ライフサイエンスコーパス: copolymer

1 used in the characterization of the obtained copolymer.

2 hierarchical structures from a single block copolymer.

3 ypropyl methacrylate) [PHPMAC-PHPMA] diblock copolymer.

4 owth process from a liquid crystalline block copolymer.

5 nalized 3,4-propylenedioxythiophene (ProDOT) copolymer.

6 block (PMestOx) of the PMeOx-PMestOx diblock copolymer.

7 f compositions starting from a single parent copolymer.

8 e step from an amphiphilic bottlebrush block copolymer.

9 emblies captured by the methylamine-modified copolymer.

10 f cyclic peptide-bridged amphiphilic diblock copolymers.

11 an be expanded to donor-acceptor alternating copolymers.

12 gy by synthesizing and functionalizing block copolymers.

13 -assembly and microphase-separation of block copolymers.

14 emonstrated through the preparation of block copolymers.

15 ew 2D homopolymers and one (of three) new 2D copolymers.

16 to their analogs generated from statistical copolymers.

17 the formation of rod-coil and rod-rod block copolymers.

18 y(ethylene glycol)-block-poly(glutamic acid) copolymers.

19 ssembled structure of achiral-chiral diblock copolymers.

20 olymerization to form polyolefin-polar block copolymers.

21 ers, we produced a range of block and random copolymers.

22 e synthesis of well-defined di- and triblock copolymers.

23 macroinitiator for the synthesis of triblock copolymers.

24 ylene, polyvinyl chloride and vinyl chloride copolymers.

25 of dispersity on the self-assembly of block copolymers.

26 tension produces all-conjugated n-type block copolymers.

27 of chain copolymerization for covalent block copolymers.

28 aste containing 0.3% triclosan + 2.0% PVM/MA copolymer + 1450 ppm fluoride (test) or (2) toothpaste c

29 traditional ionic linkages, the alternating copolymer (AB)(n) shows weaker adhesion strength more si

30 om foods and vegetables using an amphiphilic copolymer adsorbent, poly(styrene)-co-2-vinylpyridine wh

31 ymers, a random (statistical) supramolecular copolymer, an alternate supramolecular copolymer, or a c

32 much higher conductivities than their block copolymer analogs.

33 ylnorbornenes afforded both a soluble linear copolymer and a cross-linked organogel.

34 l sheet surfaces for cell culturing, however copolymer and interpenetrated polymer networks based on

35 ubunits were readily incorporated into block copolymers and could be modified through subsequent tran

36 additional insights into the composition of copolymers and length distributions of the species over

37 ved using complex and expensive synthesis of copolymers and terpolymers or via irradiation with high-

38 ncies depending on both the structure of the copolymers and the membrane proteins.

39 ides rapid access to a wide range of diblock copolymers, and enables fundamental thermodynamic parame

40 s of a poly(p-arylenediethynylene phosphine) copolymer are 35 or 94 times more emissive when treated

41 The bulk properties of a copolymer are directly affected by monomer sequence, yet

42 Supramolecular copolymers are an emerging class of materials, and in th

43 Olefin copolymers are complex polymer materials that exhibit mu

44 tlook towards applications in which tailored copolymers are ideally suited.

45 the self-assembled nanostructures from block copolymers are limited to spherical micelles, wormlike m

46 Charged block copolymers are of great interest due to their unique sel

47 e reactions when vesicles containing diblock copolymers are present.

48 nt of polysorbate 80, glycerin, and carbomer copolymer as well as the area of oil-water interface wer

49 ed poly(ethylene glycol)-poly(glutamic acid) copolymers as excipients suitable to be formulated into

50 uccess has been achieved to date using block copolymers as precursors.

51 nto linear polymers; therefore, we monitored copolymers assembled in vitro after incubation with ClpX

52 We describe here a block copolymer assembly system that combines desirable charac

53 hrough seeded growth of crystallizable block copolymers at the termini of immobilized, surface-confin

54 Biocompatible copolymers based on N-(2-hydroxypropyl)methacrylamide (H

55 nticancer nanomedicine - specifically a HPMA copolymer-based drug delivery system.

56 Core-shell BB block copolymers (BBCPs) are shown to quantitatively depolymer

57 etween 16 and 108 nm using bottlebrush block copolymers (BBCPs) as templates.

58 wever, the synthesis of supramolecular block copolymers (BCPs) constitutes a significant challenge du

59 Directed self-assembly of block copolymers (BCPs) enables nanofabrication at sub-10 nm d

60 The ability to synthesize well-defined block copolymers (BCPs) from one-pot comonomer mixtures has po

61 The directed self-assembly (DSA) of block copolymers (BCPs) has shown promise in fabricating custo

62 in the synthesis of a large variety of block copolymers (BCPs) with structural and functional diversi

63 yclohexylglycolide) (PCG)-based chiral block copolymers (BCPs*), poly(benzyl methacrylate)-b-poly(d-c

64 ation of pancreatic islets seeded within the copolymer bioscaffold supports long-term cell viability,

65 atterns from combinatorial polymer and block copolymer brushes.

66 nt of self-healing efficiency of hydrophobic copolymers by a factor of three.

67 ads to the formation of supramolecular block copolymers by chain-growth process from the seed termini

68 report the formation of supramolecular block copolymers by two-component seeded living polymerization

69 copolymer, or a complex supramolecular block copolymer can occur, determined by their intermolecular

70 nt sequence selectivity for AB- and ABB-type copolymers can be achieved with a single dimagnesium cat

71 butylammonium chloride, we show that diblock copolymers can be readily synthesized via ROMPISA in sol

72 regular PMMA/polyethylene glycol (PEG) block copolymers capable of undergoing crystallization driven

73 s made by using multi-scale conjugated block-copolymer-carbon nanotube-polyurethane foam assemblies a

74 f the minimum number of phosphate groups per copolymer chain required to promote nanoparticle occlusi

75 In addition, the pre-organization of copolymer chains within sterically-stabilized nanopartic

76 ed using solution-cast molecularly-dissolved copolymer chains.

77 rated to be applicable to a variety of block copolymer chemistries on multigram scales with excellent

78 These gradient copolymers combine the high structural modularity of pol

79 The copolymer complexes show no complement activation, and i

80 logy and SAXS studies indicate that a single copolymer composition can form well-defined spheres (4 d

81 facilitate self-healing in relatively narrow copolymer compositional range.

82 Previous studies have shown that copolymer compositions can significantly impact self-hea

83 This approach utilizes smart copolymers comprised of poly(ethylene glycol) (PEG) and

84 A series of copolymers comprising a terpyridine ligand and various f

85 morphologies to be reproducibly targeted at copolymer concentrations ranging from 10 to 30% w/w soli

86 trolyte is attributed to the use of a unique copolymer consisting of a soft ether domain and a hard c

87 is, and characterization of an unprecedented copolymer consisting of alternating linear and dendritic

88 The amphiphilic block copolymer, consisting of a hydrophobic poly(methyl metha

89 Here, we report the facile synthesis of a copolymer containing quinine and 2-hydroxyethyl acrylate

90 A series of random copolymers containing dipicolylamine as binding motifs a

91 Amphiphilic block copolymers covalently functionalized with sulfonic acid

92 A cross-linked random copolymer demonstrated a high level of hydroxide conduct

93 Block copolymer design features were specifically tailored to

94 and observed that ClpXP promotes rapid MinCD copolymer destabilization and direct MinD degradation by

95 boundary mode conditions whereas the random copolymer did not.

96 d-like and open-like conformations using the copolymer diisobutylene/maleic acid (DIBMA) for structur

97 gent mesostructure-based properties in block-copolymer-directed metal, semiconductor, and superconduc

98 The copolymer displays bacteria-activated surfactant-like pr

99 The copolymer-DOX was further loaded with nifuroxazide (NFX)

100 ilarity/difference between random amino acid copolymer drugs using liquid chromatography mass spectro

101 methyl signal from SCB in an ethylene-hexene copolymer (EH, 3.6 mol % H) in 3.5 min with 0.5 mug of s

102 ll membranes using styrene maleic acid (SMA) copolymer, elucidating structures of ASIC1 channels in b

103 siveness of POEGMA-b-P(MAA-co-VSPpaMA) block copolymer enabled the realization of self-amplified phot

104 Both effects emerge only when the copolymers enter cells as polymersomes and their magnitu

105 Vitrimers derived from self-assembling block copolymers exhibit superior resistance to macroscopic de

106 Surprisingly, AAEMs made from the random copolymer exhibited much higher conductivities than thei

107 m periodicity such as self-assembly of block copolymer films can be chemically characterized by IR-Pi

108 The most consistent copolymer films were produced using chronopotentiometry

109 concentration of a thermosensitive triblock copolymer for extended ocular drug delivery.

110 ngs, highlighting the great promise of block copolymers for designing PCF supports for electrochemica

111 sizing both a homopolymer and an alternating copolymer from the same glycol-substituted cyanostar mac

112 mistry to synthesize a series of bottlebrush copolymers from red, green, and blue luminescent macromo

113 The density of the ligands in the block copolymer further regulates the mechanical properties.

114 copic gel-to-sol phase transformation of the copolymer gel, although 99.4% of the organogel is inert

115 s interact with acidic pectins to form block-copolymer gels that can play distinct roles in legume ro

116 on electron microscopy showed that the block copolymers had a disordered microphase segregation which

117 Once nanoparticles formed by the block copolymer have accumulated in a tumor and have been take

118 Since the PHB-Xa block copolymers have a high pai conjugate structure and hydro

119 As representative examples, blends of olefin copolymers have been fractionated on porous graphitic ca

120 for fabricating and controlling ABA triblock copolymer hierarchical structures using solvent-non-solv

121 nding of the phase behavior of charged block copolymers, however, is still at a primitive stage.

122 monstrate for the first time that an abiotic copolymer hydrogel nanoparticle (NP1) engineered to bind

123 ed to synthesize a functionalized norbornene copolymer in a range of molecular weights for specific m

124 ead to the formation of amphiphilic gradient copolymers in a single step.

125 lines to classify and analyze supramolecular copolymers in order to create a fruitful platform to des

126 l-known that the self-assembly of AB diblock copolymers in solution can produce various morphologies

127 periments of poly(d-glucose carbonate) block copolymers in solution that exhibit assembly into spheri

128 alternating/random hydrophobic acrylic-based copolymers in the presence of confined water molecules.

129 The polymer donors are D-A1-D-A2-type random copolymers in which the D and A1 units are monomers orig

130 The mechanism through which these copolymers induce Tregs is unknown.

131 The self-assembly of block copolymers into 1D, 2D and 3D nano- and microstructures

132 ly-L-lactide-block-polyethylene glycol block copolymers into 1D, 2D and 3D nanostructures.

133 This diblock copolymer is an example of a synthetic polymer with lubr

134 Directed self-assembly of block copolymers is a key enabler for nanofabrication of devic

135 nd sequence elucidation of complex homo- and copolymers is key for further understanding polymers, po

136 in thick films (>100 um) derived from block copolymers is reported.

137 rs formed of polydiacetylene (PDA), triblock copolymer (L64 or F68), and sodium dodecyl sulfate (SDS)

138 tegy to enable the rapid generation of block copolymer libraries (100 distinct polymers in 9 min) fro

139 s reported for the rapid generation of block copolymer libraries spanning a wide range of composition

140 Finally, scanning probe block copolymer lithography was used in combination with this

141 catalysts, prepared by scanning probe block copolymer lithography, and chemical vapor deposition.

142 We synthesized amphiphilic block copolymers made of poly(ethylene glycol)-poly(propylene

143 at the method is broadly applicable to block copolymer materials assembled by solvent evaporation.

144 Ultrasonication of a 120 kDa BCOE copolymer mechanically remodels the polymer backbone, an

145 A15 sphere phase in single-component diblock copolymer melts comprising poly(dodecyl acrylate)-block-

146 mean-field theory results for chiral diblock copolymer melts, that the enhanced thermodynamic stabili

147 First, stretchable copolymer membranes that feature outstanding unstrained

148 iling point solvent into the core of a block copolymer micelle, greatly reducing molecular aggregatio

149 lene oxide)-b-polystyrene (PEO-b-PS) diblock copolymer micelles are cross-linked via Friedel-Crafts r

150 o examine the stability of amphiphilic block copolymer micelles in biologic fluids to identify the pr

151 u, of pH-sensitive positron-emitting neutral copolymer micelles into polycationic polymers, which are

152 he hydrophobic core of PLA-PEG-PLA thermogel-copolymer micelles.

153 ich have a crucial impact on determining the copolymer microstructure.

154 olymerizations with activities up to 3400 Kg copolymer mol(-1) -Zr h(-1) atm(-1) , and with comonomer

155 c properties of APP-103, a polyoxalate-based copolymer molecule containing vanillyl alcohol (VA) that

156 and the subsequent evolution in the diblock copolymer morphology from spheres to worms to vesicles a

157 ed methoxy poly(ethylene glycol)-polylactide copolymer (mPEG-PDLLA) and Pluronic (F127).

158 fferent hairpin probes in an alternating DNA copolymer, multiplex recognition of different miRNAs was

159 benzothiadiazole-thiophene alternating donor copolymer named poly{[2,7-(5,5-didecyl-5H-1,8-dithia-as-

160 efficient synthesis of a wide range of block copolymer nano-objects (e.g., spheres, worms or vesicles

161 efficient synthesis of a wide range of block copolymer nano-objects.

162 Synthetic copolymer nanoparticles (NPs), engineered with affinity

163 f two pairs of sterically stabilized diblock copolymer nanoparticles with identical compositions but

164 s the scalable synthesis of functional block copolymer nanoparticles with various morphologies.

165 of well-defined sterically stabilized block copolymer nanoparticles.

166 Diblock copolymer nanoplatforms of methoxy poly(ethylene glycol)

167 de) (PNIPAM), in situ using a starlike block copolymer nanoreactor as model system to resolve the par

168 erein, a general amphiphilic star-like block copolymer nanoreactor strategy for in situ crafting a se

169 fluidic device by electropolymerisation of a copolymer of polypyrrole to which is immobilised a histi

170 ion of dimers and trimers and an alternating copolymer of two different origami structures, and stepw

171 orenewable and degradable plastics, based on copolymers of gamma-butyrolactone and its ring-fused der

172 (PEG-b-PPS) via the self-assembly of diblock copolymers of poly (ethylene glycol) (PEG) and poly (pro

173 avior was observed when amphiphilic triblock copolymers of PS-block-poly(2-vinylpyridine)-block-poly(

174 rk, polyanhydride nanoparticles comprised of copolymers of sebacic acid, 1,6-bis(p-carboxyphenoxy)hex

175 ding various reviews that extensively report copolymers of TFE (listed below).

176 In contrast, styrene maleic acid (SMA) copolymers offer a detergent-free method for biological

177 of thermally-induced adsorption of Pluronic copolymers onto the droplet interface and an increased m

178 sition was evaluated either as an AB diblock copolymer or as a random copolymer, the diblock effectiv

179 g-acting TAF depots can be designed as block copolymers or as homopolymers.

180 cular copolymer, an alternate supramolecular copolymer, or a complex supramolecular block copolymer c

181 ulation-mode OECTs made from the hydrophilic copolymer P-90, where the deliberate functionalization o

182 An amphiphilic copolymer PAVE containing photo-cross-linkable coumarin

183 ated polymeric building blocks, the triblock copolymer PDHF-b-P3EHT-b-PEG and the diblock copolymer P

184 copolymer PDHF-b-P3EHT-b-PEG and the diblock copolymer PDHF-b-PEG, by using fiber-like seeds derived

185 high productivity (multiple chains of block copolymer per metal center).

186 greatly simplifies the exploration of block copolymer phase space across a range of compositions, mo

187 utyrate)-b-poly(vinyl benzyl xanthate) block copolymer (PHB-Xa) for vortex-assisted solid-phase micro

188 e use NEs featured with amphiphilic triblock copolymer (Pluronic F-127) as a model system to extract/

189 monstrate the use of an amphiphilic triblock copolymer, Pluronic F127, to fabricate a self-healing ph

190 the presence of synthetic amphiphilic block copolymers, Pluronics (SP1017).

191 ally, we have synthesized a series of random copolymer (PNDI-CBS(x)) with different molar fractions (

192 rein, we report a (1) O(2) -responsive block copolymer (POEGMA-b-P(MAA-co-VSPpaMA) to enhance PDT via

193 g-polyoleic acid-g-polyethylene glycol graft copolymer (PoleS-PEG) was used as adsorbent in the solid

194 The film of the copolymer poly(3-amino-benzylamine-co-aniline) (PABA) do

195 The D homopolymer and its diblock copolymer poly(ethylene glycol)-block-poly(2-(dimethylam

196 from compositionally symmetric charged block copolymers, poly[(oligo(ethylene glycol) methyl ether me

197 ect of the tannic acid grafted polypropylene copolymers (PP-Tann) retarded oligomerization of the lin

198 hic characterization of single-crystal block copolymer-preceramic nanocomposite films, the structures

199 are well-defined donor-acceptor alternating copolymers prepared using ring-opening metathesis polyme

200 Bottlebrush copolymers provide a covalent route to multicompartment

201 Compositionally asymmetric diblock copolymers provide an attractive platform for understand

202 Nonnatural amphiphiles, such as diblock copolymers, provide an interface that can be synthetical

203 The resulting copolymers readily degrade under hydrolytic conditions,

204 ble, and controllable syntheses of sequenced copolymers remain a defining challenge in polymer scienc

205 r work showcases the ability of this quinine copolymer reporter to not only facilitate effective gene

206 ar treatment concentrations; untargeted HPMA copolymers required 1000-fold higher treatment concentra

207 (L-lysine)-block-poly(ethylene glycol) block copolymer (s-MNPs).

208 g saturated chain ends in an ethylene-octene copolymer sample with a hard 180 degrees (13)C RINEPT pu

209 generate a new functionalizable alternating copolymer scaffold with controlled molecular weight and

210 The PMeOx-PcBOx copolymer self-assemble into polymeric micelles in aqueo

211 y-sized single-crystal nanodiamonds by block copolymer self-assembled nanomask patterning together wi

212 nated and deuterated polymers, and (3) block copolymer self-assemblies.

213 Although much of the focus in ABA triblock copolymer self-assembly has been on equilibrium nanostru

214 mong all the process steps involved in block copolymer self-assembly, solvent annealing plays a domin

215 Cyclic block copolymers self-assemble into compact nanostructures, as

216 thin the same film microstructure of a model copolymer semiconductor.

217 The Cu-copolymers show a 6-8-fold activity enhancement, compare

218 with an incorporated ET unit in the ternary copolymers show up-shifted LUMO energy levels, increased

219 ergent-free method using styrene-maleic acid copolymers (SMA-PSI) have been investigated by pump-to-p

220 These copolymers solubilize, stabilize, and support membrane p

221 Polymer hexosomes are block copolymer solution morphologies that adopt an internal s

222 supramolecular spheres of dendrimers, block copolymers, surfactants and other self-assembling molecu

223 nerated from other soft matter such as block copolymers, surfactants, and other molecules are chiral.

224 odic arrays were subsequently found in block copolymers, surfactants, lipids, glycolipids, and other

225 f these discoveries, robust di- and triblock copolymer syntheses have been demonstrated with olefins

226 y constructed via multiple, individual block copolymer syntheses.

227 acrylic monomers, thereby facilitating block copolymer synthesis from a single Pd(II) complex.

228 we describe the utility of functional block copolymers synthesized by ring-opening metathesis polyme

229 This diblock copolymer, synthesized by sequential reversible addition

230 his temperature and pH-responsive pentablock copolymer system was able to restore miR-345, making xen

231 scopic bulk single crystals with other block copolymer systems, suggesting that the method is broadly

232 rials, prostaglandin biomaterials, and block copolymer systems.

233 ell-defined single-GNR transistors via block copolymer templates.

234 hylene]amino]-1,3-propanediol) forms a block copolymer that binds several biologically relevant metal

235 n allows helicoidal growth of supramolecular copolymers that are comprised of an alternating array of

236 of novel tannin-functionalized polypropylene copolymers that are designed to inhibit the oxidation of

237 -molecular-weight, crystalline isotactic PHA copolymers that are hard, ductile, and tough plastics, a

238 Amphiphilic block copolymers that carry nucleobases in their hydrophobic b

239 ganic semiconductors based on donor-acceptor copolymers that prevents the formation of H(2) O(2) duri

240 zation of pendant photoswitchable conjugated copolymers that reflect the activity found in the relate

241 ess affords well-defined amphiphilic diblock copolymers that simultaneously form original needle-like

242 o produce so-called "high chi-low N" diblock copolymers that undergo nanoscale phase separation in th

243 this is achieved using an amphiphilic block copolymer, that by itself does not form micelles due to

244 into PLA-PEG-PLA, a biodegradable thermogel copolymer, that instantaneously forms a subcutaneous gel

245 er as an AB diblock copolymer or as a random copolymer, the diblock effectively lubricated cartilage

246 the drug payloads to a beta-cyclodextrin-PEG copolymer to form self-assembled nanoparticles.

247 The capability of this new copolymer to solubilize a uniquely diverse set of active

248 gh molecular weight star and dendritic block copolymers to be prepared in a single step under ambient

249 ylic acid-functionalized polycarbonate block copolymers to commercially available bone cement.

250 A cyclic olefin copolymer (TOPAS) suspended-core fiber guiding in the TH

251 rea (PCU) were effective but maleic-itaconic copolymer treated urea was ineffective in reducing ammon

252 Upon heating, the helicoidal copolymers undergo a catastrophic transition into amorph

253 ergents, but traditional styrene-maleic acid copolymers used for this purpose suffer severely from bu

254 Random amino acid copolymers used in the treatment of multiple sclerosis i

255 ropillar arrays, produced from cyclic olefin copolymer using high-fidelity microfabrication, as templ

256 hacrylate)-poly(methacrylic acid) tetrablock copolymer vesicles using polymerization-induced self-ass

257 d calcite crystals using model anionic block copolymer vesicles.

258 cement in thermal properties of the branched copolymer was observed, as the T(g) value increased by 2

259 The block copolymer was synthesized and characterized by nuclear m

260 The copolymer was synthesized via the condensation of N,N-di

261 er and cellular uptake of PMeOzi- grad-PBuOx copolymers was confirmed in vitro in SKOV3 cells.

262 ly(ethylene oxide)-b-poly(butadiene) diblock copolymer, we show that membrane protein folding and pro

263 s affecting the extraction efficiency of the copolymer were optimized.

264 y, PLA-b-PEG400-N(3) and PLA-b-PEG2000 block copolymers were bound to adenosine at the 3',4'-OH, 5'-O

265 r mass polyethylene and ethylene-co-1-octene copolymers were separated with high efficiency.

266 imethylacrylamide/4-acryloylmorpholine block copolymers were synthesized and analyzed by electron cap

267 ammonium-functionalized amphiphilic diblock copolymers were synthesized and blended with a PVDF/grap

268 can be tuned through the composition of the copolymers, where two different monomers with the same c

269 synthetic polymeric vehicle from a triblock copolymer which encapsulates exosomes by polymeric self-

270 f FDA-approved amphiphilic triblock Pluronic copolymers which act as gelling agents.

271 inctive molecular architecture, ABA triblock copolymers will undergo specific self-assembly processes

272 A cathepsin B/pH dual-sensitive block copolymer with a molecular weight of 92 kDa was synthesi

273 We report the design of a diblock copolymer with architecture and function inspired by the

274 ching from the E to Z isomer of m-BTA in the copolymer with inert a-BTA.

275 The triblock copolymer with one vitamin E molecule on each end of PEG

276 report a novel poly(2-oxazoline)-based block copolymer with the aromatic heterocyclic side chains in

277 ns to produce high molecular weight aromatic copolymers with 1,1-disubstituted alkene backbone linkag

278 ation, which autonomously propagates to form copolymers with alternate tile units.

279 norbornene-based (macro)monomers to provide copolymers with backbone degradability under mildly acid

280 s of vitamin E-functionalized 'ABA' triblock copolymers with carbamate block junction, which can form

281 m fiber-like nanoparticles from PLLA diblock copolymers with controlled lengths up to 1 mum can be pr

282 nzoladderenes yielded homopolymers and block copolymers with controlled molecular weights and low dis

283 In this seeded growth strategy, block copolymers with crystallizable core-forming blocks and f

284 esize linear, bottlebrush and brush-arm star copolymers with degradable segments.

285 a the sequential seeded-growth of PLLA block copolymers with different corona-forming blocks.

286 emplified by synthesis of well-defined block copolymers with distinct branching characteristics per b

287 ter and polycarbonate homopolymers and block copolymers with exquisite efficiency and control.

288 Experiments have revealed that diblock copolymers with insufficient conformational asymmetry to

289 Salt-doped diblock copolymers with microphase-separated domains of both an

290 c-9-en-1-yloxy)silane give the corresponding copolymers with no decrease in activity.

291 r the preparation of homopolymers or diblock copolymers with perfect stereoselectivity, narrow disper

292 The reflectins are block copolymers with repeated canonical domains interspersed

293 te interactions of the zwitterion-containing copolymers with the PNPs induce dispersed or weakly aggr

294 and their use to access triblock amphiphilic copolymers with the PP block located in the center is de

295 In this report, we merge block copolymers with vitrimers in an effort to realize the pr

296 The resulting copolymers, with alternating hydrophilic linear and hydr

297 this single monomer, cis-trans-cis triblock copolymers, with potential applications as thermoplastic

298 lycol)-b-poly(d,l-lactide) (PEG-PDLLA) block copolymers, with the two blocks connected via a pH sensi

299 on of antibiotic and phase separation of the copolymers within the polymerizing/hardening of the ceme

300 introduced zwitterionic styrene-maleic amide copolymers (zSMAs) to overcome this limitation.