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dc.contributor Assoc. Prof. Program in Chemistry.
dc.contributor.author Küsefoğlu, Selim.
dc.date.accessioned 2023-03-16T13:19:54Z
dc.date.available 2023-03-16T13:19:54Z
dc.date.issued 1980.
dc.identifier.other CHEM 1980 K968 Doc
dc.identifier.uri http://digitalarchive.boun.edu.tr/handle/123456789/19154
dc.description.abstract The known and varied organic chemistry o f the furan ring has been used t o successfully transform poly-2-vinyl furan (PZVF) to a number of new polymeric systems. The Diels Alder adduct o f P2VF with maleicanhidride (3), the cross linking product of P2VF with asetone (7); the 2 - 4 dinitroph,enylhydrazine derivative of the acid hydrolysis product of P2VF (6) and the 5-aldehyde (8), 5-bromide (9) and 5-sulfonat (10) derivatives of P2VF have been synthesized and characterized using spectral and chemical techniques. The spectral and chemical properties o f the starting material P2VF which were not available in the literature have also been determined. Each o f the above syntheses involved the limitations and difficulties inherent in polymer reactions which had to be eliminated or minimized by judicial use of synthesis techniques. Although the physical propertiies o f the newly synthesized polymers lies outside the scope of this work, especially the P2VF maleican hidrite Diels-Alder adduct (3) and P2VF - asetone cross-linking product (7) deserve careful physical tests for further characterization.
dc.format.extent 30 cm.
dc.publisher Thesis (Assoc. Prof.) - Bogazici University. Institute for Graduate Studies in Science and Engineering, 1980.
dc.relation Includes appendices.
dc.relation Includes appendices.
dc.subject.lcsh Chemistry, Organic.
dc.subject.lcsh Heterocyclic compounds.
dc.title Poli-2-vinilfuran'ın organik reaksiyonları
dc.format.pages vi, 83 leaves;


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