Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/6773
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dc.coverage.spatialChemistryen_US
dc.date.accessioned2013-01-28T04:47:53Z-
dc.date.available2013-01-28T04:47:53Z-
dc.date.issued2013-01-28-
dc.identifier.urihttp://hdl.handle.net/10603/6773-
dc.description.abstractFive novel gas-phase cyclisation reactions of suitably substituted aromatic compounds upon protonation by fast atom bombardment (FAB), chemical ionization (CI) and electrospray ionisation (ESI) in mass spectrometry have been explored. The [M+H]+ ions of N- [2-(benzoyloxy) phenyl]-benzamide eliminates benzoic acid with concomitant cyclisation, producing protonated 2-phenylbenzoxazole. A novel electrophilic cyclisation utilizing the protonated nitro group as electrophile, followed by competitive eliminations of two OH radicals and H2O from the [M+H]+ ions of 2-nitrophenyl phenyl ether afford heterocyclic product ions. Analogous cyclization of protonated 2-nitro-N phenylaniline followed by eliminations of H2O and OH radical yield heterocyclic fragments. The protonated 2-nitrophenyl-phenyl sulfide also undergoes cyclisation in gas-phase analogous to 2-nitrophenyl-phenyl ether. In addition, a novel ortho effect of nitro group involving cyclisations due to oxygen transfers from the nitro group to the sulphur atom occurs in protonated 2-nitrophenyl phenyl sulfide which resulted in the expulsions of SO and SO2 loss. Moreover, the sulfide undergoes oxidation at the emitter electrode in the ESI source during ionization in acidic solution. The mechanisms proposed for each cyclisation was supported by high-resolution data, chemical substitution, deuterium-labeling, tandem mass spectrometry experiments and theoretical calculations by density functional theory.en_US
dc.format.extent229p.en_US
dc.languageEnglishen_US
dc.relation-en_US
dc.rightsuniversityen_US
dc.titleGas phase intramolecular cyclisation reactions of ionized aromatic compounds in mass spectrometryen_US
dc.title.alternative-en_US
dc.creator.researcherMoolayil, Joseph Ten_US
dc.subject.keywordortho effecten_US
dc.subject.keywordChemistryen_US
dc.subject.keywordcyclisationen_US
dc.subject.keywordmass spectrumen_US
dc.subject.keywordfast atom bombardmenten_US
dc.subject.keywordmass spectrometryen_US
dc.subject.keywordChemical ionizationen_US
dc.subject.keywordElectrospray ionisationen_US
dc.subject.keywordcollision-induced dissociationen_US
dc.subject.keywordMetastable ionen_US
dc.description.noteReferences given chapters wiseen_US
dc.contributor.guideGeorge, Men_US
dc.publisher.placeKottayamen_US
dc.publisher.universityMahatma Gandhi Universityen_US
dc.publisher.institutionSchool Of Chemical Sciencesen_US
dc.date.registeredn.d.en_US
dc.date.completedFebruary, 2007en_US
dc.date.awardedn.d.en_US
dc.format.dimensions-en_US
dc.format.accompanyingmaterialNoneen_US
dc.type.degreePh.D.en_US
dc.source.inflibnetINFLIBNETen_US
Appears in Departments:School Of Chemical Science

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01_title.pdfAttached File31.44 kBAdobe PDFView/Open
02_dedication.pdf33.01 kBAdobe PDFView/Open
03_declaration.pdf70.65 kBAdobe PDFView/Open
04_certificate.pdf50.3 kBAdobe PDFView/Open
05_acknowledgements.pdf78.66 kBAdobe PDFView/Open
06_abstract.pdf46.51 kBAdobe PDFView/Open
07_preface.pdf39.87 kBAdobe PDFView/Open
08_contents.pdf51.4 kBAdobe PDFView/Open
09_list of abbreviations.pdf37.94 kBAdobe PDFView/Open
10_list of tables.pdf54.13 kBAdobe PDFView/Open
11_list of figures.pdf111.32 kBAdobe PDFView/Open
12_chapter 1.pdf437.47 kBAdobe PDFView/Open
13_chapter 2.pdf613.57 kBAdobe PDFView/Open
14_chapter 3.pdf1 MBAdobe PDFView/Open
15_chapter 4.pdf707.31 kBAdobe PDFView/Open
16_chapter 5.pdf568.52 kBAdobe PDFView/Open
17_chapter 6.pdf58.8 kBAdobe PDFView/Open
18_summary.pdf86.05 kBAdobe PDFView/Open
19_list of publications.pdf44.48 kBAdobe PDFView/Open


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