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Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction

Fabricating efficient and stable nanocatalysts for chemoselective hydrogenation of nitroaromatics is highly desirable because the amines hold tremendous promise for the synthesis of nitrogen containing chemicals. Here, a highly reactive and stable porous carbon nitride encapsulated magnetically holl...

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Autores principales: Ai, Yongjian, Hu, Zenan, Liu, Lei, Zhou, Junjie, Long, Yang, Li, Jifan, Ding, Mingyu, Sun, Hong‐Bin, Liang, Qionglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446610/
https://www.ncbi.nlm.nih.gov/pubmed/30989031
http://dx.doi.org/10.1002/advs.201802132
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author Ai, Yongjian
Hu, Zenan
Liu, Lei
Zhou, Junjie
Long, Yang
Li, Jifan
Ding, Mingyu
Sun, Hong‐Bin
Liang, Qionglin
author_facet Ai, Yongjian
Hu, Zenan
Liu, Lei
Zhou, Junjie
Long, Yang
Li, Jifan
Ding, Mingyu
Sun, Hong‐Bin
Liang, Qionglin
author_sort Ai, Yongjian
collection PubMed
description Fabricating efficient and stable nanocatalysts for chemoselective hydrogenation of nitroaromatics is highly desirable because the amines hold tremendous promise for the synthesis of nitrogen containing chemicals. Here, a highly reactive and stable porous carbon nitride encapsulated magnetically hollow platinum nanocage is developed with subnanometer thick walls (Fe(3)O(4)@snPt@PCN) for this transformation. This well‐controlled nanoreactor is prepared via the following procedures: the preparation of core template, the deposition of platinum nanocage with subnanometer thick walls, oxidative etching, and calcination. This highly integrated catalyst demonstrates excellent performance for the catalytic transfer hydrogenation of various nitroaromatics and the reaction can reach >99% conversion and >99% selectivity. With the ultrathin wall structure, the atom utilization of platinum atoms is highly efficient. The X‐ray photoelectron spectroscopy results indicate that partial electrons transfer from the iron oxides to Pt nanowalls, and this increases the electron density of snPt nanoparticles, thus promoting the catalytic activity for the transfer hydrogenation of nitroaromatics. For the reduction of 4‐nitrophenol, the reaction rate constant K (app) is 0.23 min(−1) and the turnover frequency (TOF) is up to 3062 h(−1). Additional reaction results illustrate that this magnetic nanoreactor can be reused more than eight times and it is a promising catalytic nanoplatform in heterogeneous catalysis.
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spelling pubmed-64466102019-04-15 Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction Ai, Yongjian Hu, Zenan Liu, Lei Zhou, Junjie Long, Yang Li, Jifan Ding, Mingyu Sun, Hong‐Bin Liang, Qionglin Adv Sci (Weinh) Full Papers Fabricating efficient and stable nanocatalysts for chemoselective hydrogenation of nitroaromatics is highly desirable because the amines hold tremendous promise for the synthesis of nitrogen containing chemicals. Here, a highly reactive and stable porous carbon nitride encapsulated magnetically hollow platinum nanocage is developed with subnanometer thick walls (Fe(3)O(4)@snPt@PCN) for this transformation. This well‐controlled nanoreactor is prepared via the following procedures: the preparation of core template, the deposition of platinum nanocage with subnanometer thick walls, oxidative etching, and calcination. This highly integrated catalyst demonstrates excellent performance for the catalytic transfer hydrogenation of various nitroaromatics and the reaction can reach >99% conversion and >99% selectivity. With the ultrathin wall structure, the atom utilization of platinum atoms is highly efficient. The X‐ray photoelectron spectroscopy results indicate that partial electrons transfer from the iron oxides to Pt nanowalls, and this increases the electron density of snPt nanoparticles, thus promoting the catalytic activity for the transfer hydrogenation of nitroaromatics. For the reduction of 4‐nitrophenol, the reaction rate constant K (app) is 0.23 min(−1) and the turnover frequency (TOF) is up to 3062 h(−1). Additional reaction results illustrate that this magnetic nanoreactor can be reused more than eight times and it is a promising catalytic nanoplatform in heterogeneous catalysis. John Wiley and Sons Inc. 2019-02-07 /pmc/articles/PMC6446610/ /pubmed/30989031 http://dx.doi.org/10.1002/advs.201802132 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Ai, Yongjian
Hu, Zenan
Liu, Lei
Zhou, Junjie
Long, Yang
Li, Jifan
Ding, Mingyu
Sun, Hong‐Bin
Liang, Qionglin
Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title_full Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title_fullStr Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title_full_unstemmed Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title_short Magnetically Hollow Pt Nanocages with Ultrathin Walls as a Highly Integrated Nanoreactor for Catalytic Transfer Hydrogenation Reaction
title_sort magnetically hollow pt nanocages with ultrathin walls as a highly integrated nanoreactor for catalytic transfer hydrogenation reaction
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446610/
https://www.ncbi.nlm.nih.gov/pubmed/30989031
http://dx.doi.org/10.1002/advs.201802132
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