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(13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups

[Image: see text] (13)C NMR spectroscopic integration employing short relaxation delays was evaluated as a quantitative tool to obtain ratios of diastereomers, regioisomers, constitutional isomers, mixtures of unrelated compounds, peptoids, and sugars. The results were compared to established quanti...

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Autores principales: Otte, Douglas A. L., Borchmann, Dorothee E., Lin, Chin, Weck, Marcus, Woerpel, K. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993867/
https://www.ncbi.nlm.nih.gov/pubmed/24601654
http://dx.doi.org/10.1021/ol403776k
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author Otte, Douglas A. L.
Borchmann, Dorothee E.
Lin, Chin
Weck, Marcus
Woerpel, K. A.
author_facet Otte, Douglas A. L.
Borchmann, Dorothee E.
Lin, Chin
Weck, Marcus
Woerpel, K. A.
author_sort Otte, Douglas A. L.
collection PubMed
description [Image: see text] (13)C NMR spectroscopic integration employing short relaxation delays was evaluated as a quantitative tool to obtain ratios of diastereomers, regioisomers, constitutional isomers, mixtures of unrelated compounds, peptoids, and sugars. The results were compared to established quantitative methods such as (1)H NMR spectroscopic integration, gas chromatography, and high-performance liquid chromatography and were found to be within <3.4% of (1)H NMR spectroscopic values (most examples give results within <2%). Acquisition of the spectra took 2–30 min on as little as 10 mg of sample, proving the general utility of the technique. The simple protocol was extended to include end group analysis of low molecular weight polymers, which afforded results in accordance with (1)H NMR spectroscopy and matrix-assisted laser desorption-ionization time-of-flight spectrometry.
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spelling pubmed-39938672015-03-06 (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups Otte, Douglas A. L. Borchmann, Dorothee E. Lin, Chin Weck, Marcus Woerpel, K. A. Org Lett [Image: see text] (13)C NMR spectroscopic integration employing short relaxation delays was evaluated as a quantitative tool to obtain ratios of diastereomers, regioisomers, constitutional isomers, mixtures of unrelated compounds, peptoids, and sugars. The results were compared to established quantitative methods such as (1)H NMR spectroscopic integration, gas chromatography, and high-performance liquid chromatography and were found to be within <3.4% of (1)H NMR spectroscopic values (most examples give results within <2%). Acquisition of the spectra took 2–30 min on as little as 10 mg of sample, proving the general utility of the technique. The simple protocol was extended to include end group analysis of low molecular weight polymers, which afforded results in accordance with (1)H NMR spectroscopy and matrix-assisted laser desorption-ionization time-of-flight spectrometry. American Chemical Society 2014-03-06 2014-03-21 /pmc/articles/PMC3993867/ /pubmed/24601654 http://dx.doi.org/10.1021/ol403776k Text en Copyright © 2014 American Chemical Society
spellingShingle Otte, Douglas A. L.
Borchmann, Dorothee E.
Lin, Chin
Weck, Marcus
Woerpel, K. A.
(13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title_full (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title_fullStr (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title_full_unstemmed (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title_short (13)C NMR Spectroscopy for the Quantitative Determination of Compound Ratios and Polymer End Groups
title_sort (13)c nmr spectroscopy for the quantitative determination of compound ratios and polymer end groups
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993867/
https://www.ncbi.nlm.nih.gov/pubmed/24601654
http://dx.doi.org/10.1021/ol403776k
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