化学
转移加氢
苯酚
氨硼烷
电子转移
钯
纳米颗粒
金属有机骨架
还原剂
硝基
金属
核化学
催化作用
氢气储存
无机化学
药物化学
氢
有机化学
化学工程
钌
吸附
烷基
工程类
作者
Valle Krishnaveni,Marilyn Esclance DMello,K. Basavaiah,Dasi Samsonu,Dheer A. Rambhia,Suresh Babu Kalidindi
标识
DOI:10.1002/ejic.202200314
摘要
Abstract Metal‐organic frameworks (MOFs) are crystalline porous materials with designable pores. In this study, we loaded Pd nanoparticles onto π‐electron rich pores of ellagic acid based SU‐101 MOF (Bi 2 O(H 2 O) 2 (C 14 H 2 O 8 ) ⋅ nH 2 O) in order to surround Pd active sites with π‐electron rich environment. The material has been explored for the transformation of 4‐Nitro phenol (4‐NP) to 4‐Amino phenol (4‐AP) using ammonia borane (AB). AB acted as efficient transfer hydrogenation agent compared to NaBH 4 because of its ability to transfer hydrogens at milder conditions. AB is safer and easy to handle compared to molecular hydrogen or NaBH 4 . The Pd NPs are loaded on to SU‐101 using two methodologies. One by supporting preformed Pd NPs onto MOF surface (Pd‐WCGA/SU‐101) and the other by wet impregnation method (Pd/SU‐101). The later method yields a material with strong interaction between Pd and SU‐101. The Pd/SU‐101 exhibited superior activity for 4‐NP reduction (turn over frequency=2421 h −1 ) using AB due to an enrichment of 4‐NP around Pd active sites by π‐electron rich pore environment.
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