Synthesis of radiaannulene oligomers to model the elusive carbon allotrope 6,6,12-graphyne-Reference-Cited by-同舟云学术

Synthesis of radiaannulene oligomers to model the elusive carbon allotrope 6,6,12-graphyne

Published:2019-08-16 Issue:1 Volume:10 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Kilde Martin Drøhse,Murray Adrian H.^ORCID,Andersen Cecilie Lindholm,Storm Freja Eilsø^ORCID,Schmidt Katrin,Kadziola Anders,Mikkelsen Kurt V.,Hampel Frank,Hammerich Ole^ORCID,Tykwinski Rik R.^ORCID,Nielsen Mogens Brøndsted

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-019-11700-0.pdf

Reference39 articles.

1. Falcao, E. H. L. & Wudl, F. Carbon allotropes: beyond graphite and diamond. J. Chem. Technol. Biotechnol. 82, 524–531 (2007).

2. Hirsch, A. The era of carbon allotropes. Nat. Mat. 9, 868–871 (2010).

3. Geim, A. K. & Novoselov, K. S. The rise of graphene. Nat. Mat. 6, 183–191 (2007).

4. Cai, J. et al. Atomically precise bottom-up fabrication of graphene nanoribbons. Nature 466, 470–473 (2010).

5. Merino-Díez, N. et al. Width-dependent band gap in armchair graphene nanoribbons reveals Fermi level pinning on Au(111). ACS Nano 11, 11661–11668 (2017).

Cited by 35 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sr-centered monocyclic carbon ring Sr@C14: A new stable cluster;Journal of Molecular Graphics and Modelling;2024-05

2. Unlocking Diverse π-Bond Enrichment Frameworks by the Synthesis and Conversion of Boronated Phenyldiethynylethylenes;Journal of the American Chemical Society;2024-03-27

3. High-order harmonic signal of bond-length-variable C18 and its application in optical logic gates;Physical Review A;2024-02-22

4. Hybrid scheme of DFT and machine learning to accelerate the design of graphyne nanoribbons as electrocatalysts for the ORR and HER;Fuel;2024-02

5. Multi-redox indenofluorene chromophores incorporating dithiafulvene donor and ene/enediyne acceptor units;Beilstein Journal of Organic Chemistry;2024-01-15