Synthesis, Functionalization and Reductive Degradation of Multibrominated Disulfide-containing Hyperbranched Polymers

2012 ◽  
Vol 65 (1) ◽  
pp. 28 ◽  
Author(s):  
Delia-Laura Popescu ◽  
Nicolay V. Tsarevsky

Reductively degradable hyperbranched polymethacrylates with multiple peripheral alkyl bromide groups were synthesized by the azobis(2-isobutyronitrile)-initiated copolymerization of diethylene glycol methyl ether methacrylate or oligo(ethylene oxide) methyl ether methacrylate with the disulfide-containing crosslinker bis(2-methacryloyloxyethyl)disulfide (2.5–10.0 mol-% relative to the monomer) in the presence of carbon tetrabromide (10–40-fold excess relative to the radical initiator) as efficient chain transfer agent. The alkyl bromide groups initiated the atom-transfer radical polymerization of methyl methacrylate, and star copolymers with hyperbranched disulfide-containing cores were formed. Both the macroinitiators and the star copolymers derived from them were degraded in reducing environment.

RSC Advances ◽  
2017 ◽  
Vol 7 (37) ◽  
pp. 23114-23121 ◽  
Author(s):  
Jianbo Tan ◽  
Dongdong Liu ◽  
Xuechao Zhang ◽  
Chundong Huang ◽  
Jun He ◽  
...  

We report a photoinitiated dispersion polymerization of 2-hydroxypropyl methacrylate (HPMA) in the presence of silica nanoparticles using a poly(ethylene glycol) methyl ether (mPEG) macromolecular chain transfer agent (macro-CTA).


2019 ◽  
Vol 13 (3) ◽  
pp. 35 ◽  
Author(s):  
Jehad A. A. Yamin ◽  
Mohammad Samih Hijazi ◽  
Mohammad A. Hamdan

Toyota car fitted with smoke meter to measure the opacity in the exhaust was used. Five different types of oxygenates were used with the concentration of each one varied between 5 to 20% by volume at an increment of 5%. The results show a significant reduction in the opacity of the exhaust products. A maximum of 70% reduction was achieved when 15% ethanol was added at 3000 RPM, and 62% reduction when 20% methanol was added at same speed. As for Dimethoxy Ethane (DMET), a maximum reduction of 30% was achieved at 3000 RPM and that of Tri-propylene glycol methyl ether (TPGME) was 27.3% at same speed. Diethylene glycol monoethyl ether (DGME) did not show encouraging results as a maximum reduction of 10.3% was achieved at 2000 RPM with 5% of DGME. Further, it was found that the reduction in the opacity level was less significant when the filter was used. This, perhaps, is due to the nature of the DPF used.


2015 ◽  
Vol 16 (10) ◽  
pp. 3275-3285 ◽  
Author(s):  
Barbara Mendrek ◽  
Łukasz Sieroń ◽  
Iwona Żymełka-Miara ◽  
Paulina Binkiewicz ◽  
Marcin Libera ◽  
...  

2015 ◽  
Vol 6 (9) ◽  
pp. 1639-1648 ◽  
Author(s):  
D. Meza ◽  
E. Arias ◽  
I. Moggio ◽  
J. Romero ◽  
J. M. Mata ◽  
...  

The strong π–π interaction that governs (diethylene glycol methyl ether) benzoateethynylene macromolecules was evidenced by X-ray scattering and HRTEM.


2009 ◽  
Vol 62 (11) ◽  
pp. 1496 ◽  
Author(s):  
Steevens N. S. Alconcel ◽  
Gregory N. Grover ◽  
Nicholas M. Matsumoto ◽  
Heather D. Maynard

Ionomers containing sodium 4-styrene sulfonate (4SS) and poly(ethylene glycol) methyl ether acrylate (PEGA) were synthesized by reversible addition–fragmentation chain transfer (RAFT) polymerization. The polymerization was mediated by 1-phenylethyl dithiobenzoate chain transfer agent in a dimethylformamide/water solvent system. Well-defined copolymers of pPEGA-co-4SS were produced with molecular weights ranging from 10 to 40 kDa and polydispersity indices of 1.06–1.18 by gel permeation chromatography against monodisperse poly(methyl methacrylate) standards. After polymerization, the dithioester was reduced and trapped in situ with divinyl sulfone to produce a well-defined, semitelechelic pPEGA-co-4SS Michael acceptor polymer. UV-visible, infrared, and 1H NMR spectroscopy confirmed that the integrity of the polymer backbone was maintained and that the vinyl sulfone was successfully incorporated at the chain end.


Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1657 ◽  
Author(s):  
Ramírez-Jiménez ◽  
Montoya-Villegas ◽  
Licea-Claverie ◽  
Gónzalez-Ayón

Thermo-responsive polymers and copolymers derivatives of oligo(ethylene glycol) methyl ether methacrylate (Mn = 300 g mol−1) (OEGMA) and di(ethylene glycol) methyl ether methacrylate (DEGMA) have been synthesized by reversible addition fragmentation chain transfer polymerization (RAFT) using 5-amino-4-methyl-4-(propylthiocarbonothioylthio)-5-oxopentanoic acid (APP) as chain transfer agent (CTA). The monomer conversion was evaluated by hydrogen nuclear magnetic resonance (1H-NMR); number average molecular weights (Mn), weight average molecular weight (Mw), and dispersity (Đ) were obtained by gel permeation chromatography (GPC); glass transition temperature (Tg) was evaluated by modulated differential scanning calorimetry (DSC), cloud point temperature (Tcp) was measured and compared by turbidimetry and dynamic light scattering (DLS). The effect of polymer composition and concentration on the Tcp, either in water or in phosphate buffer saline (PBS), was studied. The values of Tcp using PBS were between 3 and 4 °C lower than using water. Results showed an ideal copolymerization behavior; therefore, the Tcp could be tuned by an adequate monomers feed ratio obtaining polymers which may be used in drug delivery and other applications.


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