Issue 33, 2021
From the journal:

Chemical Communications

Green-light induced cycloadditions†

Philipp W. Kamm,abc   James P. Blinco, ORCID logo *ab   Andreas-Neil Unterreiner ORCID logo *c  and  Christopher Barner-Kowollik ORCID logo *ab  

* Corresponding authors

a Centre for Materials Science, Queensland University of Technology (QUT), 2 George Street, Brisbane, QLD 4000, Australia
E-mail: j.blinco@qut.edu.au, christopher.barnerkowollik@qut.edu.au

b School of Chemistry and Physics, Queensland University of Technology (QUT), 2 George Street, Brisbane, QLD 4000, Australia

c Molecular Physical Chemistry Group, Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 2, Geb. 30.44, Karlsruhe 76131, Germany
E-mail: andreas.unterreiner@kit.edu

Abstract

We introduce a red-shifted tetrazole that is able to undergo efficient nitrile imine-mediated tetrazole–ene cycloaddition (NITEC) under blue and green light irradiation. We provide a detailed wavelength-dependent reactivity map, and employ a number of LEDs for high-conversion small molecule and polymer end-group modification.

Graphical abstract: Green-light induced cycloadditions

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Article information

DOI
https://doi.org/10.1039/D1CC00340B
Article type
Communication
Submitted
20 Jan 2021
Accepted
17 Mar 2021
First published
17 Mar 2021
This article is Open Access
Creative Commons BY license

Chem. Commun., 2021,57, 3991-3994

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Green-light induced cycloadditions

P. W. Kamm, J. P. Blinco, A. Unterreiner and C. Barner-Kowollik, Chem. Commun., 2021, 57, 3991 DOI: 10.1039/D1CC00340B

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