Issue 5, 2014

Deprotonation induced formation of Möbius aromatic [32]heptaphyrins

Abstract

Upon treatment with tetrabutylammonium fluoride (TBAF), [32]heptaphyrins 1 and 2 underwent conformational changes to form Möbius aromatic species, as indicated by the appearance of sharp and intense B-like bands and distinct Q-like bands, long-lived S1-states, and relatively large TPA cross-section values. Hence, deprotonation has been shown to be an additional effective means to induce the formation of Möbius aromatic expanded porphyrins.

Graphical abstract: Deprotonation induced formation of Möbius aromatic [32]heptaphyrins

Supplementary files

Article information

Article type
Communication
Submitted
15 Oct 2013
Accepted
06 Nov 2013
First published
07 Nov 2013

Chem. Commun., 2014,50, 548-550

Deprotonation induced formation of Möbius aromatic [32]heptaphyrins

W. Cha, T. Yoneda, S. Lee, J. M. Lim, A. Osuka and D. Kim, Chem. Commun., 2014, 50, 548 DOI: 10.1039/C3CC47908K

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