Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/462848
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dc.date.accessioned2023-02-18T10:42:25Z-
dc.date.available2023-02-18T10:42:25Z-
dc.identifier.urihttp://hdl.handle.net/10603/462848-
dc.description.abstractSchiff bases represent a class of organic compounds which are formed by condensing primary amines with carbonyl compounds giving rise to CH=N- functional group. They behave like ligands during complexation processes and at the same time can act as materials for semiconducting, optical as well as therapeutic activities. The present work embodies the synthesis and characterization of some 4-aminoantipyrine (4-AAP) based Schiff bases. It is well known that antipyrine derivatives are used in various pharmaceutical industries as they have analgesic, antitumor, antimicrobial, antiviral and anti-inflammatory properties.
dc.format.extent
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleCorrosion Inhibition and Solvent Polarity Impacts of Some 4 Aminoantipyrine Based Schiff Base Ligands
dc.title.alternative
dc.creator.researcherUpadhyay, Ankita
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideKar, Pravin Kumar and Dash, Sukalyan
dc.publisher.placeSambalpur
dc.publisher.universityVeer Surendra Sai University of Technology
dc.publisher.institutionDepartment of Chemistry
dc.date.registered2015
dc.date.completed2021
dc.date.awarded2021
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

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01_title.pdfAttached File77.98 kBAdobe PDFView/Open
02_prelim pages.pdf1.13 MBAdobe PDFView/Open
03_contents.pdf445.4 kBAdobe PDFView/Open
04_abstract.pdf99.36 kBAdobe PDFView/Open
05_chapter 1.pdf473.7 kBAdobe PDFView/Open
06_chapter 2.pdf900.26 kBAdobe PDFView/Open
07_chapter 3.pdf1.09 MBAdobe PDFView/Open
08_chapter 4.pdf852.29 kBAdobe PDFView/Open
09_chapter 5.pdf2.25 MBAdobe PDFView/Open
10_chapter 6.pdf1.1 MBAdobe PDFView/Open
11_chapter 7.pdf987.28 kBAdobe PDFView/Open
12_chapter 8.pdf469.31 kBAdobe PDFView/Open
13_annexure.pdf1.55 MBAdobe PDFView/Open
80_recommendation.pdf546.65 kBAdobe PDFView/Open


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