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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...

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Autores principales: Kulkarni, Ranjit, Huang, Jieyang, Trunk, Matthias, Burmeister, David, Amsalem, Patrick, Müller, Johannes, Martin, Andréa, Koch, Norbert, Kass, Dustin, Bojdys, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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.
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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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