Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/577514
Full metadata record
DC FieldValueLanguage
dc.coverage.spatial
dc.date.accessioned2024-07-19T11:32:14Z-
dc.date.available2024-07-19T11:32:14Z-
dc.identifier.urihttp://hdl.handle.net/10603/577514-
dc.description.abstractElectro-organic synthesis has gained widespread attention due to the advantages such as green catalyst, atom economy, good selectivity and excellent yields. The use of newlinetailor-made modified electrodes helps in refining the electronic and surface properties which could be harnessed for synthesis of important heterocyclic and carbocyclic motifs. The fabrication of modified electrode is done by employing a carbon fiber paper substrate as the base followed by electropolymerization of a desired monomer. The functional group in the monomer is utilized for covalently immobilizing the desired catalyst such as enzyme, organometallic, transition-metal and organocatalyst over the electrode. The developed electrocatalyst is employed in the electrochemical synthesis of heterocyclic and carbocyclic motifs. The electrochemical characterization studies for the electrodes were determined using electrochemical active surface area, electrochemical impedance spectroscopy and electron transfer kinetics studies. The surface morphology of the fabricated electrode was differentiated in contrast to the other electrode by utilizing Scanning electron microscopy (SEM) and Optical Profilometry (OP). The other characterization of the electrode includes X-ray photoelectron spectroscopy (XPS), Fourier Transform Infrared (FT-IR) analysis for the newlinestructural confirmations. The fabricated modified electrode was then employed for the newlineelectrochemical organic transformation by carrying out several optimization reactions. newlineThe screening studies was carried out by employing different supporting electrolyte, newlinesolvents and electrochemical studies. The completion of the electrochemical organic newlinesynthesis was observed by Thin-layer chromatography (TLC) and desired product was newlineisolated either using column chromatography or just by solvent evaporation after newlineworkup.
dc.format.extentxx, 167p.;
dc.languageEnglish
dc.relation270
dc.rightsuniversity
dc.titleElectrochemical synthesis of carbocyclic and heterocyclic motifs
dc.title.alternative
dc.creator.researcherThadathil, Ditto Abraham
dc.subject.keywordAnchored Organocatalyst.
dc.subject.keywordAnchored Organometal,
dc.subject.keywordAnchored Transition-Metal,
dc.subject.keywordBioenzymatic,
dc.subject.keywordCarbon Fiber Paper,
dc.subject.keywordChemistry
dc.subject.keywordElectrocatalysis,
dc.subject.keywordElectrochemistry
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideVarghese, Anitha
dc.publisher.placeBangalore
dc.publisher.universityCHRIST University
dc.publisher.institutionDepartment of Chemistry
dc.date.registered2021
dc.date.completed2024
dc.date.awarded2024
dc.format.dimensionsA4
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File176.31 kBAdobe PDFView/Open
02_prelim pages.pdf832.7 kBAdobe PDFView/Open
03_abstract.pdf15.96 kBAdobe PDFView/Open
04_table_of_contents.pdf37.86 kBAdobe PDFView/Open
05_chapter1.pdf441.56 kBAdobe PDFView/Open
06_chapter2.pdf272.4 kBAdobe PDFView/Open
07_chapter3.pdf1.16 MBAdobe PDFView/Open
08_chapter4.pdf1 MBAdobe PDFView/Open
09_chapter5.pdf721.62 kBAdobe PDFView/Open
10_chapter6.pdf773.35 kBAdobe PDFView/Open
11_chapter7.pdf83.89 kBAdobe PDFView/Open
12_annexures.pdf72.58 kBAdobe PDFView/Open
80_recommendation.pdf259.51 kBAdobe PDFView/Open


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: