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Title: | DESIGN AND SYNTHESIS OF BASE-METAL COORDINATION COMPLEXES AND THEIR APPLICATIONS AS CATALYSTS IN DIFFERENT ORGANIC TRANSFORMATIONS |
Authors: | Singh, Anshu |
Keywords: | Manganese, Iron, Cobalt, Nickel and Copper Complexes;Copper-based Catalysts;N-alkylation of Amines;-alkylation of Ketones and Synthesis of Quinolines |
Issue Date: | Jul-2021 |
Publisher: | IIT Roorkee |
Abstract: | The thesis entitled “Design and Synthesis of Base-metal Coordination Complexes and their Applications as Catalysts in Different Organic Transformations” is reported in seven chapters. In the present work is aimed to design and synthesis of unsymmetrical salen-type ligands, pentadentate ligands, pincer-ligands and azo-based non-innocent ligands. These ligands were characterized through different analytical techniques such as UV-visible, IR, NMR, ESIMS and NMR spectroscopy. These ligands were utilized for the synthesis of manganese, iron, cobalt, nickel and copper complexes. These synthesized complexes were characterized by UVvisible, IR, NMR, ESI-MS spectroscopy. Complexes were characterized by X-ray crystallography. These complexes were utilized as catalysts for different organic transformation involving C−C, C−N bonds formation using different reactions like synthesis of tetrazoles and propargylamines, reduction of nitroaromatics, N‐alkylation and α‐alkylation of ketones with alcohols and synthesis of quinolines, quinazoline and quinazoli-4(3H)-ones. We have done the selective dimerization of ethylene to 1-butene using diethyl aluminium chloride (DEAC) as a co-catalyst. The synthesized compounds were characterized through different analytical techniques such as NMR analysis. We have also done some biological activity such as superoxide dismutase activity. |
URI: | http://localhost:8081/jspui/handle/123456789/18025 |
Research Supervisor/ Guide: | Ghosh, Kaushik |
metadata.dc.type: | Thesis |
Appears in Collections: | DOCTORAL THESES (chemistry) |
Files in This Item:
File | Description | Size | Format | |
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ANSHU SINGH 15909018.pdf | 23.91 MB | Adobe PDF | View/Open |
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