Boosting catalytic activity of π-π interactions-stabilized PdNPs for water-mediated Suzuki couplings of aryl chlorides

Abstract

Utilizing unique interactions to enhance the catalytic performance of supported metal catalysts is a crucial strategy in catalyst design, albeit one that presents a significant challenge. This study introduces an original approach involving the use of π-π interactions to stabilize palladium nanoparticles (PdNPs) with a 2Br-substituted imidazolium-based covalent organic framework (COF, IHP-Br-PdNPs) for efficient water-mediated Suzuki reactions involving deactivated aryl chlorides and arylboronic acids at ambient conditions. Through extensive structural characterization employing techniques including Fourier transform infrared spectroscopy (FT-IR), cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS ¹³C NMR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), N₂ adsorption, and X-ray photoelectron spectroscopy (XPS), we demonstrate the immobilization of highly stable and well-dispersed PdNPs was obtained. The designed IHP-Br-PdNPs demonstrate stability for up to 36 months in ambient air and can be efficiently recycled. After 9 catalytic cycles, there was no significant decline in catalytic performance, and the particle size of PdNPs remained constant at approximately 4–8 nm throughout the reactions. The coordination mode between the stabilizer and metal, specifically the π-π interaction between the 2Br-substituted imidazolium moiety and the Pd metal surface, plays a key role in stabilizing various active species and facilitating distinct catalytic pathways. This study provides valuable insights into the development of π-π interactions supported metal catalysts, which enhance stability and catalytic activity in advanced water-mediated synthesis applications.