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HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance
The oxidative coupling of imines to ketazine with molecular oxygen is a green process towards the synthesis of hydrazine or hydrazine hydrate, which could efficiently address the economic and environmental issues of the traditional Raschig or peroxide-ketazine process. Herein, we developed an effici...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056984/ https://www.ncbi.nlm.nih.gov/pubmed/35517087 http://dx.doi.org/10.1039/d0ra06367c |
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author | Kaimeng, Huang Siyuan, Chen Changjiu, Xia Chenhao, Li Bin, Zhu Hongyi, Gao Xinxin, Peng Min, Lin Yibin, Luo Ge, Wang Xingtian, Shu |
author_facet | Kaimeng, Huang Siyuan, Chen Changjiu, Xia Chenhao, Li Bin, Zhu Hongyi, Gao Xinxin, Peng Min, Lin Yibin, Luo Ge, Wang Xingtian, Shu |
author_sort | Kaimeng, Huang |
collection | PubMed |
description | The oxidative coupling of imines to ketazine with molecular oxygen is a green process towards the synthesis of hydrazine or hydrazine hydrate, which could efficiently address the economic and environmental issues of the traditional Raschig or peroxide-ketazine process. Herein, we developed an efficient heterogeneous base-free benzophenone imine oxidative coupling route with O(2) catalyzed by Cu/CuO(x)/carbon materials derived from MOFs under mild conditions. Under optimized conditions, the conversion of BI is up to 98.2% and the selectivity of ketamine is 94.9%. This catalyst has excellent structure stability, recycling, and regeneration performance, owing to the carbonization of organic ligands of MOF at high temperature. More importantly, it is confirmed that the metallic Cu core is essential to improve the catalytic performance of the CuO shell in the BI oxidative coupling reaction, due to the promotion of electron transfer in the CuO surface, making dissolved O(2) molecules more easily insert oxygen vacancies. This strategy might open an avenue to the sustainable catalytic synthesis of hydrazine or hydrazine hydrate. |
format | Online Article Text |
id | pubmed-9056984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90569842022-05-04 HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance Kaimeng, Huang Siyuan, Chen Changjiu, Xia Chenhao, Li Bin, Zhu Hongyi, Gao Xinxin, Peng Min, Lin Yibin, Luo Ge, Wang Xingtian, Shu RSC Adv Chemistry The oxidative coupling of imines to ketazine with molecular oxygen is a green process towards the synthesis of hydrazine or hydrazine hydrate, which could efficiently address the economic and environmental issues of the traditional Raschig or peroxide-ketazine process. Herein, we developed an efficient heterogeneous base-free benzophenone imine oxidative coupling route with O(2) catalyzed by Cu/CuO(x)/carbon materials derived from MOFs under mild conditions. Under optimized conditions, the conversion of BI is up to 98.2% and the selectivity of ketamine is 94.9%. This catalyst has excellent structure stability, recycling, and regeneration performance, owing to the carbonization of organic ligands of MOF at high temperature. More importantly, it is confirmed that the metallic Cu core is essential to improve the catalytic performance of the CuO shell in the BI oxidative coupling reaction, due to the promotion of electron transfer in the CuO surface, making dissolved O(2) molecules more easily insert oxygen vacancies. This strategy might open an avenue to the sustainable catalytic synthesis of hydrazine or hydrazine hydrate. The Royal Society of Chemistry 2020-10-01 /pmc/articles/PMC9056984/ /pubmed/35517087 http://dx.doi.org/10.1039/d0ra06367c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Kaimeng, Huang Siyuan, Chen Changjiu, Xia Chenhao, Li Bin, Zhu Hongyi, Gao Xinxin, Peng Min, Lin Yibin, Luo Ge, Wang Xingtian, Shu HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title | HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title_full | HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title_fullStr | HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title_full_unstemmed | HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title_short | HKUST-1 derived Cu@CuO(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
title_sort | hkust-1 derived cu@cuo(x)/carbon catalyst for base-free aerobic oxidative coupling of benzophenone imine: high catalytic efficiency and excellent regeneration performance |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056984/ https://www.ncbi.nlm.nih.gov/pubmed/35517087 http://dx.doi.org/10.1039/d0ra06367c |
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