Issue 19, 2020

Keto–enol tautomerization drives the self-assembly of leucoquinizarin on Au(111)

Abstract

The self-assembly of leucoquinizarin molecules on Au(111) surfaces is shown to be characterized by the molecules mostly being in their keto–enolic tautomeric form, with evidence of their temporary switching to other tautomeric forms. This reveals a metastable chemistry of the assembled molecules, to be considered for their possible employment in the formation of more complex hetero-organic interfaces.

Graphical abstract: Keto–enol tautomerization drives the self-assembly of leucoquinizarin on Au(111)

Supplementary files

Article information

Article type
Communication
Submitted
22 Dec 2019
Accepted
06 Feb 2020
First published
06 Feb 2020
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2020,56, 2833-2836

Keto–enol tautomerization drives the self-assembly of leucoquinizarin on Au(111)

R. Costantini, L. Colazzo, L. Batini, M. Stredansky, M. S. G. Mohammed, S. Achilli, L. Floreano, G. Fratesi, D. G. de Oteyza and A. Cossaro, Chem. Commun., 2020, 56, 2833 DOI: 10.1039/C9CC09915H

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