Synthesis of poly(N-(2-hydroxypropyl) methacrylamide) brushes by interface-mediated RAFT polymerization

RSC Advances ◽  
2016 ◽  
Vol 6 (51) ◽  
pp. 45259-45264 ◽  
Author(s):  
Ertan Yildirim ◽  
Dilek Cimen ◽  
Adem Zengin ◽  
Tuncer Caykara

A novel poly(N-(2-hydroxypropyl) methacrylamide) [poly(HPMA)] brush with a moderate density polymer brush (0.52 chains per nm2) was synthesized by an interface-mediated RAFT polymerization.

2021 ◽  
Vol 162 ◽  
pp. 104875
Author(s):  
Vladimir Sincari ◽  
Svetlana Lukáš Petrova ◽  
Rafał Konefał ◽  
Martin Hruby ◽  
Eliézer Jäger

Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 706 ◽  
Author(s):  
Chaoqun Wu ◽  
Yudan Zhou ◽  
Haitao Wang ◽  
Jianhua Hu

Zwitterionic polymers are suitable for replacing poly(ethylene glycol) (PEG) polymers because of their better antifouling properties, but zwitterionic polymers have poor mechanical properties, strong water absorption, and their homopolymers should not be used directly. To solve these problems, a reversible-addition fragmentation chain transfer (RAFT) polymerization process was used to prepare copolymers comprised of zwitterionic side chains that were attached to an ITO glass substrate using spin-casting. The presence of 4-vinylpyridine (4VP) and zwitterion chains on these polymer-coated ITO surfaces was confirmed using 1H NMR, FTIR, and GPC analyses, with successful surface functionalization confirmed using water contact angle, X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) studies. Changes in water contact angles and C/O ratios (XPS) analysis demonstrated that the functionalization of these polymers with β-propiolactone resulted in hydrophilic mixed 4VP/zwitterionic polymers. Protein adsorption and cell attachment assays were used to optimize the ratio of the zwitterionic component to maximize the antifouling properties of the polymer brush surface. This work demonstrated that the antifouling surface coatings could be readily prepared using a “P4VP-modified” method, that is, the functionality of P4VP to modify the prepared zwitterionic polymer. We believe these materials are likely to be useful for the preparation of biomaterials for biosensing and diagnostic applications.


2017 ◽  
Vol 8 (48) ◽  
pp. 7499-7506 ◽  
Author(s):  
Binbin Xu ◽  
Xiaowen Sun ◽  
Chaoqun Wu ◽  
Jianhua Hu ◽  
Xiaoyu Huang

This article reports the synthesis of a semi-fluorinated compositional heterogeneous polymer brush for anti-fouling surface.


2015 ◽  
Vol 6 (38) ◽  
pp. 6812-6818 ◽  
Author(s):  
Dilek Cimen ◽  
Tuncer Caykara

A novel micro-patterned poly(AHMA) brush was prepared by a combination of photolithography and interface mediated RAFT polymerization for DNA hybridization. By this method, highly resolved micro-patterned polymer brush structures down to ∼2.0 μm lines were obtained.


2014 ◽  
Vol 5 (5) ◽  
pp. 1711-1719 ◽  
Author(s):  
Harald Wutzel ◽  
Felix H. Richter ◽  
Yuanchao Li ◽  
Sergei S. Sheiko ◽  
Harm-Anton Klok

2009 ◽  
Vol 62 (10) ◽  
pp. 1344 ◽  
Author(s):  
David Valade ◽  
Cyrille Boyer ◽  
Thomas P. Davis ◽  
Volga Bulmus

Block copolymers of allyl methacrylate and N-(2-hydroxypropyl)methacrylamide (HPMA) with different block lengths have been synthesized by reversible addition–fragmentation chain transfer polymerization. Allyl groups were modified with cysteamine, via a thiol-ene photoreaction, with a high efficiency (~100%) as evidenced by NMR spectroscopy, yielding cationic copolymers of HPMA. Polyelectrolyte complexes of small interfering RNAs (siRNA) and the cationic block copolymers were then formed at an N/P ratio between 1 and 4 depending on the block length of the copolymers. Increasing the length of the hydrophilic block was found to decrease the efficiency of siRNA complexation. The hydrodynamic diameter of the polyplexes in 130 mM buffer solution was less than 100 nm.


2014 ◽  
Vol 5 (8) ◽  
pp. 2816-2823 ◽  
Author(s):  
S. P. Le-Masurier ◽  
G. Gody ◽  
S. Perrier ◽  
A. M. Granville

One-pot ‘grafting from’ of polystyrene on polydopamine particles was investigated using a newly developed carbonyl-azide reversible addition–fragmentation chain transfer (RAFT) agent.


2021 ◽  
Vol 69 (4) ◽  
Author(s):  
Tobias A. Gmür ◽  
Joydeb Mandal ◽  
Juliette Cayer-Barrioz ◽  
Nicholas D. Spencer

AbstractTo meet the need for oil-compatible friction modifier additives that can significantly reduce energy consumption in the boundary-lubrication regime, a macromolecular design approach has been taken. The aim was to produce a lubricious polymer film on the sliding surfaces. A series of readily functionalizable block copolymers carrying an oleophilic poly(dodecyl methacrylate) block and a functionalizable poly(pentafluorophenyl methacrylate) block of various lengths was synthesized by means of reversible addition-fragmentation chain-transfer (RAFT) polymerization. The poly(pentafluorophenyl methacrylate) block was used to attach surface-active nitrocatechol anchoring groups to the polymer. The friction-reduction properties of these polymers were assessed with 0.5 wt% solutions in hexadecane by means of rolling-sliding macroscopic tribological tests. Block copolymers with roughly equal block lengths and moderate molecular weights were significantly more effective at friction reduction than all other architectures investigated. They also displayed lower friction coefficients than glycerol monooleate—a commercially used additive. The film-formation ability of these polymers was examined using a quartz-crystal microbalance with dissipation (QCM-D), by monitoring their adsorption onto an iron oxide-coated QCM crystal. The polymer with highest lubrication efficiency formed a thin film of ~ 17 nm thickness on the crystal, indicating the formation of a polymer brush. Interferometric rolling-sliding experiments with the same polymer showed a separating film thickness of ~ 20 nm, which is consistent with the QCM-D value, bearing in mind the compression of the adsorbed layers on the two sliding surfaces during tribological testing. Graphical Abstract


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