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Extreme red shifted SERS nanotags
Surfaced enhanced Raman scattering (SERS) nanotags operating with 1280 nm excitation were constructed from reporter molecules selected from a library of 14 chalcogenopyrylium dyes containing phenyl, 2-thienyl, and 2-selenophenyl substituents and a surface of hollow gold nanoshells (HGNs). These 1280...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645778/ https://www.ncbi.nlm.nih.gov/pubmed/29308144 http://dx.doi.org/10.1039/c4sc03917c |
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author | Bedics, Matthew A. Kearns, Hayleigh Cox, Jordan M. Mabbott, Sam Ali, Fatima Shand, Neil C. Faulds, Karen Benedict, Jason B. Graham, Duncan Detty, Michael R. |
author_facet | Bedics, Matthew A. Kearns, Hayleigh Cox, Jordan M. Mabbott, Sam Ali, Fatima Shand, Neil C. Faulds, Karen Benedict, Jason B. Graham, Duncan Detty, Michael R. |
author_sort | Bedics, Matthew A. |
collection | PubMed |
description | Surfaced enhanced Raman scattering (SERS) nanotags operating with 1280 nm excitation were constructed from reporter molecules selected from a library of 14 chalcogenopyrylium dyes containing phenyl, 2-thienyl, and 2-selenophenyl substituents and a surface of hollow gold nanoshells (HGNs). These 1280 SERS nanotags are unique as they have multiple chalcogen atoms available which allow them to adsorb strongly onto the gold surface of the HGN thus producing exceptional SERS signals at this long excitation wavelength. Picomolar limits of detection (LOD) were observed and individual reporters of the library were identified by principal component analysis and classified according to their unique structure and SERS spectra. |
format | Online Article Text |
id | pubmed-5645778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56457782018-01-05 Extreme red shifted SERS nanotags Bedics, Matthew A. Kearns, Hayleigh Cox, Jordan M. Mabbott, Sam Ali, Fatima Shand, Neil C. Faulds, Karen Benedict, Jason B. Graham, Duncan Detty, Michael R. Chem Sci Chemistry Surfaced enhanced Raman scattering (SERS) nanotags operating with 1280 nm excitation were constructed from reporter molecules selected from a library of 14 chalcogenopyrylium dyes containing phenyl, 2-thienyl, and 2-selenophenyl substituents and a surface of hollow gold nanoshells (HGNs). These 1280 SERS nanotags are unique as they have multiple chalcogen atoms available which allow them to adsorb strongly onto the gold surface of the HGN thus producing exceptional SERS signals at this long excitation wavelength. Picomolar limits of detection (LOD) were observed and individual reporters of the library were identified by principal component analysis and classified according to their unique structure and SERS spectra. Royal Society of Chemistry 2015-04-01 2015-01-21 /pmc/articles/PMC5645778/ /pubmed/29308144 http://dx.doi.org/10.1039/c4sc03917c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Bedics, Matthew A. Kearns, Hayleigh Cox, Jordan M. Mabbott, Sam Ali, Fatima Shand, Neil C. Faulds, Karen Benedict, Jason B. Graham, Duncan Detty, Michael R. Extreme red shifted SERS nanotags |
title | Extreme red shifted SERS nanotags
|
title_full | Extreme red shifted SERS nanotags
|
title_fullStr | Extreme red shifted SERS nanotags
|
title_full_unstemmed | Extreme red shifted SERS nanotags
|
title_short | Extreme red shifted SERS nanotags
|
title_sort | extreme red shifted sers nanotags |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645778/ https://www.ncbi.nlm.nih.gov/pubmed/29308144 http://dx.doi.org/10.1039/c4sc03917c |
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