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Facile synthesis of controllable graphene-co-shelled reusable Ni/NiO nanoparticles and their application in the synthesis of amines under mild conditions.

Authors :
Liu, Jianguo
Zhu, Yuting
Wang, Chenguang
Singh, Thishana
Wang, Nan
Liu, Qiying
Cui, Zhibing
Ma, Longlong
Source :
Green Chemistry; 11/7/2020, Vol. 22 Issue 21, p7387-7397, 11p
Publication Year :
2020

Abstract

The primary objective of many researchers in chemical synthesis is the development of recyclable and easily accessible catalysts. These catalysts should preferably be made from Earth-abundant metals and have the ability to be utilised in the synthesis of pharmaceutically important compounds. Amines are classified as privileged compounds, and are used extensively in the fine and bulk chemical industries, as well as in pharmaceutical and materials research. In many laboratories and in industry, transition metal catalysed reductive amination of carbonyl compounds is performed using predominantly ammonia and H<subscript>2</subscript>. However, these reactions usually require precious metal-based catalysts or RANEY® nickel, and require harsh reaction conditions and yield low selectivity for the desired products. Herein, we describe a simple and environmentally friendly method for the preparation of thin graphene spheres that encapsulate uniform Ni/NiO nanoalloy catalysts (Ni/NiO@C) using nickel citrate as the precursor. The resulting catalysts are stable and reusable and were successfully used for the synthesis of primary, secondary, tertiary, and N-methylamines (more than 62 examples). The reaction couples easily accessible carbonyl compounds (aldehydes and ketones) with ammonia, amines, and H<subscript>2</subscript> under very mild industrially viable and scalable conditions (80 °C and 1 MPa H<subscript>2</subscript> pressure, 4 h), offering cost-effective access to numerous functionalized, structurally diverse linear and branched benzylic, heterocyclic, and aliphatic amines including drugs and steroid derivatives. We have also demonstrated the scale-up of the heterogeneous amination protocol to gram-scale synthesis. Furthermore, the catalyst can be immobilized on a magnetic stirring bar and be conveniently recycled up to five times without any significant loss of catalytic activity and selectivity for the product. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14639262
Volume :
22
Issue :
21
Database :
Complementary Index
Journal :
Green Chemistry
Publication Type :
Academic Journal
Accession number :
146791526
Full Text :
https://doi.org/10.1039/d0gc02421j