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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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Detalles Bibliográficos
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
Descripción
Sumario: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.