Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/5421
Title: Studies on poly(Acrylate)s containing hydrazone ligand derived from 2,4- Dihydroxy carbonyl compounds and their divalent metal complexes
Researcher: Sankar, R
Guide(s): Kaliyappan, T
Keywords: Chemistry
Upload Date: 10-Dec-2012
University: Pondicherry University
Completed Date: February, 2008
Abstract: 2,4-dihydroxy carbonyl meth(acrylate)s hydrazones, were prepared by reacting acryloyl/methacryloyl chloride with 2,4-dihydroxy carbonyl hydrazone. 2,4-dihydroxy carbonyl hydrazone-phenol formaldehyde was prepared by condensing equimolar amount of 2,4-dihydroxy carbonyl hydrazone with formaldehyde in the presence of oxalic acid. These monomers were characterized by elemental analysis, IR and 1H-NMR spectroscopy. The monomers were polymerized in DMF medium using benzoyl peroxide as free radical initiator. The DMF solution of the polymers containing a few drops of ammonia on treatment with aqueous solution of Cu(II)/Ni(II) ions gave the corresponding metal complexes: poly(2-hydroxy- 4-acryloyloxybenzophenone hydrazone) poly(2H4ABPH)-Cu(II)/Ni(II), poly(2-hydroxy-4-methacryloyloxybenzophenone hydrazone) poly(2H4MBPH)- Cu(II)/Ni(II), poly(2-hydroxy-4 acryloyloxyacetoophenonehydrazone) poly(2H4AAPH)-Cu(II)/Ni(II), poly(2-hydroxy-4-methacryloyloxyacetoophenone) poly(2H4MAPH)-Cu(II)/Ni(II), poly(2-hydroxy-4-acryloyloxybenz aldehydehydrazone) poly(2H4ABAH)-Cu(II)/Ni(II), poly(2-hydroxy-4 methacryloyloxybenzaldehydehydrazone) poly(2H4MBAH)-Cu(II)/Ni(II) Characterization of the polymers and polymer-metal complexes were carried out. The polymers were soluble in THF, DMF, DMAc, and DMSO whereas insoluble in common organic solvents like benzene, toluene, acetone and methanol. GPC data reveals that the molecular weight W (M ) of the polymers is moderately high of the order of 3.21 × 104 - 3.94 × 104. Elemental analysis values and 1H NMR signals are in good agreement with expected structure of the polymers. The IR-spectra of polymers exhibit broad bands around 3400-3000cm-1 due to the intramolecular hydrogen bonded OH stretching,1730cm-1 due to the C=O group of ester. In the case of Cu(II) complex, the broad band is absent due to the involvement of phenolic OH group in co-ordination with the metal.
Pagination: xxii, 221p.
URI: http://hdl.handle.net/10603/5421
Appears in Departments:Department of Chemistry

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02_certificate.pdf8.56 kBAdobe PDFView/Open
03_declaration.pdf8.17 kBAdobe PDFView/Open
04_abstract.pdf37.47 kBAdobe PDFView/Open
05_acknowledgements.pdf11.18 kBAdobe PDFView/Open
06_table of contents.pdf16.15 kBAdobe PDFView/Open
07_list of tables.pdf14.96 kBAdobe PDFView/Open
08_list of figures.pdf22.38 kBAdobe PDFView/Open
09_list of abbreviations.pdf46.65 kBAdobe PDFView/Open
10_dedication.pdf303.77 kBAdobe PDFView/Open
11_chapter 1.pdf961.73 kBAdobe PDFView/Open
12_chapter 2.pdf62.86 kBAdobe PDFView/Open
13_chapter 3.pdf5.15 MBAdobe PDFView/Open
14_chapter 4.pdf23.12 kBAdobe PDFView/Open
15_references.pdf37.47 kBAdobe PDFView/Open
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