Logo del repository
  1. Home
 
Opzioni

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

Costantini, Roberto
•
Colazzo, Luciano
•
Batini, Laura
altro
Cossaro, Albano
2020
  • journal article

Periodico
CHEMICAL COMMUNICATIONS
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.
DOI
10.1039/C9CC09915H
WOS
WOS:000519216400031
Archivio
http://hdl.handle.net/11368/2962051
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85081078146
Diritti
open access
license:creative commons
license:creative commons
license uri:http://creativecommons.org/licenses/by/4.0/
license uri:http://creativecommons.org/licenses/by/4.0/
FVG url
https://arts.units.it/bitstream/11368/2962051/2/c9cc09915h.pdf
Soggetti
  • Self-assembly

  • Leucoquinizarin

  • Keto-enol tautomerism...

Scopus© citazioni
1
Data di acquisizione
Jun 14, 2022
Vedi dettagli
Web of Science© citazioni
1
Data di acquisizione
Mar 27, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
Vedi dettagli
google-scholar
Get Involved!
  • Source Code
  • Documentation
  • Slack Channel
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your nstitution's web identity.

Need professional help?

The original creators of DSpace-CRIS at 4Science can take your project to the next level, get in touch!

Realizzato con Software DSpace-CRIS - Estensione mantenuta e ottimizzata da 4Science

  • Impostazioni dei cookie
  • Informativa sulla privacy
  • Accordo con l'utente finale
  • Invia il tuo Feedback