Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates
In this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO3. In the reaction, the conversion rate and product selectivity could be both as high as 95% in N2 atmosphere, while the benzaldehyde yield also reached 85% in...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-03-01
|
Series: | Frontiers in Chemistry |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fchem.2020.00151/full |
_version_ | 1818531719679049728 |
---|---|
author | Shurui Xu Jie Wu Peng Huang Chunwen Lao Hanchao Lai Yuxiong Wang Zhenyu Wang Guoyu Zhong Xiaobo Fu Xiaobo Fu Feng Peng |
author_facet | Shurui Xu Jie Wu Peng Huang Chunwen Lao Hanchao Lai Yuxiong Wang Zhenyu Wang Guoyu Zhong Xiaobo Fu Xiaobo Fu Feng Peng |
author_sort | Shurui Xu |
collection | DOAJ |
description | In this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO3. In the reaction, the conversion rate and product selectivity could be both as high as 95% in N2 atmosphere, while the benzaldehyde yield also reached 85% in air. Similar to Fe(NO3)3·9H2O, the other metallic nitrates such as Al(NO3)3·9H2O and Cu(NO3)2·3H2O could also oxidize the benzyl alcohol with high activity. The applicability of Fe(NO3)3·9H2O for other benzylic alcohol was also investigated, and the reaction condition was optimized at the same time. The results showed the Fe(NO3)3·9H2O would be more conducive in oxidizing benzyl alcohol under the anaerobic condition. The experiments in N2 or O2 atmospheres were conducted separately to study the catalytic mechanism of Fe(NO3)3. The results showed the co-existence of Fe3+ and NO3- will generate high activity, while either was with negligible oxidation property. The cyclic transformation of Fe3+ and Fe2+ provided the catalytic action to the benzyl alcohol oxidation. The role of NO3- was also an oxidant, by providing HNO2 in anaerobic condition, while NO3- would be regenerated from NO in aerobic condition. O2 did not oxidize the benzyl alcohol conversion directly, while it could still be beneficial to the procedure by eliminating the unwelcome NO and simultaneously reinforcing the circulation of Fe2+ and Fe3+, which therefore forms a green cyclic oxidation. Hence, the benzyl alcohol oxidation was suggested in an air atmosphere for efficiency and the need of green synthesis. |
first_indexed | 2024-12-11T17:36:07Z |
format | Article |
id | doaj.art-da627b2b0a104e9796c140637974076f |
institution | Directory Open Access Journal |
issn | 2296-2646 |
language | English |
last_indexed | 2024-12-11T17:36:07Z |
publishDate | 2020-03-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Chemistry |
spelling | doaj.art-da627b2b0a104e9796c140637974076f2022-12-22T00:56:41ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462020-03-01810.3389/fchem.2020.00151525060Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by NitratesShurui Xu0Jie Wu1Peng Huang2Chunwen Lao3Hanchao Lai4Yuxiong Wang5Zhenyu Wang6Guoyu Zhong7Xiaobo Fu8Xiaobo Fu9Feng Peng10Engineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaEngineering Research Center of None-food Biomass Efficient Pyrolysis and Utilization Technology of Guangdong Higher Education Institutes, Dongguan University of Technology, Dongguan, ChinaKey Laboratory of Distributed Energy Systems of Guangdong Province, School of Chemical Engineering and Energy Technology, Dongguan University of Technology, Dongguan, ChinaGuangzhou Higher Education Mega Center, School of Chemistry and Chemical Engineering, Guangzhou University, Guangzhou, ChinaIn this paper, ferric nitrate was used to oxidize benzyl alcohol in a mild condition and demonstrated its better performance compared to HNO3. In the reaction, the conversion rate and product selectivity could be both as high as 95% in N2 atmosphere, while the benzaldehyde yield also reached 85% in air. Similar to Fe(NO3)3·9H2O, the other metallic nitrates such as Al(NO3)3·9H2O and Cu(NO3)2·3H2O could also oxidize the benzyl alcohol with high activity. The applicability of Fe(NO3)3·9H2O for other benzylic alcohol was also investigated, and the reaction condition was optimized at the same time. The results showed the Fe(NO3)3·9H2O would be more conducive in oxidizing benzyl alcohol under the anaerobic condition. The experiments in N2 or O2 atmospheres were conducted separately to study the catalytic mechanism of Fe(NO3)3. The results showed the co-existence of Fe3+ and NO3- will generate high activity, while either was with negligible oxidation property. The cyclic transformation of Fe3+ and Fe2+ provided the catalytic action to the benzyl alcohol oxidation. The role of NO3- was also an oxidant, by providing HNO2 in anaerobic condition, while NO3- would be regenerated from NO in aerobic condition. O2 did not oxidize the benzyl alcohol conversion directly, while it could still be beneficial to the procedure by eliminating the unwelcome NO and simultaneously reinforcing the circulation of Fe2+ and Fe3+, which therefore forms a green cyclic oxidation. Hence, the benzyl alcohol oxidation was suggested in an air atmosphere for efficiency and the need of green synthesis.https://www.frontiersin.org/article/10.3389/fchem.2020.00151/fullselective oxidationbenzyl alcohol oxidationgreen oxidationferric nitratecatalytic mechanism |
spellingShingle | Shurui Xu Jie Wu Peng Huang Chunwen Lao Hanchao Lai Yuxiong Wang Zhenyu Wang Guoyu Zhong Xiaobo Fu Xiaobo Fu Feng Peng Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates Frontiers in Chemistry selective oxidation benzyl alcohol oxidation green oxidation ferric nitrate catalytic mechanism |
title | Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates |
title_full | Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates |
title_fullStr | Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates |
title_full_unstemmed | Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates |
title_short | Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde by Nitrates |
title_sort | selective catalytic oxidation of benzyl alcohol to benzaldehyde by nitrates |
topic | selective oxidation benzyl alcohol oxidation green oxidation ferric nitrate catalytic mechanism |
url | https://www.frontiersin.org/article/10.3389/fchem.2020.00151/full |
work_keys_str_mv | AT shuruixu selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT jiewu selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT penghuang selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT chunwenlao selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT hanchaolai selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT yuxiongwang selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT zhenyuwang selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT guoyuzhong selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT xiaobofu selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT xiaobofu selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates AT fengpeng selectivecatalyticoxidationofbenzylalcoholtobenzaldehydebynitrates |