ライフサイエンスコーパス: copolymer

1 used to estimate the backbone shape for each copolymer.

2 lene glycol)-b-poly(l-glutamic acid) diblock copolymer.

3 attractive to both blocks of the underlying copolymer.

4 h the polymerization of an amphiphilic block copolymer.

5 lymerization to produce a "self-plasticized" copolymer.

6 on efficiency of 8.4% is a record for a DARP copolymer.

7 enhances formation of a functional Drp1-Mff copolymer.

8 ed access to a series of four donor-acceptor copolymers.

9 ene glycol)-bl-poly(propylene sulfide) block copolymers.

10 stallization-driven self-assembly of diblock copolymers.

11 eld semiconducting polyacetylene-based block copolymers.

12 ted N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers.

13 h as monodisperse PFS homopolymers and block copolymers.

14 nt detectable structural defects in the DARP copolymers.

15 ed to rationally guide the assembly of block copolymers.

16 ling dendrons but often encountered in block copolymers.

17 f a series of ultra-pH sensitive (UPS) block copolymers.

18 pects for entirely new applications of block copolymers.

19 e (VDF) and for the synthesis of their block copolymers.

20 chemical reaction to the synthesis of block copolymers.

21 e almost instantaneously on solvation of the copolymers.

22 hynylene)-block-poly-(methyl acrylate) block copolymers.

23 ecular weights and architecture of the block copolymers.

24 nanostructures assembled from rod-coil block copolymers.

25 ture and composition of these supramolecular copolymers.

26 n process in ultralow-molecular-weight block copolymers.

27 embly of solid-core nanoparticles from block copolymers.

28 t system for the convenient synthesis of the copolymer, a cross-linkable PE.

29 Micelles prepared from amphiphilic block copolymers (ABCs) have found numerous applications in ph

30 The copolymer acts as a stimuli-responsive anchor that can b

31 Styrene-maleic acid copolymers allow for solubilization and reconstitution o

32 Temperature-induced self-assembly of block copolymers allows the formation of smart nanodimensional

33 to determine these critical conditions in a copolymer, alongside the inevitable chemical composition

34 The Gadolinium-chelated HPMA copolymers also showed significant enhancement in accumu

35 In contrast, experimental studies on block copolymers always employ materials with disperse molecul

36 was composed of a strongly segregated block copolymer, an intermediately segregated gradient copolym

37 blend between a donor-acceptor polyfluorene copolymer and a fullerene derivative.

38 tion of poly [pyrrole-co-3-carboxyl-pyrrole] copolymer and aptamer for the development of a label-les

39 d growth of crystallizable blends of a block copolymer and homopolymer yields well-defined, low area

40 ers of a hydrophobic, perfluorinated acrylic copolymer and hydrophobic surface functional silicon dio

41 employed to modify an oxime-bearing styrene copolymer and introduce an array of polar functionalitie

42 one-pot synthesis of an amphiphilic di-block copolymer and retention of oscillatory behavior for the

43 of the poly [pyrrole-co-3-carboxyl-pyrrole] copolymer and subsequently on its electrical properties.

44 h layered structure such as membranes, block copolymers and smectics exhibit intriguing morphologies

45 addition of blends of crystalline-coil block copolymers and the corresponding crystalline homopolymer

46 lymer, an intermediately segregated gradient copolymer, and a non-segregated homopolymer.

47 /polybutylene terephthalate (PEOT/PBT) block copolymer, and polysulfone.

48 provides well-defined homopolymers, diblock copolymers, and biohybrids under automated photomediated

49 -poly(ethylene oxide) (PEO-PPO-PEO) triblock copolymers, and their subsequent fabrication into polyro

50 hosis' into comb, star and hydrophobic block copolymer architectures.

51 s, polarity, and coordination effects of the copolymer are found to be the main factors affecting the

52 The mechanical properties of the copolymer are suitable for the fabrication of plasticize

53 Two different nonfullerene acceptors and one copolymer are used to fabricate ternary organic solar ce

54 The DARP-derived copolymers are benchmarked versus Stille-derived counter

55 Amphiphilic diblock copolymers are known to self-assemble in water to form a

56 nisotropic nanoparticles prepared from block copolymers are of growing importance as building blocks

57 A range of copolymers are prepared and their electrical properties

58 g this DARP protocol, several representative copolymers are synthesized in excellent yields and high

59 The random copolymers are thermoresponsive in aqueous solution, wit

60 ock-poly(ethylene oxide) (PAA-b-PEO) diblock copolymer as nanoreactor, imparting the solubility of UC

61 (CCTO) as filler and P(VDF-TrFE) 55/45 mol.% copolymer as the matrix by combining solution-cast and h

62 mers during the synthesis of homo- and block copolymers as the stability and reactivity of the carbon

63 elease of vancomycin, (iii) Eudragit E100 (a copolymer based on dimethylaminoethyl methacrylate, buty

64 over the morphology and dimensions of block copolymer (BCP) micelles has attracted interest due to t

65 plate to direct the crystallization of block copolymer (BCP) poly(ethylene oxide)-b-poly(4-vinylpyrid

66 e, an ink-jet printable and rewritable block copolymer (BCP) SC display is demonstrated, which can be

67 embly (DSA) of the domain structure in block copolymer (BCP) thin films is a promising approach for s

68 (PS)-b-polymethyl methacrylate (PMMA) block copolymers (BCP)) using either ultralow energy cesium or

69 the phase segregation of unimolecular block copolymers (BCPs) are limited by a lack of reliable, ver

70 Directed self-assembly (DSA) of block copolymers (BCPs) has been a recently demonstrated appro

71 of hydrophobic MNPs, free amphiphilic block copolymers (BCPs), and AuNPs tethered with amphiphilic B

72 ion of metal-organic cages (MOCs) into block copolymers (BCPs).

73 ric polymers, especially PVDF and PVDF-based copolymers/blends as potential components in dielectric

74 Here, we report on a random copolymer brush surface - poly(CBMAA-ran-HPMAA) - provid

75 ultra-low-fouling carboxybetaine polymer and copolymer brushes (pCB) as well as conventional carboxy-

76 efficiently with butadiene to stereoregular copolymers by [(mesitylene)Ni(allyl)][BAr(F)4] (Ni-1).

77 ort the synthesis of Janus bottlebrush block copolymers by graft-through polymerization of branched d

78 way to prepare cubic nanoparticles of block copolymers by self-assembly from aqueous solutions at ro

79 e soft-rigid molecular structure of triblock copolymers can accommodate a high loading of fillers wit

80 We also demonstrate that A-alt-B copolymers can be modified to give new variations which

81 The lattice structure of the block copolymers can be transferred to the shape of the partic

82 ved cholesterol egress, while Pluronic block copolymers capable of micelle formation showed slight ef

83 ned with ultra-low-fouling brushes of random copolymer carboxybetaine methacrylamide (CBMAA) and N-(2

84 nd so reducing the packing parameter for the copolymer chains.

85 alcohol, and amine nucleophiles onto diblock-copolymer-coated surfaces are chemoselective for the pla

86 o2(CO)6]x-EO800-PESn[Co2(CO)6]x ABA triblock copolymer/cobalt adducts (10-67 wt % PEO) were subsequen

87 ospheres composed of hydrophilic multi-block copolymers composed of poly(l-lactide) and poly ethylene

88 excellent control over molecular weight and copolymer composition.

89 We report supramolecular AB diblock copolymers comprised of well-defined telechelic building

90 t affect the tumor targeting ability of HPMA copolymer conjugates.

91 ent N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer conjugates.

92 olymers, non-covalent analogues of synthetic copolymers, constitute a new and promising class of poly

93 For example, copolymers containing 0.23 mol % silane can be generated

94 gelation behavior of a class of ABA triblock copolymers containing a central poly(ethylene oxide) blo

95 poration from micellar solutions of triblock copolymers containing a central poly(ethylene oxide) blo

96 controlled length from pi-conjugated diblock copolymers containing a crystalline regioregular poly(3-

97 Expanding on this design motif, copolymers containing the dithiopheneindenofluorene repe

98 hat the presence of 10v/v% of a linear graft copolymer could extend ibuprofen release over three-fold

99 ng gelatin and Poloxamer 188-grafted heparin copolymer demonstrated significant apoptotic and cytotox

100 direct comparison between two cationic block copolymers demonstrating the effect of polymer structure

101 ioelectronics applications using a series of copolymer derivatives based on poly(3-hexylthiophene) ar

102 n of perfectly alternating and regioslective copolymers derived from the copolymerization of carbonyl

103 descriptions of the phase behavior of block copolymers describe the chain ensembles of perfect and u

104 The rheological behavior of a 10 % w/w copolymer dispersion in mineral oil is strongly temperat

105 However, current styrene-maleic acid copolymers display severe limitations in terms of buffer

106 ble N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer-drug conjugates.

107 ing from self-assembly of mostly amphiphilic copolymers either as 3D compartments (polymersomes, PICs

108 nding H2-evolution electrode consisting of a copolymer-embedded cobaloxime integrated into a multiwal

109 f phase-separated PE and iPP with tetrablock copolymers enables morphological control, transforming b

110 d by coating instead with an oligolysine-PEG copolymer, enabling up to a 1,000-fold protection agains

111 For example, 2nd generation HPMA copolymer-epirubicin (EPI) conjugates (2P-EPI) demonstra

112 The resultant polyacetylene block copolymers exhibit long conjugation length and uniform t

113 The CPDS copolymer exhibited a band gap of just 1.18 eV, which is

114 The copolymer exhibited greater than 99% carbonate linkages,

115 es 4a,b/B(C6F5)3 yield high molecular weight copolymers exhibiting highly branched to nearly linear b

116 chlorinated solvents, with the CPDS and IDSe copolymers exhibiting hole mobility up to 0.15 and 6.4 c

117 d stack lengths of the formed supramolecular copolymers existing at various feed ratios of the two mo

118 r work is to develop, a cationic amphiphilic copolymer for simultaneous delivery of drug and therapeu

119 PFS block copolymers form phase-separated iron-rich, redox-active

120 In contrast, mPEG-b-PMTEGE block copolymers formed well-defined micelles (Rh approximatel

121 tion method enables the preparation of block copolymers from monomers with similar and competitive re

122 rchitectures, e.g. block copolymers or graft copolymers, from defined building blocks.

123 ylene over 4 h with a productivity of 560 kg copolymer/g Ni.

124 gned with the cooperation of two amphiphilic copolymer gates.

125 or example, the solution processing of block copolymers generally follows a separate synthesis step a

126 that the -CHF2 and -CH2 F chain ends in E/VF copolymer generated by (phosphinoarenesulfonate)PdR cata

127 ll-defined architectures thereof, e.g. block copolymers, graft copolymers or chain end functionalized

128 The attachment of copolymers greatly affects their dispersibility in diffe

129 CLRP-controlled synthesis of block copolymers has been applied in heterogeneous systems, mo

130 ock-poly(lactic-co-glycolic acid) (PEG-PLGA) copolymers have been used successfully for targeted deli

131 Precise PLLA-b-PDLA diblock copolymers having block lengths of up to 500 repeat unit

132 micelles based on common pi-conjugated block copolymers highlights their significant potential to pro

133 hyl methacrylate/methacrylic acid (HEMA/MAA) copolymer hydrogels as functions of composition, equilib

134 Copolymer hydrophobic/hydrophilic balance and presence o

135 MC concentration, MC salt release, copolymer hydrophobic/hydrophilic balance, and presence

136 mbranes depend on the weight fraction of the copolymer impregnated inside the tissue paper.

137 f the self-assembly of the sequence-designed copolymer in the confined geometry that minimizes the fr

138 nditions, of amphiphilic, glycosylated block copolymers in aqueous solution.

139 nking of self-assembled reactive ester block copolymers in DMSO.

140 conjugates were more effective than Pluronic copolymers in generating stable, surface neutral liposom

141 and features of ethylene-vinyl acetate (EVA) copolymers in initial research and development led to co

142 atelets formed by the self-assembly of block copolymers in selective solvents are of interest for a r

143 icelles formed by the self-assembly of block copolymers in selective solvents have attracted widespre

144 rphological studies of the amphiphilic block copolymers in solution were conducted by atomic force mi

145 Self-assembly of block copolymers in solvents that selectively solvate one of t

146 ansfer and formation of low molecular weight copolymers in the traditional catalyst system, t-1.

147 ngerprint of a broad distributed statistical copolymer including MMD, FTD, CCD, and MSD.

148 -ray scattering of the thiophene-selenophene copolymers indicated that the pi-stacking distance incre

149 ion, a controlled method of assembling block copolymers into 1D or 2D structures that resembles a liv

150 stallization-driven self-assembly of diblock copolymers into cylindrical micelles of controlled lengt

151 ins can direct the assembly of protein block copolymers into physically cross-linked, viscoelastic hy

152 e amphiphiles into liposomes, and from block copolymers into polymersomes.

153 show the self-assembly of crystalline block copolymers into size-specific cylindrical micelles for t

154 A soluble copolymer is obtained by a palladium-catalyzed Stille po

155 The styrene-maleic acid (SMA) copolymer is rapidly gaining attention as a tool in memb

156 g of hollow carbon nanospheres with triblock copolymers is a promising strategy to fabricate mixed-ma

157 Directed self-assembly (DSA) of block copolymers is an emergent technique for nano-lithography

158 essibility of sequence-controlled multiblock copolymers is demonstrated by direct "in situ" polymeriz

159 polymerization of polystyrene-polyacrylamide copolymers is established.

160 ard the synthesis of well-defined PVDF block copolymers is presented.

161 tor (an indacenodithiophene-benzothiadiazole copolymer) is combined with a carefully optimized archit

162 ing benzodithiophene-alt-fluorobenzotriazole copolymer J51 as a medium-bandgap polymer donor and the

163 A library of 32 polystyrene copolymer latexes, with diameters ranging between 53 and

164 high chi-low N block molecules, where block-copolymer-like self-assembly in our UPy-functionalized o

165 Recent developments in scanning probe block copolymer lithography (SPBCL) enable the confinement of

166 re synthesized by using scanning probe block copolymer lithography and characterized using correlated

167 ppropriate cations, well-defined alternating copolymers made of CO2 and propylene oxide (PO) or cyclo

168 sly achieved by grafting amphiphilic diblock copolymers made of sequence-controlled hydrophobic and i

169 Among the series, the block copolymer maximized both protein binding and translocati

170 orming poly(isoprene-b-lactide) (IL) diblock copolymer melt, investigated as a function of time follo

171 enzymes deposited on top of a semipermeable copolymer membrane and outer polyurethane layers.

172 nanodiscs, i.e., discoidal amphiphilic block copolymer membrane patches encased within membrane scaff

173 r mechanical and chemical stability of block copolymer membranes and their chemical versatility for a

174 he evolution of individual amphiphilic block copolymer micellar nanoparticles in solution, in real ti

175 Cylindrical block copolymer micelles have shown considerable promise in va

176 Patchy block copolymer micelles with a corona consisting of two chemi

177 o seeds generated by the sonication of block copolymer micelles with crystalline cores yields uniform

178 or example, nanoemulsions, drug-loaded block-copolymer micelles, and nanocrystal-core reconstituted h

179 rated in the hydrophobic core of amphiphilic copolymer micelles, and was used to coordinate with bioc

180 ilms based on monodisperse cylindrical block copolymer micelles.

181 Aniline-based copolymer, modified with the nanomaterials, allowed to e

182 eering an asymmetric, biodegradable triblock copolymer molecule comprising hydrophilic, hydrophobic,

183 the spontaneous interfacial self-assembly of copolymer molecules on biopolymer coacervate microdrople

184 The evolution in copolymer morphology (and the associated sol-gel transit

185 Random and block mPEG-b-PMTEGE copolymers (Mw/Mn = 1.05-1.17) were obtained via anionic

186 hree cyclopentadithiophene-difluorophenylene copolymers (named PhF2,3, PhF2,5, and PhF2,6), which dif

187 Polydiacetylene (PDA) and triblock copolymer nanoblends were synthesized to detect micellar

188 filtering can be implemented into one single copolymer nanogate.

189 ly(benzyl methacrylate) [PSEM-PBzMA] diblock copolymer nanoparticles can be prepared with either a hi

190 lts contribute to future applications of PDA/copolymer nanosensors to dairy models.

191 conjugate DCL or AG to obtain the respective copolymers, needed for the preparation of targeted NPs.

192 a family of photo-curable methacrylate based copolymer networks.

193 Supramolecular copolymers, non-covalent analogues of synthetic copolyme

194 with the polymer donor PBFTAZ (model system; copolymer of benzo[1,2-b:4,5-b']dithiophene and 5,6-difl

195 ethylene ether carbonate) (PEEC), which is a copolymer of ethylene oxide and ethylene carbonate, was

196 Specifically, a linear precursor copolymer of styrene and 4-(diphenylphosphino)styrene wa

197 of designing tumor-pH-labile linkage-bridged copolymers of clinically validated poly(D,L-lactide) and

198 The self-assembly of amphiphilic copolymers of controlled architecture in supercritical c

199 gth of a multicatenane copolymer relative to copolymers of cyclic and linear analogs.

200 ethylene oxide (EO) and propylene oxide (PO) copolymers of different monomer compositions and differe

201 First, triblock copolymers of PEG-CNA-PLGA are synthesized and then form

202 Colorless and highly transparent copolymers of poly(monothiocarbonate) were successfully

203 g this technique, a linear amphiphilic block copolymer or hyperbranched polymer undergoes 'metamorpho

204 compared with traditional surfactant, block copolymer or metal-organic framework linkers.

205 ctures thereof, e.g. block copolymers, graft copolymers or chain end functionalized assemblies.

206 tly linked polymer architectures, e.g. block copolymers or graft copolymers, from defined building bl

207 s and corresponding isomeric NBA-bithiophene copolymers P1 and P2, respectively, reveals the key role

208 For the DARP copolymer PBDTT-FTTE, the power conversion efficiency of

209 ith polycation, then coated by anionic block copolymer, PEG-polyglutamic acid (double-coat (DC) nanoz

210 eory expose close analogies to ABA' triblock copolymer phase behavior, collectively suggesting that l

211 hologies that are absent in the native block copolymer phase diagram.

212 s, useful to study the lower limits of block copolymer phase segregation in detail.

213 We use poly(lactide-co-glycolide) copolymer (PLGA) fiber microfilaments as a floating scaf

214 allizable blend of the latter with the block copolymer PLLA42-b-P2VP240, respectively.

215 After being encapsulated with biodegradable copolymer pluronic F-127-folic acid (F-127-FA), RET-BDP

216 Liposome modification with PEG copolymers (Pluronics), phospholipid-PEG conjugates and

217 /individual multi-arm star amphiphilic block copolymer poly(amidoamine)-polyvalerolactone-poly(ethyle

218 al polymersomes comprising the biodegradable copolymer poly(ethylene glycol)-b-poly(d,l-lactide) into

219 lyion condensation with a conventional block copolymer poly(ethylene glycol)-b-poly(L-lysine) (PEG-PL

220 Copolymer poly(lactic-co-glycolic acid) (PLGA) nanoparti

221 d characterization of a cationic amphiphilic copolymer, poly (lactide-co-glycolide)-graft-polyethylen

222 re by amphiphilic poly(ionic liquid) diblock copolymers, poly(acrylic acid)-block-poly(4-vinylbenzyl)

223 polyesters such as polylactide (PLA) or its copolymer, polylactide-co-glycolide (PLGA), do not allow

224 Amphiphilic star-like triblock copolymers [polystyrene-block-poly(acrylic acid)-block-p

225 traction (SPE) with a styrene-divinylbenzene copolymer (PPL) sorbent, which has become an established

226 dependent upon the composition of the block copolymer precursors.

227 n of both dithiolane monomers into the block copolymers provides a facile way to tailor the propertie

228 hain-end functional homopolymers and diblock copolymers, providing facile access to semi-fluorinated

229 ative mechanical strength of a multicatenane copolymer relative to copolymers of cyclic and linear an

230 ficiencies, closely followed by the gradient copolymer, resulting in two protein transporter molecule

231 mass poly(isoprene)-b-poly(lactide) diblock copolymers reveal an extraordinary thermal history depen

232 Microstructural analysis of the copolymers reveals both in-chain and chain-end incorpora

233 pproach allows the engineering of multiblock copolymer scaffolds featuring diverse secondary structur

234 n material design and application, and block copolymer self-assembly is one particularly powerful phe

235 heterogeneous routes, the incidence of block copolymer self-assembly within dispersed particles durin

236 In aqueous solution, these amphiphilic block copolymers self-assemble into bridged flower micelles at

237 To gain insight into the copolymer sequence and architecture, self-propagation an

238 PEO45 -PDEAm89 -PDBAm12 copolymer solutions, which undergo a thermally induced t

239 Lipids and amphiphilic block copolymers spontaneously self-assemble in water to form

240 r solute-specific interactions with hydrogel copolymer strands.

241 d in squid suction cups that has a segmented copolymer structure with amorphous and crystalline domai

242 ain-chain supramolecular ABC and ABB'A block copolymers sustained by orthogonal metal coordination an

243 Finally, block copolymer synthesis and catalyst recycling were demonstr

244 risation (CLRP) has greatly simplified block copolymer synthesis, and versatility towards monomer typ

245 Herein, a diblock copolymer system consisting of a hydrophilic block and a

246 we prepared nanoblends of PDA with triblock copolymers (TC) as a better sensor system for detecting

247 indium tin oxide (ITO) substrate via a block copolymer template was developed for highly sensitive an

248 ized by mixing polymer precursors with block copolymer templates, curing at 140-180 degrees C, and ca

249 continuous charge regulation of the confined copolymer that allows logical gating in biosensors and n

250 fully macromolecular FLP, built from linear copolymers that containing either a sterically encumbere

251 present a new family of styrene-maleic acid copolymers that do not aggregate at low pH or in the pre

252 in contrast to uncharged, amphiphilic block copolymers that form discrete micelles at low concentrat

253 e have designed a range of statistical graft copolymers that incorporate dimethylsiloxane and ethylen

254 y the synthesis of their parent linear block copolymers that provide monovalency, fluorescence and na

255 upper critical phase separation (UCST) block copolymers that would allow the swelling or disassembly

256 densation methods for producing photovoltaic copolymers, this DARP protocol eliminates the need for e

257 Ratcheted reciprocating motion of a DNA/PEG copolymer threaded through a single alpha-hemolysin pore

258 sive guidelines for the design of CO2-philic copolymers through an exhaustive and precise coverage of

259 r strategy gives access to amphiphilic block copolymers through synthetic cascades of ROAMP followed

260 ity and chain conformation of the star block copolymers to initiate out-of-shell release (elevated te

261 We synthesized PE/iPP multiblock copolymers using an isoselective alkene polymerization i

262 pe for the design of new stimulus-responsive copolymer vesicles (and hydrogels) for targeted delivery

263 Diblock copolymer vesicles are prepared via RAFT dispersion poly

264 oxypropyl methacrylate) (PGMA-PHPMA) diblock copolymer vesicles were prepared via aqueous polymerizat

265 ica nanoparticles) encapsulated within block copolymer vesicles.

266 can be used to synthesize well-defined block copolymers via a sequential addition strategy.

267 The copolymer was covalently modified with triazole moiety t

268 PLGA-b-PEG copolymer was synthesized and characterized by (1)H NMR,

269 col (PEG) and the delivery efficiency of the copolymer was tested in vivo for regeneration of dystrop

270 Evidence for the formation of block copolymers was obtained from solubility differences, GPC

271 HT)-block-poly(ethylene oxide) (PEO) diblock copolymers was realized using the complementary ligand p

272 yl)styrene) (PPES-b-PEO-b-PPES) ABA triblock copolymers was synthesized by reversible addition-fragme

273 g direct attachment and formation of a block copolymer were prepared and demonstrated for the separat

274 nanocarriers comprised of amphiphilic block copolymers were engineered for targeted uptake by murine

275 elf-assemble in water from amphiphilic block copolymers were investigated as aerosolized delivery veh

276 The target functional copolymers were prepared by a controlled radical copolym

277 AB diblock copolymers were prepared by encapsulating a frozen solut

278 After the copolymers were shown to be non-toxic to retinal pigment

279 Diblock copolymers were synthesized with different targeted degr

280 Cis,syndiotactic A-alt-B copolymers, where A and B are two enantiomerically pure

281 ical temperatures by an amphiphilic triblock copolymer which can emulsify PFCs and be cross-linked.

282 rylamide) (PEO45 -PDEAmx -PDBAm12 ) triblock copolymers, which differ only in the size of the central

283 Its copolymer with benzothiadiazole is an excellent p-type s

284 Block copolymers with a crystallisable PFS core-forming block

285 tical adsorption point (CPA) for statistical copolymers with a given chemical and sequence distributi

286 ers and traditional vinyl monomers to obtain copolymers with advanced properties; (iv) the different

287 ration of a series of crystallizable diblock copolymers with appropriate wettability and chemical rea

288 Copolymers with benzothiadiazole were prepared in high y

289 Both homopolymers and block copolymers with controlled molecular weights, narrow mol

290 xternal reagents) one-pot synthesis of block copolymers with conventional glassware using straightfor

291 stor consisting of modular fluorescent block copolymers with discrete and sharp pH transitions in one

292 Star block copolymers with dual-responsive blocks (temperature for

293 d styrene furnishing higher molecular weight copolymers with minimal termination.

294 oser, allowing the preparation of multiblock copolymers with ordered sequences of functional monomers

295 Block copolymers with PEG as a nonresponsive water-soluble blo

296 e construction of uniform hexamers and graft copolymers with precisely defined branches.

297 he lactide enantiomers to afford stereoblock copolymers with predetermined number and lengths of bloc

298 alizing on functional bottlebrush-like block copolymers with well-defined structures and narrow molec

299 Highly hydroxylated block copolymer worms are shown to be a suitable replacement f

300 Moreover, these block copolymer worms enable post-thaw gelation by simply warm