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Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations
The extension of π-conjugation of polycyclic aromatic hydrocarbons (PAHs) via alkyne benzannulation reactions has become an increasingly utilized tool over the past few years. This short review will highlight recent work of alkyne benzannulations in the context of large nanographene as well as graph...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337508/ https://www.ncbi.nlm.nih.gov/pubmed/30598009 http://dx.doi.org/10.3390/molecules24010118 |
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author | Senese, Amber D. Chalifoux, Wesley A. |
author_facet | Senese, Amber D. Chalifoux, Wesley A. |
author_sort | Senese, Amber D. |
collection | PubMed |
description | The extension of π-conjugation of polycyclic aromatic hydrocarbons (PAHs) via alkyne benzannulation reactions has become an increasingly utilized tool over the past few years. This short review will highlight recent work of alkyne benzannulations in the context of large nanographene as well as graphene nanoribbon synthesis along with a brief discussion of the interesting physical properties these molecules display. |
format | Online Article Text |
id | pubmed-6337508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63375082019-01-25 Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations Senese, Amber D. Chalifoux, Wesley A. Molecules Review The extension of π-conjugation of polycyclic aromatic hydrocarbons (PAHs) via alkyne benzannulation reactions has become an increasingly utilized tool over the past few years. This short review will highlight recent work of alkyne benzannulations in the context of large nanographene as well as graphene nanoribbon synthesis along with a brief discussion of the interesting physical properties these molecules display. MDPI 2018-12-30 /pmc/articles/PMC6337508/ /pubmed/30598009 http://dx.doi.org/10.3390/molecules24010118 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Senese, Amber D. Chalifoux, Wesley A. Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title | Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title_full | Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title_fullStr | Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title_full_unstemmed | Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title_short | Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations |
title_sort | nanographene and graphene nanoribbon synthesis via alkyne benzannulations |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337508/ https://www.ncbi.nlm.nih.gov/pubmed/30598009 http://dx.doi.org/10.3390/molecules24010118 |
work_keys_str_mv | AT seneseamberd nanographeneandgraphenenanoribbonsynthesisviaalkynebenzannulations AT chalifouxwesleya nanographeneandgraphenenanoribbonsynthesisviaalkynebenzannulations |