Multisegmented polymers via step-growth and RAFT miniemulsion polymerization

2021 ◽  
Author(s):  
Thiago R. Guimarães ◽  
Laura Delafresnaye ◽  
Dewen Zhou ◽  
Christopher Barner-Kowollik ◽  
Per B. Zetterlund
Keyword(s):  
Chain Transfer ◽  
Raft Polymerization ◽  
Miniemulsion Polymerization ◽  
Reversible Addition ◽  
Step Growth

We report a method to efficiently prepare multisegmented polymers via a combination of step-growth (SG) and reversible addition-fragmentation chain transfer (RAFT) polymerization.

Reversible Addition–Fragmentation Chain Transfer (RAFT) Polymerization in Miniemulsion Based on In Situ Surfactant Generation

2011 ◽  
Vol 64 (8) ◽  
pp. 1033 ◽  
Author(s):  
S. R. Simon Ting ◽  
Eun Hee Min ◽  
Per B. Zetterlund
Keyword(s):  
Potassium Hydroxide ◽  
Colloidal Stability ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Miniemulsion Polymerization ◽  
High Energy ◽  
Reversible Addition ◽  
Raft Agent ◽  
Surface Active

Reversible addition–fragmentation chain transfer (RAFT) polymerization of styrene has been implemented in aqueous miniemulsion based on the in situ surfactant generation approach using oleic acid and potassium hydroxide in the absence of high energy mixing. The best results were obtained using the RAFT agent 3-benzylsulfanyl thiocarbonyl sufanylpropionic acid (BSPAC), most likely as a result of the presence of a carboxylic acid functionality in the RAFT agent that renders it surface active and thus imparts increased colloidal stability. Stable final miniemulsions were obtained with no coagulum with particle diameters less than 200 nm. The results demonstrate that the RAFT miniemulsion polymerization of styrene employing the low energy in situ surfactant method is challenging, but that a system that proceeds predominantly by a miniemulsion mechanism can be achieved under carefully selected conditions.

A facile route to segmented copolymers by fusing ambient temperature step-growth and RAFT polymerization

2017 ◽  
Vol 53 (77) ◽  
pp. 10648-10651 ◽  
Author(s):  
Thomas Gegenhuber ◽  
Alexander M. Schenzel ◽  
Anja S. Goldmann ◽  
Per B. Zetterlund ◽  
Christopher Barner-Kowollik
Keyword(s):  
Ambient Temperature ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Diels Alder ◽  
Facile Synthesis ◽  
Segmented Copolymers ◽  
Reversible Addition ◽  
Step Growth ◽  
Step Growth Polymerization ◽  
Facile Route

We introduce the facile synthesis of segmented copolymers via a catalyst-free Diels–Alder (DA) reaction at ambient temperature via step-growth polymerization and subsequent reversible addition fragmentation chain transfer (RAFT) polymerization.

Self-Healing Hydrophobic POSS-functionalized Fluorinated Copolymer via RAFT Polymerization and dynamic Diels-Alder Reaction

2021 ◽  
Author(s):  
Siva Ponnupandian ◽  
Prantik Mondal ◽  
Thomas Becker ◽  
Richard Hoogenboom ◽  
Andrew B Lowe ◽  
...  
Keyword(s):  
Chain Transfer ◽  
Raft Polymerization ◽  
Alder Reaction ◽  
Diels Alder ◽  
Self Healing ◽  
Diels Alder Reaction ◽  
Reversible Addition

This investigation reports the preparation of a tailor-made copolymer of furfuryl methacrylate (FMA) and trifluoroethyl methacrylate (TFEMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization. The furfuryl groups of the copolymer...

scholarly journals Nano-Assemblies from Amphiphilic PnBA-b-POEGA Copolymers as Drug Nanocarriers

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1164
Author(s):  
Angeliki Chroni ◽  
Thomas Mavromoustakos ◽  
Stergios Pispas
Keyword(s):  
Molecular Weight ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Polymeric Nanocarriers ◽  
Reversible Addition ◽  
2D Noesy ◽  
Drug Nanocarriers ◽  
Glycol Methyl Ether ◽  
Different Molecular Weight

The focus of this study is the development of highly stable losartan potassium (LSR) polymeric nanocarriers. Two novel amphiphilic poly(n-butyl acrylate)-block-poly(oligo(ethylene glycol) methyl ether acrylate) (PnBA-b-POEGA) copolymers with different molecular weight (Mw) of PnBA are synthesized via reversible addition fragmentation chain transfer (RAFT) polymerization, followed by the encapsulation of LSR into both PnBA-b-POEGA micelles. Based on dynamic light scattering (DLS), the PnBA30-b-POEGA70 and PnBA27-b-POEGA73 (where the subscripts denote wt.% composition of the components) copolymers formed micelles of 10 nm and 24 nm in water. The LSR-loaded PnBA-b-POEGA nanocarriers presented increased size and greater mass nanostructures compared to empty micelles, implying the successful loading of LSR into the inner hydrophobic domains. A thorough NMR (nuclear magnetic resonance) characterization of the LSR-loaded PnBA-b-POEGA nanocarriers was conducted. Strong intermolecular interactions between the biphenyl ring and the butyl chain of LSR with the methylene signals of PnBA were evidenced by 2D-NOESY experiments. The highest hydrophobicity of the PnBA27-b-POEGA73 micelles contributed to an efficient encapsulation of LSR into the micelles exhibiting a greater value of %EE compared to PnBA30-b-POEGA70 + 50% LSR nanocarriers. Ultrasound release profiles of LSR signified that a great amount of the encapsulated LSR is strongly attached to both PnBA30-b-POEGA70 and PnBA27-b-POEGA73 micelles.

Synthesis and characterization of a naphthalimide–dye end-labeled copolymer by reversible addition–fragmentation chain transfer (RAFT) polymerization

2011 ◽  
Vol 89 (3) ◽  
pp. 317-325 ◽  
Author(s):  
Binxin Li ◽  
Daniel Majonis ◽  
Peng Liu ◽  
Mitchell A. Winnik
Keyword(s):  
Chain Transfer ◽  
Raft Polymerization ◽  
Polymer Composition ◽  
Cooh Group ◽  
Agent Based ◽  
Molecular Weights ◽  
Reversible Addition ◽  
Raft Agent ◽  
End Use ◽  
Naphthalimide Dye

We describe the synthesis of an end-functionalized copolymer of N-(2-hydroxypropyl)methacrylamide (HPMA) and N-hydroxysuccinimide methacrylate (NMS) by reversible addition–fragmentation chain transfer (RAFT) polymerization. To control the polymer composition, the faster reacting monomer (NMS) was added slowly to the reaction mixture beginning 30 min after initating the polymerization (ca. 16% HPMA conversion). One RAFT agent, based on azocyanopentanoic acid, introduced a –COOH group to the chain at one end. Use of a different RAFT agent containing a 4-amino-1,8-naphthalimide dye introduced a UV–vis absorbing and fluorescent group at this chain end. The polymers obtained had molecular weights of 30 000 and 20 000, respectively, and contained about 30 mol% NMS active ester groups.

Living Radical Polymerization with Reversible Addition−Fragmentation Chain Transfer (RAFT Polymerization) Using Dithiocarbamates as Chain Transfer Agents

1999 ◽  
Vol 32 (21) ◽  
pp. 6977-6980 ◽  
Author(s):  
Roshan T. A. Mayadunne ◽  
Ezio Rizzardo ◽  
John Chiefari ◽  
Yen Kwong Chong ◽  
Graeme Moad ◽  
...  
Keyword(s):  
Radical Polymerization ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Living Radical Polymerization ◽  
Reversible Addition ◽  
Transfer Agents

Controlling Mechanical Properties of 3D Printed Polymer Composites through Photoinduced Reversible Addition-Fragmentation Chain Transfer (RAFT) Polymerization

2021 ◽  
Author(s):  
Xiaobing Shi ◽  
Jin Zhang ◽  
Nathaniel Alan Corrigan ◽  
Cyrille Boyer
Keyword(s):  
Mechanical Properties ◽  
Silica Nanoparticles ◽  
Polymer Composites ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Polymer Networks ◽  
Material Design ◽  
Advanced Material ◽  
Reversible Addition ◽  
3D Printed

Reversible addition-fragmentation chain-transfer (RAFT) polymerization has been widely exploited to produce homogeneous and living polymer networks for advanced material design. In this work, we incorporate silica nanoparticles (SNPs) into a...

Preparation of azobenzene-terminated polymers via reversible addition-fragmentation chain transfer (RAFT) polymerization

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Xiaoming Wan ◽  
Zhengbiao Zhang ◽  
Xiulin Zhu ◽  
Jian Zhu ◽  
Zhenping Cheng
Keyword(s):  
Methyl Methacrylate ◽  
Fluorescence Spectra ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
Reversible Addition ◽  
Azobenzene Moiety

AbstractThree azobenzene-based dithiocarbamates, 2-(phenylazo-phenoxycarbonyl) prop-2-yl 9H-carbazole-9-carbodithioate (APCDT), 2-(4-nitro-phenylazophenoxy- carbonyl)prop-2-yl 9H-carbazole-9-carbodithioate (ANPCDT), 2-(4-cyanophenylazo- phenoxy-carbonyl)pro-2-yl 9H-carbazole-9-carbodithioate (ACPCDT), were synthesized and used as RAFT agents in the polymerizations of styrene (St) and methyl methacrylate (MMA). The results showed that APCDT, ACPCDT and ANPCDT were effective RAFT agents for the polymerization of St. In the case of MMA, the polymerization showed hybrid behavior. The different substitutes on azobenzene moiety in dithiocarbamates did not show obvious influence on the controllability of the polymerizations. The UV and fluorescence spectra of RAFT agents and obtained azobenzene-terminated polymers were investigated

scholarly journals Reversible addition fragmentation chain transfer polymerization - RAFT

2004 ◽  
Vol 58 (11) ◽  
pp. 514-520
Author(s):  
Milena Avramovic ◽  
Lynne Katsikas ◽  
Branko Dunjic ◽  
Ivanka Popovic
Keyword(s):  
Radical Polymerization ◽  
Chain Transfer ◽  
Raft Polymerization ◽  
General Structure ◽  
Controlled Radical Polymerization ◽  
Molecular Structures ◽  
Reversible Addition ◽  
Chain Transfer Polymerization

The fundamentals of controlled radical polymerization are presented in this review. The paper focuses on reversible addition fragmentation chain transfer (RAFT) polymerization. The mechanism and specifics of this type of polymerization are discussed, as are the possibilities of synthesizing complex macro-molecular structures. The synthesis and properties of RAFT agents, of the general structure Z-C(=S)-S-R, are presented.

Sign in / Sign up

Export Citation Format

Share Document