On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains

Strain-induced on-surface transformations provide an appealing route to steer the selectivity towards desired products. Here, we demonstrate the selective on-surface synthesis of extended all-<i>trans</i> poly(2,6-pyridine) chains on Au(111). By combining high-resolution scanning tunneli...

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Main Authors: Laerte L. Patera, Josef Amler, Jascha Repp
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Chemistry
Subjects:
Online Access:https://www.mdpi.com/2624-8549/4/1/9
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author Laerte L. Patera
Josef Amler
Jascha Repp
author_facet Laerte L. Patera
Josef Amler
Jascha Repp
author_sort Laerte L. Patera
collection DOAJ
description Strain-induced on-surface transformations provide an appealing route to steer the selectivity towards desired products. Here, we demonstrate the selective on-surface synthesis of extended all-<i>trans</i> poly(2,6-pyridine) chains on Au(111). By combining high-resolution scanning tunneling and atomic force microscopy, we revealed the detailed chemical structure of the reaction products. Density functional theory calculations indicate that the synthesis of extended covalent structures is energetically favored over the formation of macrocycles, due to the minimization of internal strain. Our results consolidate the exploitation of internal strain relief as a driving force to promote selective on-surface reactions.
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spelling doaj.art-a06e672ac2e94b3eae86176f8e4d87602023-11-24T00:45:36ZengMDPI AGChemistry2624-85492022-02-014111211710.3390/chemistry4010009On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear ChainsLaerte L. Patera0Josef Amler1Jascha Repp2Institute of Experimental and Applied Physics, University of Regensburg, 93053 Regensburg, GermanyInstitute of Experimental and Applied Physics, University of Regensburg, 93053 Regensburg, GermanyInstitute of Experimental and Applied Physics, University of Regensburg, 93053 Regensburg, GermanyStrain-induced on-surface transformations provide an appealing route to steer the selectivity towards desired products. Here, we demonstrate the selective on-surface synthesis of extended all-<i>trans</i> poly(2,6-pyridine) chains on Au(111). By combining high-resolution scanning tunneling and atomic force microscopy, we revealed the detailed chemical structure of the reaction products. Density functional theory calculations indicate that the synthesis of extended covalent structures is energetically favored over the formation of macrocycles, due to the minimization of internal strain. Our results consolidate the exploitation of internal strain relief as a driving force to promote selective on-surface reactions.https://www.mdpi.com/2624-8549/4/1/9on-surface synthesisAFMSTMDFT calculations
spellingShingle Laerte L. Patera
Josef Amler
Jascha Repp
On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
Chemistry
on-surface synthesis
AFM
STM
DFT calculations
title On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
title_full On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
title_fullStr On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
title_full_unstemmed On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
title_short On-Surface Synthesis of Polypyridine: Strain Enforces Extended Linear Chains
title_sort on surface synthesis of polypyridine strain enforces extended linear chains
topic on-surface synthesis
AFM
STM
DFT calculations
url https://www.mdpi.com/2624-8549/4/1/9
work_keys_str_mv AT laertelpatera onsurfacesynthesisofpolypyridinestrainenforcesextendedlinearchains
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