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首页> 外文期刊>Journal of Colloid and Interface Science >Functionalized carbon dot adorned coconut shell char derived green catalysts for the rapid synthesis of amidoalkyl naphthols
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Functionalized carbon dot adorned coconut shell char derived green catalysts for the rapid synthesis of amidoalkyl naphthols

机译:官能化的碳点装饰椰子壳Char衍生的绿色催化剂,用于快速合成氨基烷基萘酚

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摘要

A one pot synthesis of carbon dot incorporated porous coconut shell char derived sulphonated catalyst is reported here for the first time and is effectively used in the multicomponent synthesis of amidoalkyl naphthol. Macroporous nature of the char is revealed from scanning electron microscopic (SEM) analysis, whereas the dispersion of carbon dots (CDs) on the porous coconut shell char is confirmed from the high resolution transmission electron microscopic (HRTEM) analysis. Fluorescence emission spectrum further confirmed the presence of CDs in the catalyst. Fourier-transform infrared (FTIR) spectral analysis of the materials indicated that sulphonation occurred both to the CD and to the porous char. X-ray photo electron spectroscopic (XPS) analysis of the most active catalyst confirmed the presence of both sulphonic acid and carboxylic acid groups in the catalyst. The coconut shell char derived materials prepared by varying the amount of H2SO4 are successfully utilized as efficient alternative green catalysts for the multicomponent reaction, where excellent activity in amidoalkyl naphthol synthesis is obtained within short periods under solvent free reaction conditions. A maximum yield of 98% is obtained in the synthesis of N-[Phenyl-(2-hydroxy-naphthalen-1-y1)-methyl]-benzamide, the representative amidoalkyl naphthol, with the best catalyst within 3 min of reaction. The catalyst is highly active for the reactions carried out with varieties of aldehydes and amides with a product yield in the range of 88-98%. The best catalyst system retained more than 90% of its initial activity even upto 6th repeated run. (C) 2018 Elsevier Inc. All rights reserved.
机译:碳点掺入的一个罐合成多孔椰子壳ChOr衍生的磺酸催化剂在此首次介绍,并有效地用于萘烷基萘酚的多组分合成中。从扫描电子显微镜(SEM)分析中揭示了CHAR的大孔性质,而碳点(CDS)在多孔椰子壳壳上的分散从高分辨率透射电子显微镜(HRTEM)分析中确认。荧光发射光谱进一步证实了催化剂中Cd的存在。傅里叶变换红外(FTIR)材料的光谱分析表明,磺化既不发生CD和多孔炭。最活性催化剂的X射线照片电子光谱(XPS)分析证实了催化剂中磺酸和羧酸基团的存在。通过改变H 2 SO 4的量制备的椰子壳CHAR衍生材料作为多组分反应成功地利用了用于多组分反应的有效替代的绿色催化剂,其中在溶剂无反应条件下的短时间内获得氨基烷基萘酚合成的优异活性。在N-[苯基 - (2-羟基 - 萘-1- y1) - 甲酰胺,代表性氨基烷基萘酚的合成中获得最大产率为98%,在3分钟内用最佳催化剂。催化剂非常活跃,对于用品种的醛和产物产率为88-98%的酰胺进行的反应。最佳催化剂系统甚至仍然高达90%的初始活动,甚至可以重复延续。 (c)2018 Elsevier Inc.保留所有权利。

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