Synthesis and antagonistic evaluation of fluorinated imidazolium salt [1-(2,6-diisopropylphenyl)-3-(2-fluoro-benzyl)-1H-imidazol-3-ium bromide] against significant phytopathogens in agriculture

IF 1.7 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Dhrubajit Borah , Pranaba Nanda Bhattacharyya , Bharat Chandra Nath , Rajashree Chetia , Nazim Forid Islam , Bhaskar Sarma
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Abstract

The current investigation evaluated the in vitro bioefficacy of a newly synthesized unsymmetrical imidazolium salt [1-(2,6-diisopropylphenyl)-3-(2-fluoro-benzyl)-1H-imidazol-3-ium bromide] that contains the electron-withdrawing fluorine atom at the ortho position against agriculturally significant phytopathogens. The molecular structure of the imidazolium salt was characterized by various spectroscopic techniques such as 1H, 13C, and 19F NMR, FTIR, and high-resolution mass spectrometry (HRMS). Antimicrobial bioassay of the compound has been tested against two Gram-negative, bacterial phytopathogens namely Ralstonia solanacearum (Rs) (Gen Bank accession no. OQ743450) [causal agent: bacterial wilt of solanaceous crops], and Xanthomonas citri pv. citri (Xcc) (Gen Bank accession no. OR7036310) [causal agent: citrus canker in citrus trees] and two fungal phytopathogens namely Fusarium solani (Gen Bank accession no. OR140825) [causal agent: Fusarium die-back in tea] and Pseudopestalotiopsis chinensis (Gen Bank accession no. OR140826) [causal agent: grey blight in tea]. Different concentrations of imidazolium salt was tested against the target phytopathogens using the in vitro antimicrobial bioassay through disc diffusion method. The imidazolium salt demonstrated a maximum percentage inhibition of 16.70 and 21.78 against the bacterial phytopathogens R. solanacearum, and X. citri pv. citri, respectively, at a concentration of 2000 ppm over negative control. Similarly, the compound demonstrated promising antagonism against the tea fungal pathogens F. solani and P. chinensis (percentage inhibition up to 61.43 and 80.84, respectively at 2000 ppm) over negative control. Five replications were maintained in each of the cases. The present investigation demonstrated the potential of fluorinated imidazolium salt as commercial antimicrobial agent in integrated disease management schedule to control significant phytopathogenesis in agriculture including in tea.

Abstract Image

氟化咪唑鎓盐[1-(2,6-二异丙基苯基)-3-(2-氟-苄基)-1H-咪唑-3-鎓溴化物]的合成及对农业中重要植物病原体的拮抗评价
目前的研究评估了一种新合成的不对称咪唑鎓盐[1-(2,6-二异丙基苯基)-3-(2-氟-苄基)-1H-咪唑-3-鎓溴化物]的体外生物药效,这种咪唑鎓盐在正交位置含有可吸收电子的氟原子,可防治对农业有重要意义的植物病原体。通过 1H、13C 和 19F NMR、傅立叶变换红外光谱以及高分辨质谱(HRMS)等多种光谱技术对咪唑盐的分子结构进行了表征。该化合物的抗菌生物测定针对两种革兰氏阴性细菌性植物病原体进行了测试,即 Ralstonia solanacearum (Rs)(基因库登录号:OQ743450)[病原:茄科作物细菌性枯萎病]和 Xanthomonas citri pv. citri (Xcc)(基因库登录号:OR7036310)[病原:茄科作物细菌性枯萎病]。OR7036310)[病原:柑橘树柑橘腐烂病]和两种真菌植物病原体,即 Fusarium solani(基因库登录号:OR140825)[病原:茶叶镰刀菌枯萎病]和 Pseudopestalotiopsis chinensis(基因库登录号:OR140826)[病原:茶叶灰霉病]。使用体外抗菌生物测定法,通过圆盘扩散法,对不同浓度的咪唑鎓盐进行了针对目标植物病原体的测试。与阴性对照相比,浓度为 2000 ppm 的咪唑鎓盐对细菌性植物病原体 R. solanacearum 和 X. citri pv. citri 的抑制率最高,分别为 16.70% 和 21.78%。同样,与阴性对照相比,该化合物对茶叶真菌病原体 F. solani 和 P. chinensis 也有很好的拮抗作用(在 2000 ppm 浓度下,抑制率分别达到 61.43 和 80.84)。每种情况都有五个重复。本研究证明了氟化咪唑盐作为商业抗菌剂在综合病害管理计划中控制农业(包括茶叶)中重要植物病原的潜力。
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来源期刊
Journal of Fluorine Chemistry
Journal of Fluorine Chemistry 化学-无机化学与核化学
CiteScore
3.80
自引率
10.50%
发文量
99
审稿时长
33 days
期刊介绍: The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature. For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.
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