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Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation
Graphdiyne polymers have interesting electronic properties due to their π-conjugated structure and modular composition. Most of the known synthetic pathways for graphdiyne polymers yield amorphous solids because the irreversible formation of carbon–carbon bonds proceeds under kinetic control and bec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494036/ https://www.ncbi.nlm.nih.gov/pubmed/34703551 http://dx.doi.org/10.1039/d1sc03390e |
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author | Kulkarni, Ranjit Huang, Jieyang Trunk, Matthias Burmeister, David Amsalem, Patrick Müller, Johannes Martin, Andréa Koch, Norbert Kass, Dustin Bojdys, Michael J. |
author_facet | Kulkarni, Ranjit Huang, Jieyang Trunk, Matthias Burmeister, David Amsalem, Patrick Müller, Johannes Martin, Andréa Koch, Norbert Kass, Dustin Bojdys, Michael J. |
author_sort | Kulkarni, Ranjit |
collection | PubMed |
description | Graphdiyne polymers have interesting electronic properties due to their π-conjugated structure and modular composition. Most of the known synthetic pathways for graphdiyne polymers yield amorphous solids because the irreversible formation of carbon–carbon bonds proceeds under kinetic control and because of defects introduced by the inherent chemical lability of terminal alkyne bonds in the monomers. Here, we present a one-pot surface-assisted deprotection/polymerisation protocol for the synthesis of crystalline graphdiynes over a copper surface starting with stable trimethylsilylated alkyne monomers. In comparison to conventional polymerisation protocols, our method yields large-area crystalline thin graphdiyne films and, at the same time, minimises detrimental effects on the monomers like oxidation or cyclotrimerisation side reactions typically associated with terminal alkynes. A detailed study of the reaction mechanism reveals that the deprotection and polymerisation of the monomer is promoted by Cu(ii) oxide/hydroxide species on the as-received copper surface. These findings pave the way for the scalable synthesis of crystalline graphdiyne-based materials as cohesive thin films. |
format | Online Article Text |
id | pubmed-8494036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-84940362021-10-25 Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation Kulkarni, Ranjit Huang, Jieyang Trunk, Matthias Burmeister, David Amsalem, Patrick Müller, Johannes Martin, Andréa Koch, Norbert Kass, Dustin Bojdys, Michael J. Chem Sci Chemistry Graphdiyne polymers have interesting electronic properties due to their π-conjugated structure and modular composition. Most of the known synthetic pathways for graphdiyne polymers yield amorphous solids because the irreversible formation of carbon–carbon bonds proceeds under kinetic control and because of defects introduced by the inherent chemical lability of terminal alkyne bonds in the monomers. Here, we present a one-pot surface-assisted deprotection/polymerisation protocol for the synthesis of crystalline graphdiynes over a copper surface starting with stable trimethylsilylated alkyne monomers. In comparison to conventional polymerisation protocols, our method yields large-area crystalline thin graphdiyne films and, at the same time, minimises detrimental effects on the monomers like oxidation or cyclotrimerisation side reactions typically associated with terminal alkynes. A detailed study of the reaction mechanism reveals that the deprotection and polymerisation of the monomer is promoted by Cu(ii) oxide/hydroxide species on the as-received copper surface. These findings pave the way for the scalable synthesis of crystalline graphdiyne-based materials as cohesive thin films. The Royal Society of Chemistry 2021-08-26 /pmc/articles/PMC8494036/ /pubmed/34703551 http://dx.doi.org/10.1039/d1sc03390e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Kulkarni, Ranjit Huang, Jieyang Trunk, Matthias Burmeister, David Amsalem, Patrick Müller, Johannes Martin, Andréa Koch, Norbert Kass, Dustin Bojdys, Michael J. Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title | Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title_full | Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title_fullStr | Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title_full_unstemmed | Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title_short | Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
title_sort | direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection–polymerisation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494036/ https://www.ncbi.nlm.nih.gov/pubmed/34703551 http://dx.doi.org/10.1039/d1sc03390e |
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