Cargando…
Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
Strongly fluorescence-emitting oligofluoranthene (OFA) nanorods are readily synthesized by a direct template-free chemical oxidative oligomerization of fluoranthene in nitromethane containing ferric chloride as an oxidant. The OFAs likely consist of five fluoranthene units containing cyclic pentamer...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951197/ https://www.ncbi.nlm.nih.gov/pubmed/29861955 http://dx.doi.org/10.1039/c5sc03041b |
_version_ | 1783322990670249984 |
---|---|
author | Li, Xin-Gui Liao, Yaozu Huang, Mei-Rong Kaner, Richard B. |
author_facet | Li, Xin-Gui Liao, Yaozu Huang, Mei-Rong Kaner, Richard B. |
author_sort | Li, Xin-Gui |
collection | PubMed |
description | Strongly fluorescence-emitting oligofluoranthene (OFA) nanorods are readily synthesized by a direct template-free chemical oxidative oligomerization of fluoranthene in nitromethane containing ferric chloride as an oxidant. The OFAs likely consist of five fluoranthene units containing cyclic pentamers with crystalline order and tunable electrical conductivity across 12 orders of magnitude. The OFA nanorods are heat-resistant materials and efficient precursors for macroporous carbon materials with high carbon yield in argon at 1100 °C. In particular, the optimal ring-like pentamer shows 12.2 times stronger cyan fluorescence-emission than recognized highly fluorescent fluoranthene under the same conditions, which makes the OFAs into ideal strong fluorescent emitters, tunable conductors, and high carbon-yield precursors for the preparation of sensors and carbon materials. These findings demonstrate an advance in the direct synthesis of oligomers from fused-ring aromatic hydrocarbons and provide a potential direction to optimize the synthesis and functionalities of wholly aromatic nanomaterials. |
format | Online Article Text |
id | pubmed-5951197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-59511972018-06-01 Efficient synthesis of oligofluoranthene nanorods with tunable functionalities Li, Xin-Gui Liao, Yaozu Huang, Mei-Rong Kaner, Richard B. Chem Sci Chemistry Strongly fluorescence-emitting oligofluoranthene (OFA) nanorods are readily synthesized by a direct template-free chemical oxidative oligomerization of fluoranthene in nitromethane containing ferric chloride as an oxidant. The OFAs likely consist of five fluoranthene units containing cyclic pentamers with crystalline order and tunable electrical conductivity across 12 orders of magnitude. The OFA nanorods are heat-resistant materials and efficient precursors for macroporous carbon materials with high carbon yield in argon at 1100 °C. In particular, the optimal ring-like pentamer shows 12.2 times stronger cyan fluorescence-emission than recognized highly fluorescent fluoranthene under the same conditions, which makes the OFAs into ideal strong fluorescent emitters, tunable conductors, and high carbon-yield precursors for the preparation of sensors and carbon materials. These findings demonstrate an advance in the direct synthesis of oligomers from fused-ring aromatic hydrocarbons and provide a potential direction to optimize the synthesis and functionalities of wholly aromatic nanomaterials. Royal Society of Chemistry 2015-12-01 2015-09-17 /pmc/articles/PMC5951197/ /pubmed/29861955 http://dx.doi.org/10.1039/c5sc03041b Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Li, Xin-Gui Liao, Yaozu Huang, Mei-Rong Kaner, Richard B. Efficient synthesis of oligofluoranthene nanorods with tunable functionalities |
title | Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
|
title_full | Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
|
title_fullStr | Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
|
title_full_unstemmed | Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
|
title_short | Efficient synthesis of oligofluoranthene nanorods with tunable functionalities
|
title_sort | efficient synthesis of oligofluoranthene nanorods with tunable functionalities |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951197/ https://www.ncbi.nlm.nih.gov/pubmed/29861955 http://dx.doi.org/10.1039/c5sc03041b |
work_keys_str_mv | AT lixingui efficientsynthesisofoligofluoranthenenanorodswithtunablefunctionalities AT liaoyaozu efficientsynthesisofoligofluoranthenenanorodswithtunablefunctionalities AT huangmeirong efficientsynthesisofoligofluoranthenenanorodswithtunablefunctionalities AT kanerrichardb efficientsynthesisofoligofluoranthenenanorodswithtunablefunctionalities |