Issue 42, 2013

Synthesis and recognition studies with a ditopic, photoswitchable deep cavitand

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

Supplementary files

Article information

Article type
Communication
Submitted
21 Feb 2013
Accepted
20 Mar 2013
First published
21 Mar 2013

Chem. Commun., 2013,49, 4842-4844

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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