Copper(I)-chitin biopolymer based: An efficient and recyclable catalyst for click azide–alkyne cycloaddition reactions in water

被引:0
作者
Bahsis, Lahoucine [1 ,2 ]
Ablouh, El-Houssaine [3 ]
Hachim, Mouhi Eddine [4 ]
Anane, Hafid [2 ]
Taourirte, Moha [5 ]
Julve, Miguel [6 ]
Stiriba, Salah-Eddine [6 ]
机构
[1] Laboratoire de Chimie de Coordination et d'Analytique (LCCA), Département de Chimie, Faculté des Sciences d'El Jadida, Université Chouaïb Doukkali, El Jadida, Morocco
[2] Laboratoire de Chimie Analytique et Moléculaire, LCAM, Faculté Polydisciplinaire de Safi, Université Cadi Ayyad, Safi, Morocco
[3] Materials Science and Nanoengineering Department (MSN), Mohammed VI Polytechnic University (UM6P), Ben Guerir, Morocco
[4] Équipe de Modélisation Moléculaire et de Spectroscopie, Faculté des sciences, Université de Chouaïb Doukkali, El Jadida, Morocco
[5] Laboratoire de Chimie Bioorganique et Macromoléculaire, Faculté des Sciences et Techniques de Marrakech, Université Cadi Ayyad, Marrakech, Morocco
[6] Instituto de Ciencia Molecular/ICMol, Universidad de Valencia, Valencia, Spain
来源
Applied Organometallic Chemistry | 2021年 / 35卷 / 08期
关键词
Scanning electron microscopy - Spectroscopic analysis - Cycloaddition - Synthesis (chemical) - Catalysis - Hydrocarbons - Biomolecules - Catalyst activity - Reusability - Biopolymers - Regioselectivity;
D O I
暂无
中图分类号
学科分类号
摘要
The naturally occurring α-chitin biopolymer was employed for the immobilisation of copper(I) ion, resulting into a new bioconjugate complex, namely, Cu(I)-α-chitin (CuI-CHT) with catalytic efficiency in copper-catalysed azide–alkyne cycloaddition reactions (click chemistry, CuAAC). The prepared catalyst was characterised by using spectroscopic and analytical methods such as Fourier-transform infrared (FT-IR), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), X-ray diffraction (XRD) and inductively coupled plasma (ICP) analysis. The catalytic activity of CuI-CHT was investigated in the [3 + 2] cycloaddition reactions of alkynes and organic azides for the regioselective click of 1,4-disubstituted-1,2,3-triazole derivatives in water at room temperature. The catalytic results indicate that the prepared CuI-CHT catalyst led to a high yield with a regioselective synthesis of the corresponding 1,4-disubstituted-1,2,3-triazoles under strict click conditions. The reusability and simple recovery of this catalyst make it a suitable sustainable catalyst for CuAAC reactions. © 2021 John Wiley & Sons, Ltd.
引用
收藏
相关论文
empty
未找到相关数据