Differences in the selective reduction mechanism of 4-nitroacetophenone catalysed by rutile- and anatase-supported ruthenium catalysts. Issue 5 (5th February 2020)
- Record Type:
- Journal Article
- Title:
- Differences in the selective reduction mechanism of 4-nitroacetophenone catalysed by rutile- and anatase-supported ruthenium catalysts. Issue 5 (5th February 2020)
- Main Title:
- Differences in the selective reduction mechanism of 4-nitroacetophenone catalysed by rutile- and anatase-supported ruthenium catalysts
- Authors:
- Zhang, Jin
Pei, Linjuan
Wang, Jie
Zhu, Pengqi
Gu, Xianmo
Zheng, Zhanfeng - Abstract:
- Abstract : Ru nanoparticles supported on different crystalline TiO2 (anatase and rutile) phases result in different reaction pathways for 4-nitroacetophenone. Abstract : Ru/TiO2 catalysts exhibit excellent catalytic performance for selective reduction of 4-nitroacetophenone to 4-aminoacetophenone at normal temperature and atmospheric hydrogen pressure. Moreover, 99.9% selectivity to 4-aminoacetophenone can be obtained over 2.7 wt% Ru/TiO2 (anatase) catalyst even in a relatively wide temperature (55–115 °C) and time (1–12 h) range. Its excellent catalytic performance is derived from the activation of H2 on the Ru nanoparticles at atmospheric pressure and the strong interaction of nitro groups with the support surface. Additionally, Ru nanoparticles supported on different crystalline TiO2 phases (anatase and rutile) result in different reaction pathways for 4-nitroacetophenone. Since the Ti–Ti distance on the rutile surface is smaller than that on the anatase surface, the hydroxylamine species adsorbed on the Ti atoms of rutile are more susceptible to the coupling reaction. Therefore, Ru/TiO2 (rutile) causes a series of intermediates to accumulate during the conversion process, while Ru/TiO2 (anatase) allows the highly selective conversion of 4-nitroacetophenone to 4-aminophenone. In addition, Ru/TiO2 (anatase) can achieve chemoselective reduction of nitroaromatics to the corresponding anilines in the presence of –CN, –CHO, and –COOH, especially nitroaromatics containing CCAbstract : Ru nanoparticles supported on different crystalline TiO2 (anatase and rutile) phases result in different reaction pathways for 4-nitroacetophenone. Abstract : Ru/TiO2 catalysts exhibit excellent catalytic performance for selective reduction of 4-nitroacetophenone to 4-aminoacetophenone at normal temperature and atmospheric hydrogen pressure. Moreover, 99.9% selectivity to 4-aminoacetophenone can be obtained over 2.7 wt% Ru/TiO2 (anatase) catalyst even in a relatively wide temperature (55–115 °C) and time (1–12 h) range. Its excellent catalytic performance is derived from the activation of H2 on the Ru nanoparticles at atmospheric pressure and the strong interaction of nitro groups with the support surface. Additionally, Ru nanoparticles supported on different crystalline TiO2 phases (anatase and rutile) result in different reaction pathways for 4-nitroacetophenone. Since the Ti–Ti distance on the rutile surface is smaller than that on the anatase surface, the hydroxylamine species adsorbed on the Ti atoms of rutile are more susceptible to the coupling reaction. Therefore, Ru/TiO2 (rutile) causes a series of intermediates to accumulate during the conversion process, while Ru/TiO2 (anatase) allows the highly selective conversion of 4-nitroacetophenone to 4-aminophenone. In addition, Ru/TiO2 (anatase) can achieve chemoselective reduction of nitroaromatics to the corresponding anilines in the presence of –CN, –CHO, and –COOH, especially nitroaromatics containing CC and CC, indicating the excellent applicability. … (more)
- Is Part Of:
- Catalysis science & technology. Volume 10:Issue 5(2020)
- Journal:
- Catalysis science & technology
- Issue:
- Volume 10:Issue 5(2020)
- Issue Display:
- Volume 10, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 10
- Issue:
- 5
- Issue Sort Value:
- 2020-0010-0005-0000
- Page Start:
- 1518
- Page End:
- 1528
- Publication Date:
- 2020-02-05
- Subjects:
- Catalysis -- Periodicals
541.395 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/CY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cy02260k ↗
- Languages:
- English
- ISSNs:
- 2044-4753
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3090.943100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13855.xml