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多孔镍钴双金属催化剂上硼氢化氨脱氢及官能化硝基芳烃的选择性加氢反应

Ammonia borane dehydrogenation and selective hydrogenation of functionalized nitroarene over a porous nickel-cobalt bimetallic catalyst.

作者信息

Miao Hui, Ma Kelong, Zhu Huiru, Yin Kun, Zhang Ying, Cui Yumin

机构信息

School of Chemistry and Materials Engineering, Fuyang Normal University, Anhui Provincial Key Laboratory for Degradation and Monitoring of Pollution of the Environment Fuyang 236037 China

出版信息

RSC Adv. 2019 May 9;9(26):14580-14585. doi: 10.1039/c9ra01551e.

Abstract

The hydrolysis of ammonia borane is a promising strategy for hydrogen energy exploration and exploitation. The produced hydrogen could be directly utilized in hydrogenation reactions. In this work, a bimetallic nickel-cobalt material with porous structure was developed through the pyrolysis of ZIF-67 incorporated with Ni ions. Through the introduction of Ni(NO) as an etching agent, the ZIF-67 polyhedrons were transformed into hollow nanospheres, and further evolved into irregular nanosheets. The bimetallic NiCo phase was formed after pyrolysis in a nitrogen atmosphere at high temperature, with the decomposition and release of organic ligands as gaseous molecules under flowing nitrogen. The obtained bimetallic NiCo porous materials show superior catalytic performance towards hydrolytic dehydrogenation of ammonia borane, thereby nitrobenzene with reducible functional groups can be reduced with high selectivity to the corresponding aniline.

摘要

氨硼烷水解是氢能开发利用的一种很有前景的策略。产生的氢气可直接用于氢化反应。在这项工作中,通过对掺入镍离子的ZIF-67进行热解,制备了一种具有多孔结构的双金属镍钴材料。通过引入硝酸镍作为蚀刻剂,ZIF-67多面体转变为中空纳米球,并进一步演变成不规则纳米片。在高温氮气气氛中热解后形成双金属NiCo相,有机配体在流动氮气下分解并以气态分子形式释放。所制备的双金属NiCo多孔材料对氨硼烷水解脱氢表现出优异的催化性能,因此具有可还原官能团的硝基苯可以高选择性地还原为相应的苯胺。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f29/9064148/6b6da18dd8f1/c9ra01551e-s1.jpg

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