RAFT-Polymerization-Induced Self-Assembly and Reorganizations: Ultrahigh-Molecular-Weight Polymer and Morphology-Tunable Micro-/Nanoparticles in One Pot

2016 ◽  
Vol 37 (21) ◽  
pp. 1735-1741 ◽  
Author(s):  
Xiao-Yun Zhang ◽  
Dong-Ming Liu ◽  
Xin-Hu Lv ◽  
Miao Sun ◽  
Xiao-Li Sun ◽  
...  
2018 ◽  
Vol 9 (13) ◽  
pp. 1593-1602 ◽  
Author(s):  
Fabian H. Sobotta ◽  
Franziska Hausig ◽  
Dominic O. Harz ◽  
Stephanie Hoeppener ◽  
Ulrich S. Schubert ◽  
...  

Combining a sequential, one-pot RAFT polymerization with the polymerization-induced self-assembly process results in a versatile oxidation-responsive carrier system.


Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 827
Author(s):  
Xiaowei An ◽  
Weihong Lu ◽  
Jian Zhu ◽  
Xiangqiang Pan ◽  
Xiulin Zhu

Selenide-containing amphiphilic copolymers have shown significant potential for application in drug release systems. Herein, we present a methodology for the design of a reactive oxygen species-responsive amphiphilic diblock selenide-labeled copolymer. This copolymer with controlled molecular weight and narrow molecular weight distribution was prepared by sequential organoselenium-mediated reversible addition fragmentation chain transfer (Se-RAFT) polymerization and selenol-based nucleophilic reaction. Nuclear magnetic resonance (NMR) and matrix-assisted laser desorption/ionization time-to-flight (MALDI-TOF) techniques were used to characterize its structure. Its corresponding nanomicelles successfully formed through self-assembly from the copolymer itself. Such nanomicelles could rapidly disassemble under oxidative conditions due to the fragmentation of the Se–C bond. Therefore, this type of nanomicelle based on selenide-labeled amphiphilic copolymers potentially provides a new platform for drug delivery.


2012 ◽  
Vol 50 (19) ◽  
pp. 4103-4109 ◽  
Author(s):  
Hongjuan Jiang ◽  
Lifen Zhang ◽  
Jian Qin ◽  
Wei Zhang ◽  
Zhenping Cheng ◽  
...  

Nanomaterials ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1779
Author(s):  
Federica Zuppardi ◽  
Mario Malinconico ◽  
Franck D’Agosto ◽  
Giovanna Gomez D’Ayala ◽  
Pierfrancesco Cerruti

Thermo-responsive copolymers based on oligo(ethylene glycol) methacrylate (OEGMA, Mn = 300 g/mol) and pentafluorostyrene (PFS), coded PFG, were synthesized by RAFT polymerization, using a trithiocarbonate (CTTPC) as controlling agent. Different molar masses were targeted and dispersities lower than 1.51 were obtained. The thermally triggered self-assembly of the resulting PFG copolymers in water was investigated by dynamic light scattering (DLS). The lower critical solution temperature (LCST) slightly increased with the molecular weight in the 26–30 °C temperature range, whereas the sizes of the intermicellar aggregates formed upon self-assembly tended to decrease with increasing molecular weights (ranging from 1415 to 572 nm). The resulting thermally-induced polymer aggregates were then used to encapsulate and remove organic contaminants from water. Nile Red (NR) and Thiazole yellow G (TYG) were employed as hydrophobic and hydrophilic model contaminants, respectively. Experimental results evidenced that higher molecular weight copolymers removed up to 90% of NR from aqueous solution, corresponding to about 10 mg of dye per g of copolymer, regardless of NR concentration. The removal of TYG was lower with respect to NR, decreasing from about 40% to around 20% with TYG concentration. Finally, the copolymers were shown to be potentially recycled and reused in the treatment of contaminated water.


Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1107 ◽  
Author(s):  
Ahmad Joumaa ◽  
Florence Gayet ◽  
Eduardo J. Garcia-Suarez ◽  
Jonas Himmelstrup ◽  
Anders Riisager ◽  
...  

A latex of amphiphilic star polymer particles, functionalized in the hydrophobic core with nixantphos and containing P(MAA-co-PEOMA) linear chains in the hydrophilic shell (nixantphos-functionalized core-crosslinked micelles, or nixantphos@CCM), has been prepared in a one-pot three-step convergent synthesis using reversible addition-fragmentation chain transfer (RAFT) polymerization in water. The synthesis involves polymerization-induced self-assembly (PISA) in the second step and chain crosslinking with di(ethylene glycol) dimethacrylate (DEGDMA) in the final step. The core consists of a functionalized polystyrene, obtained by incorporation of a new nixantphos-functionalized styrene monomer (nixantphos-styrene), which is limited to 1 mol%. The nixantphos-styrene monomer was synthesized in one step by nucleophilic substitution of the chloride of 4-chloromethylstyrene by deprotonated nixantphos in DMF at 60 °C, without interference of either phosphine attack or self-induced styrene polymerization. The polymer particles, after loading with the [Rh(acac)(CO)2] precatalyst to yield Rh-nixantphos@CCM, function as catalytic nanoreactors under aqueous biphasic conditions for the hydroformylation of 1-octene to yield n-nonanal selectively, with no significant amounts of the branched product 2-methyl-octanal.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Wei Cao ◽  
Senlin Xia ◽  
Michael Appold ◽  
Nitin Saxena ◽  
Lorenz Bießmann ◽  
...  

AbstractUltrahigh molecular weight (UHMW) diblock copolymers (DBCs) have emerged as a promising template for fabricating large-sized nanostructures. Therefore, it is of high significance to systematically study the influence of film thickness and solvent vapor annealing (SVA) on the structure evolution of UHMW DBC thin films. In this work, spin coating of an asymmetric linear UHMW polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) DBC is used to fabricate thin films, which are spherically structured with an inter-domain distance larger than 150 nm. To enhance the polymer chain mobility and facilitate approaching equilibrium nanostructures, SVA is utilized as a post-treatment of the spin coated films. With increasing film thickness, a local hexagonal packing of PMMA half-spheres on the surface can be obtained, and the order is improved at larger thickness, as determined by grazing incidence small angle X-ray scattering (GISAXS). Additionally, the films with locally hexagonal packed half-spherical morphology show a poor order-order-poor order transition upon SVA, indicating the realization of ordered structure using suitable SVA parameters.


RSC Advances ◽  
2015 ◽  
Vol 5 (28) ◽  
pp. 21580-21587 ◽  
Author(s):  
Zhenghe Zhang ◽  
Lizhi Hong ◽  
Jinxia Li ◽  
Feng Liu ◽  
Haibo Cai ◽  
...  

The amphiphilic alternating copolymer brushes P(MIPOSS-alt-VBPEG) with a sequence of alternating MIPOSS and polyethylene glycol (PEG) side chains were synthesized via RAFT polymerization, and they could form spherical aggregates.


2017 ◽  
Vol 8 (46) ◽  
pp. 7217-7228 ◽  
Author(s):  
Povilas Radzevicius ◽  
Medeina Steponaviciute ◽  
Tatjana Krivorotova ◽  
Ricardas Makuska

Pentablock copolymers synthesized by one-pot successive RAFT polymerization are double thermoresponsive and exhibit block sequence dependent aggregation in aqueous solutions.


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