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Intramolecular Coupling of Terminal Alkynes by Atom Manipulation

Glaser‐like coupling of terminal alkynes by thermal activation is extensively used in on‐surface chemistry. Here we demonstrate an intramolecular version of this reaction performed by atom manipulation. We used voltage pulses from the tip to trigger a Glaser‐like coupling between terminal alkyne car...

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Autores principales: Albrecht, Florian, Rey, Dulce, Fatayer, Shadi, Schulz, Fabian, Pérez, Dolores, Peña, Diego, Gross, Leo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756451/
https://www.ncbi.nlm.nih.gov/pubmed/32845044
http://dx.doi.org/10.1002/anie.202009200
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author Albrecht, Florian
Rey, Dulce
Fatayer, Shadi
Schulz, Fabian
Pérez, Dolores
Peña, Diego
Gross, Leo
author_facet Albrecht, Florian
Rey, Dulce
Fatayer, Shadi
Schulz, Fabian
Pérez, Dolores
Peña, Diego
Gross, Leo
author_sort Albrecht, Florian
collection PubMed
description Glaser‐like coupling of terminal alkynes by thermal activation is extensively used in on‐surface chemistry. Here we demonstrate an intramolecular version of this reaction performed by atom manipulation. We used voltage pulses from the tip to trigger a Glaser‐like coupling between terminal alkyne carbons within a custom‐synthesized precursor molecule adsorbed on bilayer NaCl on Cu(111). Different conformations of the precursor molecule and the product were characterized by molecular structure elucidation with atomic force microscopy and orbital density mapping with scanning tunneling microscopy, accompanied by density functional theory calculations. We revealed partially dehydrogenated intermediates, providing insight into the reaction pathway.
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spelling pubmed-77564512020-12-28 Intramolecular Coupling of Terminal Alkynes by Atom Manipulation Albrecht, Florian Rey, Dulce Fatayer, Shadi Schulz, Fabian Pérez, Dolores Peña, Diego Gross, Leo Angew Chem Int Ed Engl Communications Glaser‐like coupling of terminal alkynes by thermal activation is extensively used in on‐surface chemistry. Here we demonstrate an intramolecular version of this reaction performed by atom manipulation. We used voltage pulses from the tip to trigger a Glaser‐like coupling between terminal alkyne carbons within a custom‐synthesized precursor molecule adsorbed on bilayer NaCl on Cu(111). Different conformations of the precursor molecule and the product were characterized by molecular structure elucidation with atomic force microscopy and orbital density mapping with scanning tunneling microscopy, accompanied by density functional theory calculations. We revealed partially dehydrogenated intermediates, providing insight into the reaction pathway. John Wiley and Sons Inc. 2020-10-13 2020-12-14 /pmc/articles/PMC7756451/ /pubmed/32845044 http://dx.doi.org/10.1002/anie.202009200 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Albrecht, Florian
Rey, Dulce
Fatayer, Shadi
Schulz, Fabian
Pérez, Dolores
Peña, Diego
Gross, Leo
Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title_full Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title_fullStr Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title_full_unstemmed Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title_short Intramolecular Coupling of Terminal Alkynes by Atom Manipulation
title_sort intramolecular coupling of terminal alkynes by atom manipulation
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756451/
https://www.ncbi.nlm.nih.gov/pubmed/32845044
http://dx.doi.org/10.1002/anie.202009200
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