A reusable polymer-supported copper(I) catalyst for triazole click reaction on water: An experimental and computational study

被引:48
作者
Bahsis, Lahoucine [1 ]
Ben El Ayouchia, Hicham [1 ]
Anane, Hafid [1 ]
Pascual-Alvarez, Alejandro [2 ]
De Munno, Giovanni [3 ]
Julve, Miguel [2 ]
Stiriba, Salah-Eddine [1 ,2 ]
机构
[1] Univ Cadi Ayyad, Fac Polydisciplinaire Safi, LCAM, Safi, Morocco
[2] Univ Valencia, Inst Ciencia Mol ICMol, C Catedrat Jose Beltran 2, Valencia 46980, Spain
[3] Univ Calabria, Dipartimento Chim & Tecnol Chim, I-87036 Cosenza, Italy
关键词
aminomethyl polystyrene; click chemistry; CuAAC reaction; DFT methods; heterogeneous catalysis; AZIDE-ALKYNE CYCLOADDITION; 1,3-DIPOLAR CYCLOADDITIONS; HETEROGENEOUS CATALYSTS; HUISGEN CYCLOADDITION; REACTION-MECHANISM; POLYSTYRENE RESIN; TERMINAL ALKYNES; HIGHLY EFFICIENT; SOLID-PHASE; CHEMISTRY;
D O I
10.1002/aoc.4669
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the search for establishing a clickable copper-catalysed (3 + 2) Huisgen azide-alkyne cycloaddition (CuAAC) reaction under strict conditions, in particular in terms of preventing the presence of copper particles/traces in reaction products and using an environmentally benign medium such as water, we describe here the synthesis of an aminomethyl polystyrene-supported copper(I) catalyst (Cu(I)-AMPS) and its characterization by means of Fourier transform infrared and energy-dispersive X-ray spectroscopies and scanning electron microscopy. Cu(I)-AMPS was found to be highly active in the CuAAC reaction of various organic azides with alkynes affording the corresponding 1,4-disubstituted 1,2,3-triazoles in a regioselective manner in air at room temperature and using water as solvent. The insolubility and/or partial solubility of the organic azide and alkyne precursors as well as the heterogeneous Cu(I)-AMPS catalytic system points to the occurrence of the cycloaddition at the organic-water interface 'on water' affording quantitative yields of waterinsoluble 1,2,3-triazoles. A mechanistic study was performed using density functional theory aiming at explaining the observed reactivity and selectivity of the Cu (I)-AMPS catalyst in CuAAC reactions.
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页数:15
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