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Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions

[Image: see text] Reactions in confined compartments like charged microdroplets are of increasing interest, notably because of their substantially increased reaction rates. When combined with ambient ionization mass spectrometry (MS), reactions in charged microdroplets can be used to improve the det...

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Autores principales: van Geenen, Fred A. M. G., Franssen, Maurice C. R., Zuilhof, Han, Nielen, Michel W. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127799/
https://www.ncbi.nlm.nih.gov/pubmed/30063331
http://dx.doi.org/10.1021/acs.analchem.8b02290
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author van Geenen, Fred A. M. G.
Franssen, Maurice C. R.
Zuilhof, Han
Nielen, Michel W. F.
author_facet van Geenen, Fred A. M. G.
Franssen, Maurice C. R.
Zuilhof, Han
Nielen, Michel W. F.
author_sort van Geenen, Fred A. M. G.
collection PubMed
description [Image: see text] Reactions in confined compartments like charged microdroplets are of increasing interest, notably because of their substantially increased reaction rates. When combined with ambient ionization mass spectrometry (MS), reactions in charged microdroplets can be used to improve the detection of analytes or to study the molecular details of the reactions in real time. Here, we introduce a reactive laser ablation electrospray ionization (reactive LAESI) time-resolved mass spectrometry (TRMS) method to perform and study reactions in charged microdroplets. We demonstrate this approach with a class of reactions new to reactive ambient ionization MS: so-called click chemistry reactions. Click reactions are high-yielding reactions with a high atom efficiency, and are currently drawing significant attention from fields ranging from bioconjugation to polymer modification. Although click reactions are typically at least moderately fast (time scale of minutes to a few hours), in a reactive LAESI approach a substantial increase of reaction time is required for these reactions to occur. This increase was achieved using microdroplet chemistry and followed by MS using the insertion of a reaction tube—up to 1 m in length—between the LAESI source and the MS inlet, leading to near complete conversions due to significantly extended microdroplet lifetime. This novel approach allowed for the collection of kinetic data for a model (strain-promoted) click reaction between a substituted tetrazine and a strained alkyne and showed in addition excellent instrument stability, improved sensitivity, and applicability to other click reactions. Finally, the methodology was also demonstrated in a mass spectrometry imaging setting to show its feasibility in future imaging experiments.
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spelling pubmed-61277992018-09-10 Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions van Geenen, Fred A. M. G. Franssen, Maurice C. R. Zuilhof, Han Nielen, Michel W. F. Anal Chem [Image: see text] Reactions in confined compartments like charged microdroplets are of increasing interest, notably because of their substantially increased reaction rates. When combined with ambient ionization mass spectrometry (MS), reactions in charged microdroplets can be used to improve the detection of analytes or to study the molecular details of the reactions in real time. Here, we introduce a reactive laser ablation electrospray ionization (reactive LAESI) time-resolved mass spectrometry (TRMS) method to perform and study reactions in charged microdroplets. We demonstrate this approach with a class of reactions new to reactive ambient ionization MS: so-called click chemistry reactions. Click reactions are high-yielding reactions with a high atom efficiency, and are currently drawing significant attention from fields ranging from bioconjugation to polymer modification. Although click reactions are typically at least moderately fast (time scale of minutes to a few hours), in a reactive LAESI approach a substantial increase of reaction time is required for these reactions to occur. This increase was achieved using microdroplet chemistry and followed by MS using the insertion of a reaction tube—up to 1 m in length—between the LAESI source and the MS inlet, leading to near complete conversions due to significantly extended microdroplet lifetime. This novel approach allowed for the collection of kinetic data for a model (strain-promoted) click reaction between a substituted tetrazine and a strained alkyne and showed in addition excellent instrument stability, improved sensitivity, and applicability to other click reactions. Finally, the methodology was also demonstrated in a mass spectrometry imaging setting to show its feasibility in future imaging experiments. American Chemical Society 2018-07-31 2018-09-04 /pmc/articles/PMC6127799/ /pubmed/30063331 http://dx.doi.org/10.1021/acs.analchem.8b02290 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle van Geenen, Fred A. M. G.
Franssen, Maurice C. R.
Zuilhof, Han
Nielen, Michel W. F.
Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title_full Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title_fullStr Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title_full_unstemmed Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title_short Reactive Laser Ablation Electrospray Ionization Time-Resolved Mass Spectrometry of Click Reactions
title_sort reactive laser ablation electrospray ionization time-resolved mass spectrometry of click reactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127799/
https://www.ncbi.nlm.nih.gov/pubmed/30063331
http://dx.doi.org/10.1021/acs.analchem.8b02290
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