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Cost‐effective bio‐derived mesoporous carbon nanoparticles‐supported palladium catalyst for nitroarene reduction and Suzuki–Miyaura coupling by microwave approach
Author(s) -
Supriya S.,
Ananthnag Guddekoppa S.,
Shetti Vijayendra S.,
Nagaraja B.M.,
Hegde Gurumurthy
Publication year - 2020
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5384
Subject(s) - chemistry , catalysis , palladium , heterogeneous catalysis , mesoporous material , aryl , suzuki reaction , boronic acid , combinatorial chemistry , nuclear chemistry , organic chemistry , alkyl
A new heterogeneous catalyst was synthesized by immobilizing Pd on areca nut kernel‐derived carbon nanospheres (CNSs). The CNSs, without any further activation processes, accommodated 3% of Pd on their surface. The new Pd/CNS material was used for the reduction of nitroarenes and Suzuki–Miyaura coupling of bromoarenes with aryl boronic acids. The reactions were conducted under microwave irradiation at 160 °C using 12 mol% of Pd/CNS (0.36% actual Pd content). The reduction of nitroarenes into their respective amino compounds was achieved in 10–20 min (conversion up to 100%); by contrast, the Suzuki–Miyaura reactions yielded up to 98% at 150 °C with 10 mol% of Pd/CNS catalyst. The products were identified using gas chromatography and nuclear magnetic resonance spectroscopy. The catalyst was isolated from reaction mixture and reused without any significant loss in the activity. Thus, the present work introduces one‐pot‐derived porous CNSs as efficient catalytic support to Pd, establishing an alternative to existing Pd/C in terms of cost and efficiency.