摘要
Support materials play a significant role in heterogeneous nanocatalysis.In this work,β-cyclodextrin(β-CD)was used directly as a monomer to construct polymer networks for gold nanoparticles(Au NPs)immobilization.Using the simple nucleophilic substitution reaction,β-CD based polymer networks(β-CDP-N andβ-CDP-C)were successfully prepared.Compared toβ-CDP-C,the hydroxyl groups and N atoms inβ-CDP-N played a synergistic role in immobilizing smaller Au NPs,thus leading to high catalytic activities.Notably,the apparent rate constant(Kapp)value for Au@β-CDP-N in the reduction of 4-nitrophenol to 4-aminophenol is 14.15×10^(-2)s^(-1),which shows a significant improvement over all previously reported Au NPs with solid supports under similar conditions.Considering the negligible porosity of theβ-CDP-N support,we purposed a"capture-catalysis-release"model to explain the high catalytic activity of Au@β-CDP-N.This explanation is supported by the guest-responsive properties ofβ-CDP-N.Moreover,the Au@β-CDP-N is easily recycled and maintained its high catalytic efficiency after seven successful cycles.
基金
the National Natural Science Foundation of China(Nos.21865003,21562003)
China Postdoctoral Science Foundation(No.2018M640114)
National Undergraduate Training Programs for Innovation and Entrepreneurship(No.201910418003)
the Gannan Normal University Innovation Fund(No.YCX19A002)for generous support.