Highly modulated supported triazolium-based ionic liquids: direct control of the electronic environment on Cu nanoparticles. Issue 3 (2nd March 2020)

• Record Type: Journal Article
• Authors: Valdebenito, Cristián; Pinto, Jose; Nazarkovsky, Michael; Chacón, Gustavo; Martínez-Ferraté, Oriol; Wrighton-Araneda, Kerry; Cortés-Arriagada, Diego; Camarada, María Belén; Alves Fernandes, Jesum; Abarca, Gabriel
• Is Part Of: Nanoscale advances. Volume 2:Issue 3(2020)
• Page Start: 1325
• Page End: 1332
• Publication Date: 2020-03-02
• Subjects: 620.5
• DOI: 10.1039/d0na00055h
• Languages: English
• ISSNs: 2516-0230

Abstract

Abstract : A series of new triazolium-based supported ionic liquids (SILPs), decorated with Cu NPs, were successfully prepared and applied to the N -arylation of aryl halides with anilines. Abstract : A series of new triazolium-based supported ionic liquids (SILPs), decorated with Cu NPs, were successfully prepared and applied to the N-arylation of aryl halides with anilines. The triazoles moieties were functionalised using copper-catalysed azide–alkyne cycloaddition. SILP surface characterisation showed a strong correlation between the triazolium cation volume and textural properties. STEM images showed well-dispersed Cu NPs on SILPs with a mean diameter varying from 3.6 to 4.6 nm depending on the triazolium cation used. Besides, XPS results suggest that the Cu(0)/Cu(i ) ratio can be modulated by the electronic density of triazolium substituents. XPS and computational analysis gave mechanistic insights into the Cu NP stabilisation pathways, where the presence of electron-rich groups attached to a triazolium ring plays a critical role in leading to a cation adsorption pathway ( E ads = 72 kcal mol −1 ). In contrast, less electron-rich groups favour the anion adsorption pathway ( E ads = 63 kcal mol −1 ). The Cu@SILP composite with electron-rich groups showed the highest activity for the C–N Ullmann coupling reaction, which suggests that electron-rich groups might act as an electron-like reservoir to facilitate oxidative addition for N-arylation. This strategy firmly suggests the strong dependence of the nature of triazolium-based SILPs on the Cu NP surface active sites, which may provide a new environment to confine and stabilise MNPs for catalytic applications.