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一种六边形共价卟啉框架作为金纳米颗粒催化还原4-硝基苯酚的高效载体。

A Hexagonal Covalent Porphyrin Framework as an Efficient Support for Gold Nanoparticles toward Catalytic Reduction of 4-Nitrophenol.

作者信息

Ding Zheng-Dong, Wang Yu-Xia, Xi Sai-Fei, Li Yunxing, Li Zaijun, Ren Xuehong, Gu Zhi-Guo

机构信息

The Key Laboratory of Food Colloids and Biotechnology, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122, P. R. China.

The Key Laboratory of Eco-textiles of Ministry of Education, College of Textiles and Clothing, Jiangnan University, Wuxi, 214122, P. R. China.

出版信息

Chemistry. 2016 Nov 14;22(47):17029-17036. doi: 10.1002/chem.201603212. Epub 2016 Oct 13.

Abstract

A hexagonal porphyrin-based porous organic polymer, namely, CPF-1, was constructed by 3+2 ketoenamine condensation of the C -symmetric porphyrin diamine 5,15-bis(4-aminophenyl)-10,20-diphenylporphyrin and 1,3,5-triformylphloroglucinol. This material exhibits permanent porosity and excellent thermal and chemical stability. CPF-1 can be employed as a superior supporting substrate to immobilize Au nanoparticles (NPs) as a result of the strong interactions between Au NPs and the CPF support. An Au@CPF-1 hybrid was synthesized by an interfacial solution infiltration method with NaBH as reducing agent. Au NPs (5 nm) grew on CPF-1 and were distributed without aggregation. Moreover, Au@CPF-1 exhibits superior catalytic activity compared to many other reported Au-based catalysts for the reduction of 4-nitrophenol in the presence of NaBH . In addition, Au@CPF-1 has excellent stability and recyclability, and it can be reused for three successive reaction cycles without loss of activity. The dense distribution of phenyl rings on the channel walls of the CPF support can reasonably be regarded as the active sites that adsorb the 4-nitrophenol molecule through hydrogen-bonding and C-H⋅⋅⋅π interactions, as was confirmed by the X-ray structure of model compound DAPP-Benz.

摘要

一种基于六方卟啉的多孔有机聚合物,即CPF-1,通过C对称卟啉二胺5,15-双(4-氨基苯基)-10,20-二苯基卟啉与1,3,5-三甲酰基间苯三酚的3+2酮胺缩合反应构建而成。该材料具有永久孔隙率以及出色的热稳定性和化学稳定性。由于金纳米颗粒(NPs)与CPF载体之间存在强相互作用,CPF-1可作为一种优良的支撑基质来固定金纳米颗粒。以硼氢化钠为还原剂,通过界面溶液渗透法合成了Au@CPF-1杂化物。5纳米的金纳米颗粒生长在CPF-1上且分布均匀无聚集。此外,在硼氢化钠存在下,与许多其他已报道的用于还原4-硝基苯酚的金基催化剂相比,Au@CPF-1表现出优异的催化活性。此外,Au@CPF-1具有出色的稳定性和可回收性,并且可以连续重复使用三个反应循环而不损失活性。CPF载体通道壁上苯环的密集分布可合理地视为通过氢键和C-H⋅⋅⋅π相互作用吸附4-硝基苯酚分子的活性位点,这已通过模型化合物DAPP-苯的X射线结构得到证实。

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