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Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene
A number of Activity-Based Sensors (ABS) for relatively unreactive small molecules, such as ethylene, necessitates a transition metal for reaction under ambient conditions. Olefin metathesis has emerged as one of the primary strategies to achieve ethylene detection, and other transition metals are u...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619136/ https://www.ncbi.nlm.nih.gov/pubmed/37920389 http://dx.doi.org/10.1039/d3cb00079f |
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author | Dacon, Nicholas J. Wu, Nathan B. Michel, Brian W. |
author_facet | Dacon, Nicholas J. Wu, Nathan B. Michel, Brian W. |
author_sort | Dacon, Nicholas J. |
collection | PubMed |
description | A number of Activity-Based Sensors (ABS) for relatively unreactive small molecules, such as ethylene, necessitates a transition metal for reaction under ambient conditions. Olefin metathesis has emerged as one of the primary strategies to achieve ethylene detection, and other transition metals are used for similarly challenging-to-detect analytes. However, limited studies exist investigating how fluorophore-metal attachment impacts photophysical properties of such ABS. Two new probes were prepared with the chelating benzlidene Ru–ligand directly conjugated to a BODIPY fluorophore and the photophysical properties of the new conjugated ABS were evaluated. |
format | Online Article Text |
id | pubmed-10619136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-106191362023-11-02 Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene Dacon, Nicholas J. Wu, Nathan B. Michel, Brian W. RSC Chem Biol Chemistry A number of Activity-Based Sensors (ABS) for relatively unreactive small molecules, such as ethylene, necessitates a transition metal for reaction under ambient conditions. Olefin metathesis has emerged as one of the primary strategies to achieve ethylene detection, and other transition metals are used for similarly challenging-to-detect analytes. However, limited studies exist investigating how fluorophore-metal attachment impacts photophysical properties of such ABS. Two new probes were prepared with the chelating benzlidene Ru–ligand directly conjugated to a BODIPY fluorophore and the photophysical properties of the new conjugated ABS were evaluated. RSC 2023-09-25 /pmc/articles/PMC10619136/ /pubmed/37920389 http://dx.doi.org/10.1039/d3cb00079f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Dacon, Nicholas J. Wu, Nathan B. Michel, Brian W. Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title | Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title_full | Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title_fullStr | Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title_full_unstemmed | Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title_short | Red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
title_sort | red-shifted activity-based sensors for ethylene via direct conjugation of fluorophore to metal–carbene |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619136/ https://www.ncbi.nlm.nih.gov/pubmed/37920389 http://dx.doi.org/10.1039/d3cb00079f |
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