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Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides

This work describes the data collection of new lipophilic esters and amides herbicides, analogues to 2,4-dichlorophenoxyacetic acid (2,4-D) and Propanil. The data include (1)H and (13)C NMR spectra and UV–VIS spectroscopic experiments, from the work “Novel lipophilic analogues from 2,4-D and Propani...

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Detalles Bibliográficos
Autores principales: Porciuncula, Larissa M., Teixeira, Alex R., Santos, Maria F.C., D'Oca, Marcelo G.M., Orth, Elisa S., D'Oca, Caroline R.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482028/
https://www.ncbi.nlm.nih.gov/pubmed/32953952
http://dx.doi.org/10.1016/j.dib.2020.106202
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author Porciuncula, Larissa M.
Teixeira, Alex R.
Santos, Maria F.C.
D'Oca, Marcelo G.M.
Orth, Elisa S.
D'Oca, Caroline R.M.
author_facet Porciuncula, Larissa M.
Teixeira, Alex R.
Santos, Maria F.C.
D'Oca, Marcelo G.M.
Orth, Elisa S.
D'Oca, Caroline R.M.
author_sort Porciuncula, Larissa M.
collection PubMed
description This work describes the data collection of new lipophilic esters and amides herbicides, analogues to 2,4-dichlorophenoxyacetic acid (2,4-D) and Propanil. The data include (1)H and (13)C NMR spectra and UV–VIS spectroscopic experiments, from the work “Novel lipophilic analogues from 2,4-D and Propanil herbicides: Biological activity and kinetic studies”. The UV–VIS and (1)H NMR spectra were employed to kinetic degradation design, and could be used to access new herbicides derivatives with better environmental properties.
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spelling pubmed-74820282020-09-17 Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides Porciuncula, Larissa M. Teixeira, Alex R. Santos, Maria F.C. D'Oca, Marcelo G.M. Orth, Elisa S. D'Oca, Caroline R.M. Data Brief Data Article This work describes the data collection of new lipophilic esters and amides herbicides, analogues to 2,4-dichlorophenoxyacetic acid (2,4-D) and Propanil. The data include (1)H and (13)C NMR spectra and UV–VIS spectroscopic experiments, from the work “Novel lipophilic analogues from 2,4-D and Propanil herbicides: Biological activity and kinetic studies”. The UV–VIS and (1)H NMR spectra were employed to kinetic degradation design, and could be used to access new herbicides derivatives with better environmental properties. Elsevier 2020-08-21 /pmc/articles/PMC7482028/ /pubmed/32953952 http://dx.doi.org/10.1016/j.dib.2020.106202 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Porciuncula, Larissa M.
Teixeira, Alex R.
Santos, Maria F.C.
D'Oca, Marcelo G.M.
Orth, Elisa S.
D'Oca, Caroline R.M.
Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title_full Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title_fullStr Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title_full_unstemmed Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title_short Characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and Propanil herbicides
title_sort characterization data and kinetic studies of novel lipophilic analogues from 2,4-dichlorophenoxyacetic acid and propanil herbicides
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482028/
https://www.ncbi.nlm.nih.gov/pubmed/32953952
http://dx.doi.org/10.1016/j.dib.2020.106202
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