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Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity

A series of novel trifluoromethylcoumarinyl urea derivatives were designed, synthesized, and characterized by (1)H-NMR, (13)C-NMR, and HR-ESI-MS. The fluorescence spectra of the target compounds were recorded. The spectra show that most of the title compounds glow green with λ(max)(em) of 500–517 nm...

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Autores principales: Qiao, Lili, Hao, Shuanghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017327/
https://www.ncbi.nlm.nih.gov/pubmed/29518951
http://dx.doi.org/10.3390/molecules23030600
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author Qiao, Lili
Hao, Shuanghong
author_facet Qiao, Lili
Hao, Shuanghong
author_sort Qiao, Lili
collection PubMed
description A series of novel trifluoromethylcoumarinyl urea derivatives were designed, synthesized, and characterized by (1)H-NMR, (13)C-NMR, and HR-ESI-MS. The fluorescence spectra of the target compounds were recorded. The spectra show that most of the title compounds glow green with λ(max)(em) of 500–517 nm, while compounds 5r, 5s, 5u, and 5l (compounds named by authors) glow violet with λ(max)(em) of 381–443 nm. Moreover, the herbicidal and antifungal activities of the synthesized compounds were evaluated for their potential use as pesticides. The results indicate that compound 5f against the caulis of Amaranthus retroflexus and compounds 5j and 5l against the taproot of Digitaria sanguinalis are equivalent to the commercial herbicide Acetochlor. Nine of the title compounds are more antifungal than commercial fungicide Carbendazim against Botrytis cinerea.
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spelling pubmed-60173272018-11-13 Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity Qiao, Lili Hao, Shuanghong Molecules Article A series of novel trifluoromethylcoumarinyl urea derivatives were designed, synthesized, and characterized by (1)H-NMR, (13)C-NMR, and HR-ESI-MS. The fluorescence spectra of the target compounds were recorded. The spectra show that most of the title compounds glow green with λ(max)(em) of 500–517 nm, while compounds 5r, 5s, 5u, and 5l (compounds named by authors) glow violet with λ(max)(em) of 381–443 nm. Moreover, the herbicidal and antifungal activities of the synthesized compounds were evaluated for their potential use as pesticides. The results indicate that compound 5f against the caulis of Amaranthus retroflexus and compounds 5j and 5l against the taproot of Digitaria sanguinalis are equivalent to the commercial herbicide Acetochlor. Nine of the title compounds are more antifungal than commercial fungicide Carbendazim against Botrytis cinerea. MDPI 2018-03-07 /pmc/articles/PMC6017327/ /pubmed/29518951 http://dx.doi.org/10.3390/molecules23030600 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Qiao, Lili
Hao, Shuanghong
Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title_full Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title_fullStr Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title_full_unstemmed Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title_short Novel Trifluoromethylcoumarinyl Urea Derivatives: Synthesis, Characterization, Fluorescence, and Bioactivity
title_sort novel trifluoromethylcoumarinyl urea derivatives: synthesis, characterization, fluorescence, and bioactivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017327/
https://www.ncbi.nlm.nih.gov/pubmed/29518951
http://dx.doi.org/10.3390/molecules23030600
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