Issue 62, 2018
From the journal:

Chemical Communications

A two-step approach to a glycoazobenzene macrocycle with remarkable photoswitchable features†

Julia Hain ORCID logo a  and  Guillaume Despras ORCID logo *a  

* Corresponding authors

a Otto Diels Institute of Organic Chemistry Christiana Albertina University of Kiel Otto-Hahn-Platz 3/4, 24118 Kiel, Germany
E-mail: gdespras@oc.uni-kiel.de

Abstract

A combination of the Mitsunobu reaction and Glaser coupling was used to achieve a new glycoazobenzene macrocycle. This photosensitive macrocycle can be efficiently and reversibly switched between two stable conformational isomers, which are characterized with photoswitchable shape, chiroptical and solubility behaviour.

Graphical abstract: A two-step approach to a glycoazobenzene macrocycle with remarkable photoswitchable features

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Article information

DOI
https://doi.org/10.1039/C8CC03724H
Article type
Communication
Submitted
08 May 2018
Accepted
31 May 2018
First published
31 May 2018

Chem. Commun., 2018,54, 8563-8566

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A two-step approach to a glycoazobenzene macrocycle with remarkable photoswitchable features

J. Hain and G. Despras, Chem. Commun., 2018, 54, 8563 DOI: 10.1039/C8CC03724H

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