ライフサイエンスコーパス: polyelectrolyte

1 surface coating (e.g., choice of polymers or polyelectrolytes).

2 in its active center with negatively charged polyelectrolyte.

3 e relationship holds across a broad range of polyelectrolytes.

4 under antifouling phosphorylcholine-grafted polyelectrolytes.

5 r average size than films prepared from weak polyelectrolytes.

6 growth was observed for both linear and star polyelectrolytes.

7 rganically capped colloidal nanocrystals and polyelectrolytes.

8 r-by-layer deposition of alternately charged polyelectrolytes.

9 semble around homopolymeric RNA or synthetic polyelectrolytes.

10 e deposition of biochemically functionalized polyelectrolytes.

11 e to unintended free wrapping agents such as polyelectrolytes.

12 r deposition of positive or negative charged polyelectrolytes.

13 olymers depends on (inter)diffusion of these polyelectrolytes.

14 ontacts via the self-assembly of these doped polyelectrolytes.

15 stems including nanoparticles, colloids, and polyelectrolytes.

16 rol cell membrane structures with conductive polyelectrolytes.

17 Dialysis experiments show that, for a 15 kDa polyelectrolyte, a 50 kDa dialysis membrane is not suffi

18 ricated from two types of optically quenched polyelectrolytes, a life indicator and a death indicator

19 rbing cellulosic fibers, functionalized with polyelectrolytes according to the layer-by-layer method,

20 tration (CAC) of surfactants is lowered when polyelectrolytes act as counterions.

21 primary exciton lifetime is shortened in the polyelectrolyte and a red-shifted CT emission peak with

22 to study the intermolecular interactions in polyelectrolyte and bio-macromolecular solutions.

23 sensors by inkjet printing the LbL layers of polyelectrolyte and enzyme on paper is demonstrated.

24 n the progress of using conducting polymers, polyelectrolyte and its composites (co-polymer, carbonac

25 Swelling behavior of polyelectrolyte and polyzwitterion brushes derived from

26 ction layers combining pH-neutral conjugated polyelectrolytes and a thin film of ZnO nanoparticles by

27 icrodroplets prepared from cationic peptides/polyelectrolytes and adenosine triphosphate or oligo/pol

28 hrough a layer-by-layer assembly of cationic polyelectrolytes and amplicons.

29 on of polyferrocenylsilane diblock copolymer polyelectrolytes and AOT-based surfactants, is described

30 assembly of metal-containing block-copolymer polyelectrolytes and azobenzene chromophores is exploite

31 by layer-by-layer deposition of proteins and polyelectrolytes and by encapsulating polymers into prot

32 us histone tails using ideas from physics of polyelectrolytes and disordered systems.

33 e adverse effects of the deposited polymers, polyelectrolytes and nanoparticles on the cell surface.

34 lecules, mixed cationic-anionic surfactants, polyelectrolytes and other polymers, micropatterned self

35 be feasible in other biosensors based on the polyelectrolytes and sandwiched enzymes providing that a

36 id carriers based on assembled biodegradable polyelectrolytes and sol-gel coating possess several adv

37 lence provides new insights into theories of polyelectrolytes and the biological and pathological rol

38 ories of the electrostatics of surface-bound polyelectrolytes and the entropy of surface-bound polyme

39 amental insight into the dynamics of charged polyelectrolytes and the solvating water molecules.

40 ectronvolts), by charge-doping of conjugated polyelectrolytes and then internal ion-exchange to give

41 solutes [small mono- and multicharged ions, polyelectrolytes, and organic/inorganic (nano)particles]

42 atechol functionalization of polymers and/or polyelectrolytes, and solution processing of many comple

43 ologically derived polysaccharides behave as polyelectrolytes, and their polyelectrolyte nature can b

44 Conjugated polyelectrolyte-antibody hybrid materials promise to enh

45 ght into phenomena more generally underlying polyelectrolyte applications in the chemical, environmen

46 n is achieved by using a stimulus-responsive polyelectrolyte-aptamer thin film to control the rate of

47 Threose nucleic acid (TNA) and other polyelectrolytes are also considered as the possible fir

48 lt on a silicone sheet and where RGD-grafted polyelectrolytes are embedded under antifouling phosphor

49 These polyelectrolytes are freely soluble in water and display

50 hat while nanoparticles prepared with longer polyelectrolytes are more stable under simulated physiol

51 engineering based mainly on the assembly of polyelectrolytes are reviewed.

52 m weak polyelectrolytes shows that when both polyelectrolytes are substantially charged in solution (

53 Polyelectrolytes are used to electrostatically assemble

54 Because excess polyelectrolytes are usually employed in the surface mod

55 By introducing an amphiphilic conjugated polyelectrolyte as an interfacial compatibilizer, fabric

56 -temperature solution-processable conjugated polyelectrolyte as the hole transport layer (instead of

57 ormed using layer by layer (LbL) assembly of polyelectrolytes as a model system.

58 ess the glass transition temperature (Tg) of polyelectrolyte assemblies at solid-electrolyte interfac

59 lt ions and polyelectrolyte, the strength of polyelectrolyte association is described by a single uni

60 ombic interactions which support theories of polyelectrolyte association rooted in continuum electros

61 The physical behavior of polyelectrolytes at solid-liquid interfaces presents cha

62 ed by the complexation of oppositely charged polyelectrolytes at the immiscible interface.

63 illustrate that weak bonding interactions in polyelectrolyte-azobenzene surfactant mesophases can be

64 the development of a new class of functional polyelectrolytes based on the aromatic cyclopropenium io

65 of benzyl methacrylate in alcohol using weak polyelectrolyte-based chain transfer agents allows the f

66 an efficient way to produce well-controlled polyelectrolyte-based nanoparticles suitable for colloid

67 nd consider how this may be applied to other polyelectrolyte-based systems as a general method for su

68 To date, most cationic polyelectrolytes bear charge formally localized on heter

69 4; 2) high-anionic-content Nanodiscs exhibit polyelectrolyte behavior; 3) 3 mM Ca(2+) neutralizes a c

70 vel underpinnings that distinguish an active polyelectrolyte binder designed for lithium-sulfur batte

71 In this work, a polyelectrolyte binder, SiO2 nanoparticles, and a fluoro

72 Polyelectrolyte binder, SiO2 nanoparticles, and silane o

73 (Rct) of a redox probe diffusing through the polyelectrolyte brush was measured, and the temperature

74 hick fuzzy coat that resembles a two-layered polyelectrolyte brush, which is formed by the unstructur

75 e the glass transition temperature of planar polyelectrolyte brushes at solid-liquid interfaces.

76 charge repulsion is found in weak or strong polyelectrolyte brushes.

77 tforward proposal that counterions bind to a polyelectrolyte by distributing themselves randomly into

78 E, molar mass distribution of evenly charged polyelectrolytes by CGE, and charge density distribution

79 ge density distribution of variously charged polyelectrolytes by free solution CE.

80 We found that a polycationic polyelectrolyte can penetrate through the Au overlayer t

81 These triblock polyelectrolytes can also be used as interfacial layers

82 Further, sulfonium PEG polyelectrolytes can be obtained via alkylation or alkox

83 ow the optomechanical response of conjugated polyelectrolytes can be used to detect their encapsulati

84 lectrokinetics of soft particles: a layer of polyelectrolyte (cationic on one electrode, anionic on t

85 Other nanoparticle polyelectrolyte cations may be anticipated.

86 e molecules) for the behavior of hydrophobic polyelectrolyte chains adsorbed at a solid-liquid interf

87 on-diffusion ranges of positive and negative polyelectrolyte charge lead to a blanket of glassy, stoi

88 ed of SN-AZU, carbon nanotubes, and cationic polyelectrolyte chitosan.

89 ce chemical gradient created by differential polyelectrolyte coating of the paper.

90 this adaptive release system, we applied the polyelectrolyte coating on a well-studied biodegradable

91 wn in anodized aluminum oxide membranes with polyelectrolyte coatings to modify the surface charge.

92 Living cells interfaced with a range of polyelectrolyte coatings, magnetic and noble metal nanop

93 roximately 6%) is considerably lower for the polyelectrolyte compared with F8BT (approximately 60%) i

94 ygenase was immobilised in the form of solid polyelectrolyte complex gel membrane made of cellulose s

95 Polyelectrolyte complex microcapsules are prepared using

96 -HPA) hydrogels and dextran sulfate/chitosan polyelectrolyte complex nanoparticles (PCNs) that delive

97 Thin films of polyelectrolyte complex were assembled using the multila

98 balanced by counterions-within thin films of polyelectrolyte complex, PEC, using sensitive isotopic l

99 Polyelectrolyte complexation is critical to the formatio

100 -contact microporous adhesive resulting from polyelectrolyte complexation triggered by solvent exchan

101 phase of individual micelles is prevented in polyelectrolyte complexation-driven assembly of triblock

102 tool for manipulating material properties in polyelectrolyte complexation.

103 Polyelectrolyte complexes (PEC) are formed by mixing the

104 Polyelectrolyte complexes are examples of a broader clas

105 fewer kinetic limitations on the assembly of polyelectrolyte complexes in all of their forms.

106 d on the formation of insoluble nanoparticle-polyelectrolyte complexes of various compositions provid

107 plify and accelerate the characterization of polyelectrolyte complexes or polyplexes.

108 Polyelectrolyte complexes present new opportunities for

109 trate that chirality determines the state of polyelectrolyte complexes, formed from mixing dilute sol

110 nalysis was used for the characterization of polyelectrolyte complexes.

111 ermore, we report the finding that synthetic polyelectrolytes composed of an aromatic sulfonic acid b

112 siveness to environmental stimuli by varying polyelectrolyte composition.

113 s were converted into nanosized complexes by polyelectrolyte condensation to manipulate their physico

114 ometry and the hydrodynamic radii of the two polyelectrolyte constituents were determined in a fully

115 ssociation and electrophoretic separation of polyelectrolyte constituents.

116 In addition, this polyelectrolyte could serve successfully as reaction med

117 between photoluminescent anionic conjugated polyelectrolyte (CPE) bound captureprobe coated onto mag

118 Our investigation is focused on a conjugated polyelectrolyte (CPE) derived from F8BT (poly(9,9'-dioct

119 .5% by incorporating an ultrathin conjugated polyelectrolyte (CPE) layer between the active layer and

120 film transistors (OTFTs), a thin conjugated polyelectrolyte (CPE) layer was interposed between elect

121 erties and function of an anionic conjugated polyelectrolyte (CPE)-containing ion-conducting polyethy

122 The interfaces of conjugated polyelectrolyte (CPE)/poly[2-methoxy-5-(2'-ethylhexyloxy

123 Conjugated polyelectrolytes (CPEs) are versatile materials used in

124 nionic narrow-band-gap self-doped conjugated polyelectrolytes (CPEs) with pi-conjugated cyclopenta-[2

125 on of bacteria in the presence of conjugated polyelectrolytes (CPEs).

126 The adsorbed polyelectrolytes create a positive charge on the fiber s

127 l junction) consisting of bilayer conjugated polyelectrolyte, demonstrating an unprecedented PCE of 1

128 ied out to investigate the local dynamics of polyelectrolyte dendrimers dissolved in deuterium oxide

129 d by electrostatic self-assembly of cationic polyelectrolyte dendrimers of different generations and

130 of oppositely charged polyelectrolytes into polyelectrolyte dense (coacervate) and polyelectrolyte d

131 into polyelectrolyte dense (coacervate) and polyelectrolyte dilute (supernatant) phases.

132 ostatic attraction is solely responsible for polyelectrolyte-directed intrafibrillar mineralization.

133 y to establish Gibbs-Donnan equilibrium in a polyelectrolyte-directed mineralization system establish

134 otein sequences are disordered, and that two polyelectrolyte domains within each protein contribute t

135 es may also control the function of Asp, Glu polyelectrolyte domains within other IDP proteins.

136 d proteins, particularly those which possess polyelectrolyte domains, represent potential members of

137 pected for nonspecific binding driven by the polyelectrolyte effect.

138 free energy contributions demonstrates that polyelectrolyte effects account for half of the total fr

139 ovide a framework for understanding flexible polyelectrolyte elasticity across a broad range of relat

140 p that connects side chain structure (polar, polyelectrolyte, etc., number of ionic groups per repeat

141 ectroelectrochemical sensor uses thin, solid polyelectrolyte films as an essential element in its ope

142 nalize the temperature-dependent behavior of polyelectrolyte films in a wide range of settings.

143 he rest potential and structural response of polyelectrolyte films to salt concentration.

144 mposites formed via impregnation of hydrated polyelectrolyte films with binary water/alcohol solution

145 anoparticle catalysts embedded in multilayer polyelectrolyte films.

146 rolytes makes these films tend toward weaker polyelectrolyte free volume characteristics.

147 In the case of polyelectrolytes, free-solution capillary electrophoresi

148 imentally guided, multi-phase, multi-species polyelectrolyte gel model to make qualitative prediction

149 RNA to be covalently attached to a swellable polyelectrolyte gel synthesized throughout a biological

150 d by embedding them in a densely crosslinked polyelectrolyte gel, anchoring key labels or biomolecule

151 ical conditions, those prepared with shorter polyelectrolytes have a higher antimicrobial activity.

152 Films assembled from strong polyelectrolytes have fewer free volume cavities with a

153 Polyelectrolytes have proven their advantages as draw so

154 hrough the addition of either a like charged polyelectrolyte homopolymer or through careful control o

155 sponsive cryogels can be reproduced in other polyelectrolyte hydrogel systems to fabricate biomimetic

156 ronment found in cartilage is achieved using polyelectrolyte hydrogels based on polyvinyl alcohol and

157 prepared from strong polyelectrolytes, weak polyelectrolytes, hydrogen-bonding polymers, and blended

158 = 7.5), the chains pack similarly to strong polyelectrolytes (i.e., lower free volume concentration)

159 The modification of rGO FETs with a weak polyelectrolyte improved the pH response because of its

160 lized to rationalize the complex behavior of polyelectrolytes in aqueous solution.

161 ransparent, and colorful LbL films from star polyelectrolytes in contrast to mostly heterogeneous fil

162 on of the binding strength of surfactants to polyelectrolytes in salt-free mixtures as a function of

163 umina powder and nanoparticles stabilized by polyelectrolytes in solution.

164 lly coated capillary were found to avoid any polyelectrolyte interactions onto the capillary surface.

165 ative phase separation of oppositely charged polyelectrolytes into polyelectrolyte dense (coacervate)

166 The translocation dynamics of polyelectrolytes is of particular interest given potenti

167 tte modified in the tip region with cationic polyelectrolytes is presented with an unpurified PCR pro

168 The binder, a cationic polyelectrolyte, is shown to both facilitate lithium-ion

169 widely employed pair of "linearly" assembled polyelectrolytes it was found that the accepted model of

170 with silver ions and coated with a cationic polyelectrolyte layer form a biodegradable and green alt

171 The first polyelectrolyte layer is inserted through the titania me

172 The polyelectrolyte layer promotes the adhesion of the parti

173 the low-bandgap material after using a thin polyelectrolyte layer to modify the electron-transport Z

174 e PCL fibrous substrate were established via polyelectrolyte layer-by-layer deposition, which was inv

175 ing metric of the equilibrium structure of a polyelectrolyte layer.

176 d to the film surface by a varying number of polyelectrolyte layers.

177 sub-millimeter architectures with submicron polyelectrolyte layers.

178 1)) and carboxymethylcellulose (CMC, anionic polyelectrolyte, M.W. 700000 g mol(-1)) on TCE degradati

179 we report the high-resolution deposition of polyelectrolyte macroinitiators and subsequent polymer b

180 nanoscale devices comprising a monolayer of polyelectrolyte macromolecules.

181 ion solutions for films prepared from strong polyelectrolytes makes these films tend toward weaker po

182 y engineered Escherichia coli immobilised in polyelectrolyte membrane onto a miniaturised oxygen elec

183 y due to the unique swelling behavior of the polyelectrolyte membrane.

184 es that rely on the use of proton-conducting polyelectrolyte membranes is the lack of control over th

185 strated the feasibility of using regenerable polyelectrolyte membranes to ultimately control the irre

186 Nanoporous polyelectrolyte membranes with hierarchical and unique p

187 The all-polysaccharide based polyelectrolyte microcapsules combining copigmentation f

188 fluidic approach for one-step fabrication of polyelectrolyte microcapsules in aqueous conditions.

189 plets and use them as templates to fabricate polyelectrolyte microcapsules.

190 observed in cationic surfactant and anionic polyelectrolyte mixtures.

191 Consistent with predictions from polyelectrolyte models, we observed logarithmic dependen

192 A polyelectrolyte multilayer (PEM) approach using alginate

193 Layer-by-layer assembly of polyelectrolyte multilayer (PEM) films represents a bott

194 stituted of a Love wave sensor coated with a polyelectrolyte multilayer (PEM).

195 so extended to a more practically applicable polyelectrolyte multilayer adsorbate system.

196 ms such as ultrathin films, polymer brushes, polyelectrolyte multilayer assemblies, ultrasoft materia

197 s technique, we explore issues common to the polyelectrolyte multilayer field, such as the competitio

198 ith visible light, the emission color of the polyelectrolyte multilayer film appears orange due to FR

199 bricated by first generating a highly porous polyelectrolyte multilayer film of poly(acrylic acid) an

200 eory and the mechanism of charge transfer in polyelectrolyte multilayer films (PEM), as well as betwe

201 This mechanoresponsive surface is based on polyelectrolyte multilayer films built on a silicone she

202 Free-standing, stimuli-responsive polyelectrolyte multilayer films enabled by light-induce

203 ve to negative polymer repeat units within a polyelectrolyte multilayer made from poly(diallyldimethy

204 oly(ether sulfone) (PES) membranes using the polyelectrolyte multilayer modification method with poly

205 An initial filtration test showed that polyelectrolyte multilayer modified cellulosic fibers ca

206 ar array on a glass surface that possessed a polyelectrolyte multilayer patterned through inkjet prin

207 enhance the understanding of how to control polyelectrolyte multilayer structure, what chemical comp

208 tamide (MPA) of ampicillin was adsorbed into polyelectrolyte multilayer surface coatings composed of

209 These structures are compared with polyelectrolyte multilayers (PEM) thin films having arra

210 bromotyrosine (Br(2)Y) and chitosan-alginate polyelectrolyte multilayers (PEM) with and without adsor

211 Surfaces modified with nanometer-thick polyelectrolyte multilayers (PEMs) impregnated with silv

212 Photoreactive polyelectrolyte multilayers (PEMs) that dissolve upon UV

213 sely tuned by using layer-by-layer assembled polyelectrolyte multilayers as spacers.

214 We have employed polyelectrolyte multilayers fabricated using layer-by-la

215 ytes, hydrogen-bonding polymers, and blended polyelectrolyte multilayers have different chain packing

216 e was formed on top of microscale islands of polyelectrolyte multilayers serving as the battery elect

217 yer fabrication of biocompatible, nanoscale 'polyelectrolyte multilayers' (PEMs) on the luminal surfa

218 s, using microneedles coated with releasable polyelectrolyte multilayers.

219 y carbon electrodes, covered with an anionic polyelectrolyte Nafion, and their electrochemical proper

220 to the oppositely charged surface of a model polyelectrolyte, namely, DNA, was characterized by condu

221 ach for the in situ synthesis of metal oxide-polyelectrolyte nanocomposites formed via impregnation o

222 Synthesis of surfactant-polyelectrolyte nanoparticles was carried out in a micro

223 gly on the nature of the solute (small ions, polyelectrolyte, nanoparticles).

224 step-by-step adsorption of various species (polyelectrolytes, nanoparticles, proteins) when the laye

225 arides behave as polyelectrolytes, and their polyelectrolyte nature can be used to tune their bottom-

226 The essential polyelectrolyte nature offers the metallopolymer hydroge

227 ties of two novel narrow band gap conjugated polyelectrolytes (NBGCPEs) based on a poly[2,6-(4,4-bis-

228 l treating the humic particles as an elastic polyelectrolyte network.

229 class-2 mixed-valent triazolylbiferrocenium polyelectrolyte networks (observed inter alia by TEM and

230 ticles such as polymer-grafted nanocolloids, polyelectrolyte networks, cross-linked microgels as well

231 Self-assembling polyelectrolyte non-viral vectors can achieve both steri

232 plexes (IPECs) are typically formed when two polyelectrolytes of opposite charge are mixed together i

233 d that modifying the NP surface with anionic polyelectrolytes of varying lipophilicity can regulate t

234 m a layer-by-layer self-assembly of the same polyelectrolytes on the same PDMS moulds.

235 deposition shows that the deposition of the polyelectrolyte onto the pore walls increases the net re

236 sequential deposition of alternately charged polyelectrolytes onto a colloidal template.

237 y depositing layers of chitosan and alginate polyelectrolytes onto filter paper and physically entrap

238 hitectures of n layered electrolytes E and n polyelectrolytes PE.

239 pore with its surface modified by pH-tunable polyelectrolyte (PE) brushes connecting two large reserv

240 Polyelectrolyte (PE) wrapping of colloidal nanoparticles

241 A novel polyelectrolyte (PE)-modified nanopore, comprising a sol

242 Polyelectrolytes (PEs) are widely used in applications s

243 f highly ionic nanoparticles can behave as a polyelectrolyte "phase".

244 d on paper in a "wafer"-like bilayer film of polyelectrolytes (Poly (allyl amine hydrochloride/poly(s

245 olecular characteristics that several common polyelectrolytes, poly(acrylic acid) and poly(methylacry

246 amer and a positively charged, water-soluble polyelectrolyte Polydiallyldimethylammonium chloride (PD

247 ct deposition of nanoparticles, coating with polyelectrolytes, polymer assisted assembly of nanomater

248 Polyelectrolyte-porphyrin nanoscale assemblies consistin

249 ATP) to a solution of the anionic conjugated polyelectrolyte PPECO2 and copper(II) ion (Cu2+) recover

250 ges are observed in the case of a conjugated polyelectrolyte, presumably because the lower mobility o

251 In this work, the concept of a polyelectrolyte-promoted forward osmosis-membrane distil

252 arises from improved charge screening of the polyelectrolyte rather than specific interactions with t

253 Calculations based on linear polyelectrolytes rather than base-paired NAs underpredic

254 olymer molecules and extrinsic sites-charged polyelectrolyte repeat units balanced by counterions-wit

255 fusion requires only local rearrangements of polyelectrolyte repeat units, placing far fewer kinetic

256 -lysine as negatively and positively charged polyelectrolytes, respectively.

257 urface occurs irrespective of the charges of polyelectrolytes, resulting in the experimentally verifi

258 ding strength increases as the square of the polyelectrolyte's linear charge density and in proportio

259 The voltammetric label is a hollow polyelectrolyte shell containing approx. 1.0x10(11) Au a

260 These hydrogel beads are surrounded with a polyelectrolyte shell that encloses an enzyme, its encod

261 anocapsules of low soluble anticancer drugs, polyelectrolyte shell thickness controls drug dissolutio

262 These polyelectrolytes show excellent thermal and alkaline sta

263 structures in the presence of extrafibrillar polyelectrolytes show that the outward movement of ions

264 t of solution pH on films prepared from weak polyelectrolytes shows that when both polyelectrolytes a

265 lymers and nanoparticles by mixing them with polyelectrolyte solutions is demonstrated.

266 pplied both to characterise synthetic linear polyelectrolytes solutions and to study biomedical sampl

267 n the observation that, while the conjugated polyelectrolyte specifically inhibits the ability of sin

268 dup prevents long-range lateral diffusion of polyelectrolyte star components, hinders large-scale mic

269 ic solutions through layered electrolyte and polyelectrolyte structures are relevant in a large varie

270 arly natural colorant by copigmented complex-polyelectrolyte structures.

271 g of the conformational ensemble of flexible polyelectrolytes, such as single-stranded nucleic acids

272 in the rational design of oppositely charged polyelectrolyte-surfactant formulations for consumer pro

273 hydrated particles of a hexagonally ordered polyelectrolyte-surfactant mesophase based on the electr

274 Oppositely charged polyelectrolyte-surfactant mixtures are ubiquitous in bi

275 bling the prediction of binding strengths in polyelectrolyte-surfactant mixtures based on mesoscale p

276 EIP devices based on a synthesized dendritic polyelectrolyte that enables electrophoretic transport o

277 ells and Human Embrionic Kidney cells on two polyelectrolytes that are widely used as adhesive factor

278 architectures, which are the first class of polyelectrolytes that bear a formal charge on carbon.

279 y simultaneously spraying oppositely charged polyelectrolytes that induce surface precipitation when

280 y combination of uni-univalent salt ions and polyelectrolyte, the strength of polyelectrolyte associa

281 use, when proteins competitively bind to the polyelectrolytes, the surfactants are not capable of sus

282 rs of magnitude faster than the diffusion of polyelectrolytes themselves.

283 -ions, revealing structures not predicted by polyelectrolyte theories.

284 obs) values are consistent with limiting-law polyelectrolyte theory for +4 cationic oligopeptides bin

285 positively charged, water-soluble conjugated polyelectrolyte to detect a broad range of targets inclu

286 (Wad >/= 2 J m(-2)) of complexed catecholic polyelectrolytes to all tested surfaces including plasti

287 nocrystals are assembled layer by layer with polyelectrolytes to form high-dielectric constant gate i

288 The groundbreaking use of polyelectrolytes to increase the efficiency of supramole

289 Polydiallyldimethylammonium chloride (PDDA) polyelectrolyte was complexed with a fluorosurfactant la

290 O3 K, an anionic, narrow-band-gap conjugated polyelectrolyte, was found to be doped after dialysis.

291 Films prepared from strong polyelectrolytes, weak polyelectrolytes, hydrogen-bondin

292 y mixing the solutions of oppositely charged polyelectrolytes, which were hitherto deemed "impossible

293 ssembly behavior of pH-sensitive star-shaped polyelectrolytes with both linear and exponential growth

294 On a molecular scale histone tails are polyelectrolytes with high degree of conformational diso

295 ins by pyridine affords amphiphilic triblock polyelectrolytes with neutral/charged/neutral or charged

296 The process used two polyelectrolytes with opposite electric potentials to co

297 Star polyelectrolytes with partially screened charges and hig

298 Versatile polyelectrolytes with tunable physical properties have t

299 A new zwitterionic conjugated polyelectrolyte without free counterions has been used a

300 proper postsynthesis purification method for polyelectrolyte-wrapped NPs and reveal that apparent tox