem Staudinger–Aza–Wittig alias“phosphine imide” strategy. The functionalisations on the cyclodextrin upper rim allowed a fine-tuning of the metal complexation and amphiphilic properties.

Graphical abstract: Upper-rim alternately tethered α-cyclodextrin molecular receptors: synthesis, metal complexation and interfacial behavior

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Publication details

The article was received on 30 May 2008, accepted on 17 Oct 2008 and first published on 26 Nov 2008


Article type: Paper
DOI: 10.1039/B809151J
Citation: New J. Chem., 2009,33, 554-560
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    Upper-rim alternately tethered α-cyclodextrin molecular receptors: synthesis, metal complexation and interfacial behavior

    S. Menuel, Y. Corvis, E. Rogalska and A. Marsura, New J. Chem., 2009, 33, 554
    DOI: 10.1039/B809151J

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