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 a...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2018-12-01
|
| Series: | Molecules |
| Subjects: | |
| Online Access: | http://www.mdpi.com/1420-3049/24/1/118 |
| _version_ | 1818402381217398784 |
|---|---|
| author | Amber D. Senese Wesley A. Chalifoux |
| author_facet | Amber D. Senese Wesley A. Chalifoux |
| author_sort | Amber D. Senese |
| collection | DOAJ |
| 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. |
| first_indexed | 2024-12-14T08:07:27Z |
| format | Article |
| id | doaj.art-ef85c473832c4fbab01e528ad49bf9c4 |
| institution | Directory Open Access Journal |
| issn | 1420-3049 |
| language | English |
| last_indexed | 2024-12-14T08:07:27Z |
| publishDate | 2018-12-01 |
| publisher | MDPI AG |
| record_format | Article |
| series | Molecules |
| spelling | doaj.art-ef85c473832c4fbab01e528ad49bf9c42022-12-21T23:10:08ZengMDPI AGMolecules1420-30492018-12-0124111810.3390/molecules24010118molecules24010118Nanographene and Graphene Nanoribbon Synthesis via Alkyne BenzannulationsAmber D. Senese0Wesley A. Chalifoux1Department of Chemistry, University of Nevada, Reno, 1664 N. Virginia St., Reno, NV 89557, USADepartment of Chemistry, University of Nevada, Reno, 1664 N. Virginia St., Reno, NV 89557, USAThe 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.http://www.mdpi.com/1420-3049/24/1/118alkynebenzannulationnanographenepolycyclic aromatic hydrocarbongraphene nanoribbon |
| spellingShingle | Amber D. Senese Wesley A. Chalifoux Nanographene and Graphene Nanoribbon Synthesis via Alkyne Benzannulations Molecules alkyne benzannulation nanographene polycyclic aromatic hydrocarbon graphene nanoribbon |
| 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 | alkyne benzannulation nanographene polycyclic aromatic hydrocarbon graphene nanoribbon |
| url | http://www.mdpi.com/1420-3049/24/1/118 |
| work_keys_str_mv | AT amberdsenese nanographeneandgraphenenanoribbonsynthesisviaalkynebenzannulations AT wesleyachalifoux nanographeneandgraphenenanoribbonsynthesisviaalkynebenzannulations |