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Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
Amino-substituted maleimides form a new class of highly emissive compounds, with large Stokes shifts (>100 nm) and high quantum yields (up to ∼60%). Emission is responsive to the maleimide's environment with both a red-shift, and quenching, observed in protic polar solvents. Aminomaleimides...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540011/ https://www.ncbi.nlm.nih.gov/pubmed/25985397 http://dx.doi.org/10.1039/c5cc02908b |
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author | Mabire, Anne B. Robin, Mathew P. Quan, Wen-Dong Willcock, Helen Stavros, Vasilios G. O'Reilly, Rachel K. |
author_facet | Mabire, Anne B. Robin, Mathew P. Quan, Wen-Dong Willcock, Helen Stavros, Vasilios G. O'Reilly, Rachel K. |
author_sort | Mabire, Anne B. |
collection | PubMed |
description | Amino-substituted maleimides form a new class of highly emissive compounds, with large Stokes shifts (>100 nm) and high quantum yields (up to ∼60%). Emission is responsive to the maleimide's environment with both a red-shift, and quenching, observed in protic polar solvents. Aminomaleimides are easily functionalised, providing a versatile fluorescent probe. |
format | Online Article Text |
id | pubmed-4540011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-45400112015-09-09 Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission Mabire, Anne B. Robin, Mathew P. Quan, Wen-Dong Willcock, Helen Stavros, Vasilios G. O'Reilly, Rachel K. Chem Commun (Camb) Chemistry Amino-substituted maleimides form a new class of highly emissive compounds, with large Stokes shifts (>100 nm) and high quantum yields (up to ∼60%). Emission is responsive to the maleimide's environment with both a red-shift, and quenching, observed in protic polar solvents. Aminomaleimides are easily functionalised, providing a versatile fluorescent probe. Royal Society of Chemistry 2015-06-14 2015-05-18 /pmc/articles/PMC4540011/ /pubmed/25985397 http://dx.doi.org/10.1039/c5cc02908b Text en This journal is © The Royal Society of Chemistry 2015 https://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/ (https://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 Mabire, Anne B. Robin, Mathew P. Quan, Wen-Dong Willcock, Helen Stavros, Vasilios G. O'Reilly, Rachel K. Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission |
title | Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
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title_full | Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
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title_fullStr | Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
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title_full_unstemmed | Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
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title_short | Aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission
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title_sort | aminomaleimide fluorophores: a simple functional group with bright, solvent dependent emission |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540011/ https://www.ncbi.nlm.nih.gov/pubmed/25985397 http://dx.doi.org/10.1039/c5cc02908b |
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