Direct growth of crystalline triazine-based graphdiyne using surface-assisted deprotection-polymerisation.
Journal
Chemical science
ISSN: 2041-6520
Titre abrégé: Chem Sci
Pays: England
ID NLM: 101545951
Informations de publication
Date de publication:
06 Oct 2021
06 Oct 2021
Historique:
received:
22
06
2021
accepted:
25
08
2021
entrez:
27
10
2021
pubmed:
28
10
2021
medline:
28
10
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 34703551
doi: 10.1039/d1sc03390e
pii: d1sc03390e
pmc: PMC8494036
doi:
Types de publication
Journal Article
Langues
eng
Pagination
12661-12666Informations de copyright
This journal is © The Royal Society of Chemistry.
Déclaration de conflit d'intérêts
There are no conflicts to declare.
Références
Chem Commun (Camb). 2011 Nov 21;47(43):11843-5
pubmed: 21952115
ACS Appl Mater Interfaces. 2017 Sep 6;9(35):29744-29752
pubmed: 28812362
Nano Lett. 2020 Oct 14;20(10):7333-7341
pubmed: 32881527
Adv Mater. 2017 May;29(18):
pubmed: 28251693
ACS Appl Mater Interfaces. 2019 Jan 23;11(3):2632-2637
pubmed: 29620348
Nanoscale. 2012 Aug 7;4(15):4587-93
pubmed: 22706782
Angew Chem Int Ed Engl. 2013 Apr 2;52(14):4024-8
pubmed: 23424176
J Org Chem. 2005 Jan 21;70(2):703-6
pubmed: 15651824
J Am Chem Soc. 2014 Sep 3;136(35):12194-200
pubmed: 25126670
Sci Adv. 2018 Jul 06;4(7):eaat6378
pubmed: 29984309
J Am Chem Soc. 2019 Jan 9;141(1):48-52
pubmed: 30569704
Chem Commun (Camb). 2017 Jul 13;53(57):8074-8077
pubmed: 28677693
Angew Chem Int Ed Engl. 2019 Jul 8;58(28):9394-9398
pubmed: 31070846
Adv Mater. 2017 Oct;29(40):
pubmed: 28859235
Macromol Rapid Commun. 2013 May 27;34(10):850-4
pubmed: 23512848
ChemSusChem. 2019 Jan 10;12(1):194-199
pubmed: 30335905
Angew Chem Int Ed Engl. 2014 Jul 14;53(29):7450-5
pubmed: 24838808
Acc Chem Res. 2015 Jul 21;48(7):2140-50
pubmed: 26156663
Nat Commun. 2019 Jul 19;10(1):3228
pubmed: 31324876
ACS Appl Mater Interfaces. 2019 Jan 23;11(3):2734-2739
pubmed: 29600713
Chem Commun (Camb). 2010 May 21;46(19):3256-8
pubmed: 20442882
Phys Chem Chem Phys. 2014 Jun 21;16(23):11303-9
pubmed: 24789090
Chem Soc Rev. 2019 Feb 4;48(3):908-936
pubmed: 30608070
Chem Commun (Camb). 2019 Apr 4;55(29):4178-4181
pubmed: 30888385
J Am Chem Soc. 2017 May 24;139(20):7012-7019
pubmed: 28466640
Chemistry. 2016 May 17;22(21):7179-83
pubmed: 27080951