Department of Chemistry, Sree Neelakanta Government Sanskrit College, Pattambi, Palakkad 679306, Kerala, India.
Department of Applied Chemistry, Cochin University of Science and Technology, Cochin 22, Kerala, India.
J Colloid Interface Sci. 2018 Jun 15;520:70-80. doi: 10.1016/j.jcis.2018.02.077. Epub 2018 Mar 6.
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 HSO 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-yl)-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 6 repeated run.
本文首次报道了一种将碳点掺入多孔椰壳炭中合成磺化催化剂的一锅法。通过扫描电子显微镜(SEM)分析揭示了炭的大孔性质,而通过高分辨率透射电子显微镜(HRTEM)分析则证实了碳点(CDs)在多孔椰壳炭上的分散性。荧光发射光谱进一步证实了催化剂中存在 CDs。材料的傅里叶变换红外(FTIR)光谱分析表明,磺化反应不仅发生在 CD 上,也发生在多孔炭上。最活跃的催化剂的 X 射线光电子能谱(XPS)分析证实了催化剂中存在磺酸基和羧酸基。通过改变 HSO 的用量制备的椰壳炭衍生材料成功用作多组分反应的高效替代绿色催化剂,在无溶剂反应条件下,在短时间内即可获得出色的酰胺基萘酚合成活性。在 N-[苯基-(2-羟基-萘-1-基)-甲基]-苯甲酰胺(代表性的酰胺基萘酚)的合成中,以最佳催化剂在 3 分钟内即可获得 98%的最大产率。该催化剂对各种醛和酰胺的反应具有很高的活性,产物产率在 88-98%之间。即使进行 6 次重复实验,最佳催化剂体系仍保持超过 90%的初始活性。