2012
DOI: 10.4236/ojpchem.2012.22006
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Synthesis and Characterization of Lactone Functional Macromonomers by End Group Deactivation and Their Use in Miktoarm Star Polymer

Abstract: Newly designed miktoarm star-shaped copolymers made of poly[(benzyl methacrylate(BMA)-co-(-caprolacton)(CL)] and poly[(BMA-b-MMA-b-BMA)-co--caprolacton)(CL)] were synthesized by combining ring-opening polymerization (ROP) of -caprolactone (CL) and poly(BMA) five membered lacton fuctionalized prepared via atom transfer radical polymerization (ATRP) of BMA, and -CL and P(BMA-b-MMA-b-BMA) dual functionalized diblock copolymer, in the presence of tin(II) bis(2-ethylhexanoate) (Sn(Oct) 2 ). Although lactone end… Show more

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Cited by 6 publications
(6 citation statements)
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“…Ethyl alcohol was obtained from Fluka. 4‐Chloromethyl‐7‐hydroxycoumarone was obtained from our previous study …”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Ethyl alcohol was obtained from Fluka. 4‐Chloromethyl‐7‐hydroxycoumarone was obtained from our previous study …”
Section: Methodsmentioning
confidence: 99%
“…The synthesis of 4‐chloromethyl‐7‐methacryloyloxy coumarone (ClMMAOC) monomer is carried out in accordance with the standard method and our previous study . The monomer was synthesized by the reaction of 4‐chloromethyl‐7‐hydroxycoumarone and methacryloyl chloride at 0–5°C by using TEA.…”
Section: Methodsmentioning
confidence: 99%
“…The resulting product, 7-hydroxyl-4-chloro-methyl coumarone, was recovered by filtration and then cleansed with the use of 9:1 n-hexane/ethyl acetate as an eluent. 1 H-NMR (␦, ppm): 4.89 (2H, CI-CH 2 -), 6.40 (1H, olefinic proton on coumarone), 6.79 and 6.91 (protons on 5 and 6 carbons in aromatic ring), 7.71 (1H, between two rings coumarone unities) (Demirelli and Bezgin, 2012).…”
Section: Pigment and Resin Technologymentioning
confidence: 99%
“…Carbon-13 ( 13 C)-NMR (␦, ppm): 41.3 (CI-CH 2 -), 126.2, 112.9, 111.6, 110.1, 102.8 (carbons with hydrogen of coumarone) (Demirelli and Bezgin, 2012).…”
Section: Pigment and Resin Technologymentioning
confidence: 99%
“…Block copolymers containing PDEAEMA blocks are widely used in the literature as pH -and temperature responsive materials in aqueous solutions, as a consequence of the increase in hydrophobicity upon deprotonation [19,20]. On the other hand benzyl methacrylate (BzMA) is a very interesting monomer, which can be used as a substitute in the methacrylate family of monomers of the very commonly used styrene (St) in copolymerization studies [21]. PBzMA is also hydrophobic and amorphous as PSt but with a much lower glass transition, Tg, value [(Tg) PBzMA =54°C instead of (Tg) PSt =100°C] [22], leading to the formation of more flexible and easily processable copolymeric structures.…”
Section: Introductionmentioning
confidence: 99%