Synthesis of 1,2,4-Triazole Derivatives via 1,3-Benzothiazole-2,5-Diamine Supported on Nanocellulose as Novel Recyclable Nano Catalyst

IF 2.4 3区 化学 Q2 CHEMISTRY, ORGANIC
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引用次数: 0

Abstract

The study aimed to design a novel nanocatalyst, 1,3-Benzothiazole-2,5-diamine supported on nanocellulose (BTDA@CNC), which was characterized using various analytical techniques such as FT-IR, XRD, TGA, SEM, TEM, and CHN. The nanocatalyst was utilized for the synthesis of 1,2,4-triazole derivatives through a simple and efficient three-component reaction between aldehyde derivatives, semicarbazide, and ethanol. The protocol offered advantages such as a simple procedure, high yields, short reaction time, and an environmentally benign method. The nanocatalyst could be readily separated by filter and reused without significant loss of its catalytic efficiency. The synthesized compounds showed moderate activity against both Gram-positive and Gram-negative bacteria, and the antifungal properties of the candida albicans synthesized derivatives were also investigated.
通过纳米纤维素作为新型可回收纳米催化剂支持的 1,3-苯并噻唑-2,5-二胺合成 1,2,4-三唑衍生物
该研究旨在设计一种新型纳米催化剂--纳米纤维素(BTDA@CNC)上支撑的 1,3-苯并噻唑-2,5-二胺,并利用傅立叶变换红外光谱、XRD、TGA、SEM、TEM 和 CHN 等多种分析技术对其进行了表征。利用该纳米催化剂,通过醛衍生物、半咔嗪和乙醇之间简单高效的三组分反应,合成了 1,2,4-三唑衍生物。该方法具有程序简单、产率高、反应时间短和对环境无害等优点。纳米催化剂可以很容易地通过过滤分离出来并重复使用,其催化效率不会明显降低。合成的化合物对革兰氏阳性菌和革兰氏阴性菌都有一定的活性,同时还研究了合成的白念珠菌衍生物的抗真菌特性。
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来源期刊
Polycyclic Aromatic Compounds
Polycyclic Aromatic Compounds 化学-有机化学
CiteScore
3.70
自引率
20.80%
发文量
412
审稿时长
3 months
期刊介绍: The purpose of Polycyclic Aromatic Compounds is to provide an international and interdisciplinary forum for all aspects of research related to polycyclic aromatic compounds (PAC). Topics range from fundamental research in chemistry (including synthetic and theoretical chemistry) and physics (including astrophysics), as well as thermodynamics, spectroscopy, analytical methods, and biology to applied studies in environmental science, biochemistry, toxicology, and industry. Polycyclic Aromatic Compounds has an outstanding Editorial Board and offers a rapid and efficient peer review process, as well as a flexible open access policy.
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