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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...

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Detalles Bibliográficos
Autores principales: Dacon, Nicholas J., Wu, Nathan B., Michel, Brian W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
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.
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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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