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From starphenes to non-benzenoid linear conjugated polymers by substrate templating

Combining on-surface synthetic methods with the power of scanning tunneling microscopy to characterize novel materials at the single molecule level, we show how to steer the reactivity of one anthracene-based precursor towards different product nanostructures. Whereas using a Au(111) surface with th...

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Autores principales: Mohammed, Mohammed S. G., Lawrence, James, García, Fátima, Brandimarte, Pedro, Berdonces-Layunta, Alejandro, Pérez, Dolores, Sánchez-Portal, Daniel, Peña, Diego, de Oteyza, Dimas G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419161/
https://www.ncbi.nlm.nih.gov/pubmed/36133758
http://dx.doi.org/10.1039/d1na00126d
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author Mohammed, Mohammed S. G.
Lawrence, James
García, Fátima
Brandimarte, Pedro
Berdonces-Layunta, Alejandro
Pérez, Dolores
Sánchez-Portal, Daniel
Peña, Diego
de Oteyza, Dimas G.
author_facet Mohammed, Mohammed S. G.
Lawrence, James
García, Fátima
Brandimarte, Pedro
Berdonces-Layunta, Alejandro
Pérez, Dolores
Sánchez-Portal, Daniel
Peña, Diego
de Oteyza, Dimas G.
author_sort Mohammed, Mohammed S. G.
collection PubMed
description Combining on-surface synthetic methods with the power of scanning tunneling microscopy to characterize novel materials at the single molecule level, we show how to steer the reactivity of one anthracene-based precursor towards different product nanostructures. Whereas using a Au(111) surface with three-fold symmetry results in the dominant formation of a starphene derivative, the two-fold symmetry of a reconstructed Au(110) surface allows the selective growth of non-benzenoid linear conjugated polymers. We further assess the electronic properties of each of the observed product structures via tunneling spectroscopy and DFT calculations, altogether advancing the synthesis and characterization of molecular structures of notable scientific interest that have been only scarcely investigated to date, as applies both to starphenes and to non-benzenoid conjugated polymers.
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spelling pubmed-94191612022-09-20 From starphenes to non-benzenoid linear conjugated polymers by substrate templating Mohammed, Mohammed S. G. Lawrence, James García, Fátima Brandimarte, Pedro Berdonces-Layunta, Alejandro Pérez, Dolores Sánchez-Portal, Daniel Peña, Diego de Oteyza, Dimas G. Nanoscale Adv Chemistry Combining on-surface synthetic methods with the power of scanning tunneling microscopy to characterize novel materials at the single molecule level, we show how to steer the reactivity of one anthracene-based precursor towards different product nanostructures. Whereas using a Au(111) surface with three-fold symmetry results in the dominant formation of a starphene derivative, the two-fold symmetry of a reconstructed Au(110) surface allows the selective growth of non-benzenoid linear conjugated polymers. We further assess the electronic properties of each of the observed product structures via tunneling spectroscopy and DFT calculations, altogether advancing the synthesis and characterization of molecular structures of notable scientific interest that have been only scarcely investigated to date, as applies both to starphenes and to non-benzenoid conjugated polymers. RSC 2021-03-08 /pmc/articles/PMC9419161/ /pubmed/36133758 http://dx.doi.org/10.1039/d1na00126d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mohammed, Mohammed S. G.
Lawrence, James
García, Fátima
Brandimarte, Pedro
Berdonces-Layunta, Alejandro
Pérez, Dolores
Sánchez-Portal, Daniel
Peña, Diego
de Oteyza, Dimas G.
From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title_full From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title_fullStr From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title_full_unstemmed From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title_short From starphenes to non-benzenoid linear conjugated polymers by substrate templating
title_sort from starphenes to non-benzenoid linear conjugated polymers by substrate templating
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419161/
https://www.ncbi.nlm.nih.gov/pubmed/36133758
http://dx.doi.org/10.1039/d1na00126d
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