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Updated: Feb 26, 2026

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
Schiff Base- and Imidazole-Functionalized Cellulose-Supported Pd Catalyst for 4-Nitrophenol Reduction and Suzuki
JiaJun Bi1, TianHao Chen1, ZeWei Li1
1School of Chemical and Environmental Engineering, Anhui Polytechnic University, Wuhu 241000, PR China.
Abstract:
Cellulose is highly valuable due to its ready availability, biodegradability, and easy chemical modification. Recently, studies have focused on the chemical modification of cellulose and utilized it as a support for stabilizing metals. In this study, a Schiff base- and imidazole-functionalized cellulose-supported Pd (Cell-SB-IM-Pd) catalyst was prepared and used for the 4-nitrohpenol reduction as well as the synthesis of biaryls. Compared with the raw Cell-Pd catalyst (70%), Cell-SB-IM-Pd exhibited higher catalytic efficiency (90%) in Suzuki reactions, which was attributed to the introduction of C═N and imidazole, providing charge-transfer interaction between them and Pd. The Cell-SB-IM-Pd also showed good to excellent yields (up to 99%) for various substrates in Suzuki reactions under mild conditions. Likewise, we also demonstrated the stability and efficiency of Cell-SB-IM-Pd in the 4-nitrophenol reduction at room temperature in water, with an apparent rate constant of 9.074 × 10-2 min-1. This work provides more insights into the further utilization of cellulose as a Pd host matrix for converting organic pollutants and promoting sustainable chemical reactions.
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