Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/3404
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Thangavel, Thirunavukkarasu | - |
dc.contributor.author | Eswaran, Ramachandran | - |
dc.contributor.author | Karuppannan, Natarajan | - |
dc.contributor.author | Hazel A, Sparkes | - |
dc.contributor.author | Saud I, Al-Resayes | - |
dc.contributor.author | Mohammad, Azam | - |
dc.date.accessioned | 2023-08-18T08:27:49Z | - |
dc.date.available | 2023-08-18T08:27:49Z | - |
dc.date.issued | 2023-01-15 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0277538722005599 | - |
dc.description.abstract | A novel series of stable phosphine/arsine-free Schiff base Pd(II) complexes (1–3) was synthesized and investigated using a variety of spectroscopic techniques and single crystal X-ray crystallography. A square-planar distortion was observed in all complexes centering on the Pd(II) ion. The isolated complexes (1–3) were used as catalysts for the Suzuki cross-coupling reactions in water/ethanol and water medium, resulting in good to excellent yields of the products even with a little loading of the catalyst. This methodology has the potential to be extended further to develop novel antimicrobial drugs, which can be further used in the treatment of infectious diseases. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Elsevier | en_US |
dc.title | A STUDY ON THE APPLICATIONS OF 3-AMINO QUINOLINE COMPLEXES OF PD(II) AS CATALYSTS FOR THE SUZUKI-MIYAURA COUPLING OF ARYL HALIDES IN AQUEOUS AND ORGANIC MEDIA | en_US |
dc.type | Article | en_US |
Appears in Collections: | International Journals |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
A STUDY ON THE APPLICATIONS OF 3-AMINO QUINOLINE COMPLEXES OF PD(II) AS CATALYSTS FOR THE SUZUKI-MIYAURA COUPLING OF ARYL HALIDES IN AQUEOUS AND ORGANIC MEDIA.docx | 172.88 kB | Microsoft Word XML | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.