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At present, it is highly important to develop nanopesticide, which can improve the effect of pesticides and reduce the risks of environmental. Zeolitic imidazolate framework (ZIF) is usually used as a nanocarrier of nanopesticide, which has a porous structure and stimuli-responsive properties. However, the drug loading performance and stability of ZIF are poor. To solve these disadvantages, we successfully prepared bimetallic ZIF nanocarriers by hybridizing and structurally regulating ZIF-L with Co. Here, we propose that Zn and Co bimetallic ZIF (ZnCo-ZIF) was used for efficient loading and controlled release of thiamethoxam (THX). Notably, the specific surface area of ZnCo-ZIF with flower-cluster structure was 8.7338 m/g, which could provide a large number of active sites for THX loading. Besides, it was found that the maximum THX loading rate of ZnCo-ZIF was 12.7% by optimizing the load experimental conditions, which was 1.4 times higher than that initial. After that, ZnCo-ZIF@THX was modified by the metal-phenol network (MPN), which formed through the chelation of tannic acid (TA) and iron ions. In the PBS release medium, the cumulative release rate of the ZnCo-ZIF@THX@MPN reaches 100% for 24h. In addition, the photostability of ZnCo-ZIF@THX@MPN had been greatly improved, which the photodegradation half-life of it was 4.17 times that of THX technical drug. After MPN encapsulation, the maximum retention and rainwater resistance of the nanopesticide on vegetable leaves were also improved. The bemisia tabaci was used as the model insect, and the mortality of ZnCo-ZIF@THX@MPN against was increased to 88.15%. Finally, the safety experiment shows ZnCo-ZIF@THX@MPN had no inhibitory effect on pakchoi seed germination and had good biosafety. This work provides a new idea for the development that the facile synthesis of bimetallic flower-cluster nanocarriers and load of thiamethoxam.
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http://dx.doi.org/10.1016/j.envres.2025.120753 | DOI Listing |
Org Lett
September 2025
United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan.
A direct azidomethylation reaction at the sulfur atoms of thiols with -azidomethyldisulfonimides is presented, providing a facile and efficient approach for the synthesis of azidomethylated compounds with broad substrate scope and mild reaction conditions. Under optimized conditions using -azidomethyl-bis(4-trifluoromethylbenzene)sulfonimide as the azidomethyl source, various aliphatic and aromatic thiols furnish the corresponding -azidomethyl compounds in moderate to high yields. The reaction proceeds selectively at the mercapto group, even in substrates bearing polar functional groups.
View Article and Find Full Text PDFOrg Lett
September 2025
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, P. R. China.
A visible-light-induced cascade annulation of -cyanamide alkenes with unsaturated α-halogenocarbonyls for the facile synthesis of piperidino-quinazolinone derivatives has been developed. This transformation simultaneously constructs three C-C bonds, one C-N bond, and three cyclic structures through a cascade process involving alkyl radical addition to alkene followed by three radical annulations. The reaction proceeds under mild conditions and demonstrates a high bond-forming efficiency.
View Article and Find Full Text PDFNat Commun
September 2025
Life-Like Materials and Systems, University of Mainz, Mainz, Germany.
Nuclear biomolecular condensates are essential sub-compartments within the cell nucleus and play key roles in transcription and RNA processing. Bottom-up construction of nuclear architectures in synthetic settings is non-trivial but vital for understanding the mechanisms of condensates in real cellular systems. Here, we present a facile and versatile synthetic DNA protonucleus (PN) platform that facilitates localized transcription of branched RNA motifs with kissing loops (KLs) for subsequent condensation into complex condensate architectures.
View Article and Find Full Text PDFLangmuir
September 2025
Laboratory of Electrochemistry-Corrosion, Metallurgy and Inorganic Chemistry, Faculty of Chemistry, USTHB, BP 32, 16111, Algiers, Algeria.
Azo dyes, prevalent in various industries, including textile dyeing, food, and cosmetics, pose significant environmental and health risks due to their chemical stability and toxicity. This study introduces the synthesis and application of a copper hydrogen-π-bonded benzoate framework (Cu-HBF) and its derived marigold flower-like copper oxide (MFL-CuO) in a synergetic adsorption-photocatalytic process for efficiently removing cationic azo dyes from water, specifically crystal violet (CV), methylene blue (MB), and rhodamine B (RhB). The Cu-HBF, previously available only in single crystal form, is prepared here as a crystalline powder for the first time, using a low-cost and facile procedure, allowing its application as an adsorbent and also serving as a precursor for synthesizing well-structured copper oxide (MFL-CuO).
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Institute of Organometallic Chemistry, Russian Academy of Sciences, Tropinina 49, GSP-445, Nizhny Novgorod 603950, Russia.
In this work, an approach enabling the synthesis of η-alkene lithium complexes (Carb)Li(η-L) (L = 1-octene, cyclohexene) is elaborated. For 1,5-hexadiene, the same approach results in a binuclear μ-η:η-diene complex. The QTAIM parameters reveal the electrostatic nature of the Li-alkene interaction.
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