Issue 87, 2015

Towards the tailored design of benzotriazinyl-based organic radicals displaying a spin transition

Abstract

The mechanism of the phase transition of 1-phenyl-3-trifluoromethyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl (1), the first reported triazinyl radical to present such a feature, is unveiled. In so doing, we identify the key ingredients that are crucial to enable the phase transition in this family of radicals, and how those can be exploited by a rational design of the spin-carrying units.

Graphical abstract: Towards the tailored design of benzotriazinyl-based organic radicals displaying a spin transition

Supplementary files

Article information

Article type
Communication
Submitted
27 Jul 2015
Accepted
03 Sep 2015
First published
03 Sep 2015

Chem. Commun., 2015,51, 15776-15779

Towards the tailored design of benzotriazinyl-based organic radicals displaying a spin transition

M. Fumanal, S. Vela, J. J. Novoa and J. Ribas-Arino, Chem. Commun., 2015, 51, 15776 DOI: 10.1039/C5CC06288H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements