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Issue 42, 2013
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Synthesis and recognition studies with a ditopic, photoswitchable deep cavitand

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Abstract

We describe the synthesis and photochemical behavior of open-ended container modules connected by a 4,4′-azobiphenyl spacer. Both trans and cis azo configurations of the host can be accessed and their binding of guest molecules was characterized by NMR methods.

Graphical abstract: Synthesis and recognition studies with a ditopic, photoswitchable deep cavitand

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Publication details

The article was received on 21 Feb 2013, accepted on 20 Mar 2013 and first published on 21 Mar 2013


Article type: Communication
DOI: 10.1039/C3CC41369A
Citation: Chem. Commun., 2013,49, 4842-4844
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    Synthesis and recognition studies with a ditopic, photoswitchable deep cavitand

    E. Busseron, J. Lux, M. Degardin and J. Rebek, Chem. Commun., 2013, 49, 4842
    DOI: 10.1039/C3CC41369A

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