Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/15834
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dc.coverage.spatialChemistryen_US
dc.date.accessioned2014-02-12T09:16:03Z-
dc.date.available2014-02-12T09:16:03Z-
dc.date.issued2014-02-12-
dc.identifier.urihttp://hdl.handle.net/10603/15834-
dc.description.abstractAn attempt to design imprinted polymers for the specific and selective newlinerecognition of Boc-L-tryptophan, Boc-L-phenylalanine and D-mandelic acid is newlinepresented in this thesis. Emphasis is given to the tailoring of imprinted newlinepolymers for these templates with maximum specificity and selectivity. Basic newlinefunctional monomer 4-vinylpyridine (4-VP), which is an electrophilic newlinemonomer was utilized for the preparation of imprinted polymers for these newlinetemplates with a carboxyl group in the molecule. Crosslinkers namely ethylene newlineglycol dimethacrylate (EGDMA) and divinylbenzene (DVB) with widely newlinevarying degree of rigidity, flexibility and polarity were selected as crosslinking newlineagents for evaluating the nature and degree of crosslinking and for optimizing newlinethe conditions for maximum specificity and selectivity of imprinted polymers. newlineSpectroscopic methods such as Fourier-transform infra-red (FT-IR), UV-vis, newlineNMR and fluorescence technique have been used for the investigation of newlineinteraction between template and functional monomer. Scanning electron newlinemicroscopy gave the surface morphological differences between imprinted and newlinenon-imprinted polymers. The binding studies and the selectivity of the newlinepolymers were analyzed using UV-vis spectrophotometer. The polymer newlinepreparations were evaluated and compared with non-imprinted polymers for newlinetheir ability to bind the print molecule which is a measure of the specificity of newlinethe imprinted system. The binding of other substrates similar in structure to the newlineprint molecule was also analyzed to monitor the selectivity of the imprinted newlinesystem and the selectivity of the imprinted polymers was quantified as newlineseparation and selectivity factors. Significant cross reactivity was observed and newlinethe nature of the Scatchard plots was a direct indication of binding site newlineheterogeneity. The nature and degree of crosslinking and other parameters like newlineconcentration of the template solution, mass of the polymer, solvent, time and newlinethe ratio between functional monomer and template which influences the newlinebindingen_US
dc.format.extent193p.en_US
dc.languageEnglishen_US
dc.relation-en_US
dc.rightsuniversityen_US
dc.titleDesign of molecular imprinted polymers with selectivity towards Amino acidsen_US
dc.title.alternative-en_US
dc.creator.researcherThomas, Ansammaen_US
dc.subject.keywordChemistryen_US
dc.subject.keywordpolymersen_US
dc.subject.keywordAmino acidsen_US
dc.description.noteReferences given chapter wiseen_US
dc.contributor.guideMathew, Beenaen_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.completed2010en_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 File15.26 kBAdobe PDFView/Open
02_dedication.pdf22.71 kBAdobe PDFView/Open
03_declaration.pdf63.29 kBAdobe PDFView/Open
04_certificate.pdf84.37 kBAdobe PDFView/Open
05_acknowledgements.pdf54.78 kBAdobe PDFView/Open
06_abstract.pdf16.87 kBAdobe PDFView/Open
07_preface.pdf64.6 kBAdobe PDFView/Open
08_contents.pdf120.98 kBAdobe PDFView/Open
09_list of tables.pdf25.66 kBAdobe PDFView/Open
10_list of figures.pdf73.61 kBAdobe PDFView/Open
11_list of schemes.pdf13.29 kBAdobe PDFView/Open
12_list of abbreviations.pdf62.88 kBAdobe PDFView/Open
13_chapter 1.pdf215.57 kBAdobe PDFView/Open
14_chapter 2.pdf595.68 kBAdobe PDFView/Open
15_chapter 3.pdf395.03 kBAdobe PDFView/Open
16_chapter 4.pdf2.34 MBAdobe PDFView/Open
17_chapter 5.pdf206.14 kBAdobe PDFView/Open


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