Synthesis of Bis (n-salicylidene-n-phenyl aminato) Palladium (II) complex to prepare a number of biphenyl compounds

Authors

  • Md A Hashem Department of Chemistry, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
  • SK Tuli Department of Chemistry, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh
  • TB Mahmud Department of Chemistry, Jahangirnagar University, Savar, Dhaka-1342, Bangladesh

DOI:

https://doi.org/10.3329/bjsir.v54i3.42674

Keywords:

Catalysis; Non-toxic palladium complex; Coupling reaction; Phenyl boronic acid

Abstract

The non-toxic, stable, Schiff base complex of Na2PdCl4 and N-salicylidene-N-phenyl amine in methanol catalyze the Suzuki-Miyaura coupling reaction to synthesize coupling products (Scheme-1) in good to excellent yields with high purity under mild conditions.

212222.jpg

Bangladesh J. Sci. Ind. Res.54(3), 223-230, 2019

Downloads

Download data is not yet available.
Abstract
18
PDF
27

Downloads

Published

2019-08-19

How to Cite

Hashem, M. A., Tuli, S., & Mahmud, T. (2019). Synthesis of Bis (n-salicylidene-n-phenyl aminato) Palladium (II) complex to prepare a number of biphenyl compounds. Bangladesh Journal of Scientific and Industrial Research, 54(3), 223–230. https://doi.org/10.3329/bjsir.v54i3.42674

Issue

Vol. 54 No. 3 (2019)

Section

Articles

License

Bangladesh Council of Scientific and Industrial Research (BCSIR) holds the copyright to all contents published in Bangladesh Journal of Scientific and Industrial Research (BJSIR). A copyright transfer form should be signed by the author(s) and be returned to BJSIR.

The entire contents of the BJSIR are protected under Bangladesh Council of Scientific and Industrial Research (BCSIR) copyrights.

Creative Commons Licence
BJSIR is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC) Creative Commons Attribution-NonCommercial 4.0 International License which allows others remix, tweak, and build upon the articles non-commercially, and although their new works must also acknowledge and be non-commercial, they don’t have to license their derivative works on the same terms.