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Synthesis, characterization, and antifungal activity of novel quaternary chitosan derivatives

机译:新型季铵壳聚糖衍生物的合成,表征和抗真菌活性

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摘要

Three novel quaternary chitosan derivatives were successfully synthesized by reaction of chloracetyl chitosan (CACS) with pyridine (PACS), 4-(5-chloro-2-hydroxybenzylideneamino)-pyridine (CHPACS), and 4-(5-bromo-2-hydroxybenzylideneamino)-pyridine (BHPACS). The chemical structure of the prepared chitosan derivatives was confirmed by Fourier transform infrared (FT-IR) and ~(13)C nuclear magnetic resonance (~(13)C NMR) and their antifungal activity against Cladosporium cucumerinum, Monilinia fructicola, Colletotrichum lagenarium, and Fusarium oxysporum was assessed. Comparing with the antifungal activity of chitosan, CACS, and PACS, CHPACS and BHPACS exhibited obviously better inhibitory effects, which should be related to the synergistic reaction of chitosan itself with the grafted 2-[4-(5-chloro-2-hydroxybenzylideneamino)-pyridyl]acetyl and 2-[4-(5-bromo-2-hydroxybenzylideneamino)-pyridyl]acetyl.
机译:通过氯乙酰壳聚糖(CACS)与吡啶(PACS),4-(5-氯-2-羟基苄叉基氨基)-吡啶(CHPACS)和4-(5-溴-2-羟基苄叉基氨基)反应成功合成了三种新颖的季壳聚糖衍生物)-吡啶(BHPACS)。制备的壳聚糖衍生物的化学结构通过傅里叶变换红外(FT-IR)和〜(13)C核磁共振(〜(13)C NMR)以及它们对黄瓜枝孢菌,莫尼利尼亚果蝇,炭疽菌的抗真菌活性进行了确认,并评价了尖孢镰刀菌。与壳聚糖,CACS和PACS的抗真菌活性相比,CHPACS和BHPACS表现出明显更好的抑制作用,这应与壳聚糖本身与接枝的2- [4-(5-氯-2-羟基苄亚胺基)的协同反应有关。 -吡啶基]乙酰基和2- [4-(5-溴-2-羟基苄叉亚氨基)-吡啶基]乙酰基。

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