پديدآورندگان :
Irani Mahsa Urmia University , Hasanzadeh Reza Urmia University , Najafi Moghadam Peyman p_najafi27@yahoo.com Urmia University
چكيده فارسي :
Polymeric macromonomers are containing one or more polymerizablefunctional groups,
which are typically located at the chain end(s) or side chain. They can be polymerized with
low molecular weight monomers to generate brush-like [1] and complex structures such as
graft copolymers, star polymers, and dendronized polymers [2]. Generally, two synthetic
strategies have been used to prepare near monodispersemacromonomers: a) direct synthesis of
macromonomers using a vinyl-functional initiator that does not participate in the chaingrowth
reaction and b) preparation of end-functionalized polymers, followed by postpolymerization
modification [2]. Until recently, however, these polymers have been prepared
through polymerization them by free-radical polymerization processes [3].
In this work a bio-macromonomer was synthesized by reaction of Glycidylmethacrylate
(GMA) and polyvinylalcohol (PVA) in N-Methyl-2-pyrrolidone (NMP) as solvent. For this
purposePVA was resolved in the solvent and then GMA was added to the solution mixture
and the reaction was carried out for 24hr at room temperature under Ar atmosphere. After
completion of the reaction the product was precipitated in methanol as nonsolvent and washed
with ether several times.The macromonomer was characterized with Fourier transfer infrared
spectroscopy (FT-IR),1HNMR,13C NMR, TGA and SEM analysis.