A palladium nanoparticle-catalyzed aryl-amine coupling reaction: High performance of aryl and pyridyl chlorides as the coupling partner

Debkumar Nandi; Rafique Ul Islam; Nishu Devi; Samarjeet Siwal; Kaushik Mallick

doi:10.1039/c7nj03447d

A palladium nanoparticle-catalyzed aryl-amine coupling reaction: High performance of aryl and pyridyl chlorides as the coupling partner

Debkumar Nandi, Rafique Ul Islam, Nishu Devi, Samarjeet Siwal, Kaushik Mallick

Chemical Sciences

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

Abstract

Carbon nitride (CN)-supported nanosized palladium particles, Pd-CN, have been found to be an active catalyst system for the amination of aryl and pyridyl chloride moieties in the presence of dialkyl amine under mild reaction conditions. The recyclability study of the reaction shows the stable performance of the catalyst without a significant loss of catalytic activity for a couple of cycles.

Original language	English
Pages (from-to)	812-816
Number of pages	5
Journal	New Journal of Chemistry
Volume	42
Issue number	2
DOIs	https://doi.org/10.1039/c7nj03447d
Publication status	Published - 2018

ASJC Scopus subject areas

Catalysis
General Chemistry
Materials Chemistry

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abstract = "Carbon nitride (CN)-supported nanosized palladium particles, Pd-CN, have been found to be an active catalyst system for the amination of aryl and pyridyl chloride moieties in the presence of dialkyl amine under mild reaction conditions. The recyclability study of the reaction shows the stable performance of the catalyst without a significant loss of catalytic activity for a couple of cycles.",

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AU - Islam, Rafique Ul

AU - Devi, Nishu

AU - Siwal, Samarjeet

AU - Mallick, Kaushik

PY - 2018

Y1 - 2018

N2 - Carbon nitride (CN)-supported nanosized palladium particles, Pd-CN, have been found to be an active catalyst system for the amination of aryl and pyridyl chloride moieties in the presence of dialkyl amine under mild reaction conditions. The recyclability study of the reaction shows the stable performance of the catalyst without a significant loss of catalytic activity for a couple of cycles.

AB - Carbon nitride (CN)-supported nanosized palladium particles, Pd-CN, have been found to be an active catalyst system for the amination of aryl and pyridyl chloride moieties in the presence of dialkyl amine under mild reaction conditions. The recyclability study of the reaction shows the stable performance of the catalyst without a significant loss of catalytic activity for a couple of cycles.

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A palladium nanoparticle-catalyzed aryl-amine coupling reaction: High performance of aryl and pyridyl chlorides as the coupling partner

Abstract

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