2019
DOI: 10.1002/aoc.4832
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Pd‐Pt/modified GO as an efficient and selective heterogeneous catalyst for the reduction of nitroaromatic compounds to amino aromatic compounds by the hydrogen source

Abstract: In this work, different nitroaromatic compounds were successfully reduced to their corresponding aromatic amines with excellent conversion and selectivity in methanol at 50 °C by using Pd‐Pt nanoparticles immobilized on the modified grapheme oxide (m‐GO) and hydrogen as the reducing source. The catalytic efficiency of Pd and Pd‐Pt loading on the modified GO was investigated for the reduction of various nitroaromatic compounds, and the Pd‐Pt/m‐GO system demonstrated the highest conversion and selectivity. The c… Show more

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Cited by 7 publications
(6 citation statements)
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“…They are usually obtained by chemoselective hydrogenation of nitro compound suing H 2 as hydrogen donors, but the selectivity to aromatic amines is low. Hydrogen‐rich ammonia borane (AB) is a promising hydrogen source for selective hydrogenation reactions, but its stable structure makes the release of hydrogen at mild conditions a challenge . In this work, we show that the in situ synthesized Pt–Ni NF@Ni‐MOF‐74 is active for hydrogen release from AB and exhibits excellent selectivity for selective hydrogenation of 4‐nitrostyrenearomatic amines, even being conducted at room temperature (RT), potentiating its great applications for selective hydrogenation reactions.…”
Section: Methodsmentioning
confidence: 59%
“…They are usually obtained by chemoselective hydrogenation of nitro compound suing H 2 as hydrogen donors, but the selectivity to aromatic amines is low. Hydrogen‐rich ammonia borane (AB) is a promising hydrogen source for selective hydrogenation reactions, but its stable structure makes the release of hydrogen at mild conditions a challenge . In this work, we show that the in situ synthesized Pt–Ni NF@Ni‐MOF‐74 is active for hydrogen release from AB and exhibits excellent selectivity for selective hydrogenation of 4‐nitrostyrenearomatic amines, even being conducted at room temperature (RT), potentiating its great applications for selective hydrogenation reactions.…”
Section: Methodsmentioning
confidence: 59%
“…Although the structures listed in Table have not yet been synthesized, to the best of our knowledge, all structures listed in Table can be synthesized from commercially available chemical structures, such as 4-aminobenzene-1,2-diol. These commercially available structures have been studied and can be synthesized from existing methods. …”
Section: Resultsmentioning
confidence: 99%
“…使用氢气催化还原对于生 产苯胺类产物具有环境友好和高效等特点 [19] . 对于含 有取代基的硝基苯化合物还原得到相应的苯胺化合 物是一难题 [20,21] . 已有报道将金属Pd用于该还原反 应 [22] , 但该金属往往选择性较低, 对于含有多个官能…”
Section: 苯胺 特别是含有官能团的苯胺及其衍生物在农unclassified