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Two-Dimensional Self-Assembly Driven by Intermolecular Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111)
[Image: see text] The control of molecular structures at the nanoscale plays a critical role in the development of materials and applications. The adsorption of a polyheteroaromatic molecule with hydrogen bond donor and acceptor sites integrated in the conjugated structure itself, namely, benzodi-7-...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291637/ https://www.ncbi.nlm.nih.gov/pubmed/37377501 http://dx.doi.org/10.1021/acs.jpcc.3c01640 |
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author | Abad, José Martínez, José I. Gómez, Paula Más-Montoya, Miriam Rodríguez, Luis Cossaro, Albano Verdini, Alberto Floreano, Luca Martín-Gago, José A. Curiel, David Méndez, Javier |
author_facet | Abad, José Martínez, José I. Gómez, Paula Más-Montoya, Miriam Rodríguez, Luis Cossaro, Albano Verdini, Alberto Floreano, Luca Martín-Gago, José A. Curiel, David Méndez, Javier |
author_sort | Abad, José |
collection | PubMed |
description | [Image: see text] The control of molecular structures at the nanoscale plays a critical role in the development of materials and applications. The adsorption of a polyheteroaromatic molecule with hydrogen bond donor and acceptor sites integrated in the conjugated structure itself, namely, benzodi-7-azaindole (BDAI), has been studied on Au(111). Intermolecular hydrogen bonding determines the formation of highly organized linear structures where surface chirality, resulting from the 2D confinement of the centrosymmetric molecules, is observed. Moreover, the structural features of the BDAI molecule lead to the formation of two differentiated arrangements with extended brick-wall and herringbone packing. A comprehensive experimental study that combines scanning tunneling microscopy, high-resolution X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy, and density functional theory theoretical calculations has been performed to fully characterize the 2D hydrogen-bonded domains and the on-surface thermal stability of the physisorbed material. |
format | Online Article Text |
id | pubmed-10291637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102916372023-06-27 Two-Dimensional Self-Assembly Driven by Intermolecular Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) Abad, José Martínez, José I. Gómez, Paula Más-Montoya, Miriam Rodríguez, Luis Cossaro, Albano Verdini, Alberto Floreano, Luca Martín-Gago, José A. Curiel, David Méndez, Javier J Phys Chem C Nanomater Interfaces [Image: see text] The control of molecular structures at the nanoscale plays a critical role in the development of materials and applications. The adsorption of a polyheteroaromatic molecule with hydrogen bond donor and acceptor sites integrated in the conjugated structure itself, namely, benzodi-7-azaindole (BDAI), has been studied on Au(111). Intermolecular hydrogen bonding determines the formation of highly organized linear structures where surface chirality, resulting from the 2D confinement of the centrosymmetric molecules, is observed. Moreover, the structural features of the BDAI molecule lead to the formation of two differentiated arrangements with extended brick-wall and herringbone packing. A comprehensive experimental study that combines scanning tunneling microscopy, high-resolution X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy, and density functional theory theoretical calculations has been performed to fully characterize the 2D hydrogen-bonded domains and the on-surface thermal stability of the physisorbed material. American Chemical Society 2023-06-08 /pmc/articles/PMC10291637/ /pubmed/37377501 http://dx.doi.org/10.1021/acs.jpcc.3c01640 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Abad, José Martínez, José I. Gómez, Paula Más-Montoya, Miriam Rodríguez, Luis Cossaro, Albano Verdini, Alberto Floreano, Luca Martín-Gago, José A. Curiel, David Méndez, Javier Two-Dimensional Self-Assembly Driven by Intermolecular Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title | Two-Dimensional
Self-Assembly Driven by Intermolecular
Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title_full | Two-Dimensional
Self-Assembly Driven by Intermolecular
Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title_fullStr | Two-Dimensional
Self-Assembly Driven by Intermolecular
Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title_full_unstemmed | Two-Dimensional
Self-Assembly Driven by Intermolecular
Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title_short | Two-Dimensional
Self-Assembly Driven by Intermolecular
Hydrogen Bonding in Benzodi-7-azaindole Molecules on Au(111) |
title_sort | two-dimensional
self-assembly driven by intermolecular
hydrogen bonding in benzodi-7-azaindole molecules on au(111) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291637/ https://www.ncbi.nlm.nih.gov/pubmed/37377501 http://dx.doi.org/10.1021/acs.jpcc.3c01640 |
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