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

Chem Commun (Camb). 2020 Mar 5;56(19):2833-2836. doi: 10.1039/c9cc09915h.

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.