Highly efficient and selective reduction of nitroarenes into anilines catalyzed by gold nanoparticles incarcerated in a nanoporous polymer matrix: Role of the polymeric support and insight into the reaction mechanism

2016 ◽  
Vol 340 ◽  
pp. 30-40 ◽  
Author(s):  
Annarita Noschese ◽  
Antonio Buonerba ◽  
Patrizia Canton ◽  
Stefano Milione ◽  
Carmine Capacchione ◽  
...  
2015 ◽  
Vol 17 (16) ◽  
pp. 10391-10397 ◽  
Author(s):  
Alexander Lüken ◽  
Martin Muhler ◽  
Jennifer Strunk

Partial insight into the reaction mechanism of the photooxidation of 2-propanol over Au/TiO2. 2-Propanol is activated by hole capture and converted to acetone requiring the presence of O2 as an electron acceptor. The deposited Au nanoparticles are assumed to facilitate the electron transfer from the TiO2 conduction band to adsorbed O2.


Small ◽  
2014 ◽  
Vol 10 (22) ◽  
pp. 4664-4670 ◽  
Author(s):  
Xiang Ma ◽  
Kun Zhao ◽  
Hongjie Tang ◽  
Ying Chen ◽  
Chenguang Lu ◽  
...  

2022 ◽  
Vol 8 ◽  
pp. 37-44
Author(s):  
Zhanwu Wang ◽  
Wenjie He ◽  
Meiling Ma ◽  
Yingrui Sui

Author(s):  
Muhammad Irfan ◽  
Muhammad Moniruzzaman ◽  
Tausif Ahmad ◽  
Mohamad Fakhrul Ridhwan Samsudin ◽  
Farzana Bashir ◽  
...  

2018 ◽  
Vol 15 (5) ◽  
pp. 578-586 ◽  
Author(s):  
Avtar Singh ◽  
Nirmaljeet Kaur ◽  
Harish Kumar Chopra

Background: Enantioselective reduction reactions play a key role to synthesize compounds of industrial importance. A number of metal and biocatalysts have been developed for their use in this reaction. Chiral ionic liquids (CILs) have been widely used as the reaction medium and the organocatalysts in enantioselective reduction reactions. Objective: This paper focuses on the systematic literature review about the use of chiral ionic liquids (CILs) in the enantioselective reduction reaction. The mechanistic aspects of these species are also taken into account. Conclusion: This review concludes that a number of chiral ionic liquids (CILs) have been successfully employed as the organocatalysts and the reaction medium in the enantioselective reduction reactions. The review also gives an insight into the role of these species in the reaction mechanism. For most of the reactions, chiral ionic liquids provide promising results in terms of yield and enantioselectivity. The recyclability of these chiral moieties from the reaction mixtures offers an additional benefit for the use of these species in asymmetric reactions.


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