ライフサイエンスコーパス: methacrylate

1 ) designs; all CTRs were made of poly(methyl methacrylate).

2 icromolding of nanostructures in poly(methyl methacrylate).

3 nd poly(butyl methacrylate), poly(tert-butyl methacrylate).

4 P14,6,6,6][NTf2]) and the polymer poly(hexyl methacrylate).

5 he assembly of polystyrene-block-poly(methyl methacrylate).

6 r plateau regions were primarily poly(methyl methacrylate).

7 ain transfer (RAFT) polymerization of benzyl methacrylate.

8 carbon was achieved by alkylation with ethyl methacrylate.

9 layer of octadecyltrichlorosilane/polymethyl methacrylate.

10 reported for semi-fluorinated acrylates and methacrylates.

11 drohydroxyalkylation of hydroxyl-substituted methacrylate 2i with diols 1b, 1f, 1j, and 1l forms alph

12 hat a wide range of monomer types, including methacrylates, acrylamides, and styrenics, can be utiliz

13 wide range of monomers including acrylates, methacrylates, acrylamides, vinyl esters, and vinyl amid

14 Michael addition of a commercially available methacrylate-acrylate precursor in aqueous solution with

15 create tight biointerfaces with hydrophobic methacrylate adhesives on wet surfaces.

16 transition temperature polymer, poly(methyl methacrylate), adsorbed on nanoparticles and a low-glass

17 derived from the simple mixing of oxidized, methacrylated alginate (OMA) and methacrylated gelatin (

18 rs including vinyl methacrylate (VMA), allyl methacrylate (AMA), 4-vinylbenzyl methacrylate (VBMA), a

19 s, including vinyl methacrylate (VMA), allyl methacrylate (AMA), and N,N-diallyl acrylamide (DAA) by

20 nomers and the photopolymerization of methyl methacrylate and made it possible to determine the order

21 ed on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate, E) to enhance vanc

22 Copolymers of hydroxyethyl methacrylate and styrene sulfonate complex with isolated

23 The tissues were subsequently embedded in methacrylate and were sectioned so that structural chang

24 the efficacious polymerization of acrylates, methacrylates and styrene (using an identical initiator,

25 sequential monomer addition for the case of methacrylates and styrene furnishing higher molecular we

26 onalized polymers with isotactic poly(methyl methacrylate) and fullerene C60 generates supramolecular

27 ly polymerizing monomers (styrene and methyl methacrylate) and initiators that were generated rapidly

28 e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl methacrylate), poly(tert-b

29 methyl methacrylate, N,N-dimethylaminoethyl methacrylate, and 2-hydroxyethyl methacrylate lead to th

30 merization of tert-butyl methacrylate, butyl methacrylate, and ethylene glycol dimethacrylate.

31 orhexidine, nano-silver, quaternary ammonium methacrylates, and protein-repellent agents were discuss

32 Cationic poly[2-(dimethylamino)ethyl methacrylate] and anionic poly(acrylic acid) stars were

33 Poly(sorbitol methacrylate) appears to enhance activity by replacing p

34 Although acrylates and methacrylates are the state-of-the-art monomers for prot

35 sensitive indicator monomer, 2-hydroxymethyl methacrylate as a comonomer, and ethylene dimethyl metha

36 ymerization using methacrylic acid or methyl methacrylate as monomer and ethylene glycol dimethacryla

37 e (PEGA480), tert-butyl acrylate, and methyl methacrylate, as well as styrene.

38 ials that are amphiphilic (e.g., poly(methyl methacrylate)-b-poly(N,N-dimethylacrylamide)) and/or mec

39 d/or mechanically diverse (e.g., poly(methyl methacrylate)-b-poly(N,N-dimethylaminoethylmethacrylate)

40 -poly(oligo(ethylene oxide) monomethyl ether methacrylate)-b-poly(n-butyl methacrylate), prepared by

41 dithiobenzoate, for the polymerization of a methacrylate backbone under red light irradiation.

42 lycol) chains were appended to the same poly(methacrylate) backbone to generate an amphiphilic polyme

43 y (PmuSL) and uses a family of photo-curable methacrylate based copolymer networks.

44 ay to ensure high resolution of photo-curing methacrylate based SMPs that requires higher exposure en

45 Model methacrylate-based adhesives were mixed with different a

46 ryos embedded in JB-4 plastic resin-a glycol methacrylate-based medium that results in excellent pres

47 acterized both the thermal polymerization of methacrylate-based monomers and the photopolymerization

48 tyrene) is combined with an enzyme-sensitive methacrylate-based polymer segment carrying carefully de

49 ative phosphate ester monomer for bonding of methacrylate-based resins to yttria-stabilized tetragona

50 Pleurotus ostreatus on epoxy activated poly(methacrylate) beads was optimized thanks to a Response S

51 These pyrene-based methacrylate binders also enhance the stability of the s

52 Dentin-methacrylate biointerfaces with robust and stable adhesi

53 er mixture consisted of bisphenol A glycidyl methacrylate (BisGMA), hexanediol dimethacrylate (HDDMA)

54 in the gel was polystyrene-block-poly(methyl methacrylate)-block-polystyrene, where the solvophobic p

55 ed or copolymerized (50mol% each) with butyl methacrylate (BMA) from a reversible addition - fragment

56 laminoethyl methacrylate (DMAEMA), and butyl methacrylate (BMA).

57 Poly(ethylene glycol) methacrylate brush layers were prepared on quartz substr

58 A series of oil-miscible poly(lauryl methacrylate) brush-grafted silica and titania NPs were

59 We show the preparation of common poly(methacrylate) brushes and demonstrate that SI-GTP is a v

60 odification strategy in which poly(propargyl methacrylate) brushes were generated via surface-initiat

61 100 (a copolymer based on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate

62 s prepared by copolymerization of tert-butyl methacrylate, butyl methacrylate, and ethylene glycol di

63 test compounds with pHEMA (poly[hydroxyethyl methacrylate]) by ultraviolet light polymerization.

64 Benzyl methacrylate (BzMA) is polymerized using a poly(lauryl m

65 a detector on an r = 8 mum bore poly(methyl methacrylate) capillary in a split effluent stream from

66 yl-1-propanesulfonic acid and 2-hydroxyethyl methacrylate carried out through a mask afforded a 600 m

67 n a surface support displaying poly(sorbitol methacrylate) chains resulted in approximately 40-fold i

68 ization for the membrane-forming poly(benzyl methacrylate) chains.

69 onoliths based on styrene/divinylbenzene and methacrylate chemistries utilizing confocal Raman spectr

70 n, poly [2-(4-methoxyphenylamino)-2-oxoethyl methacrylate-co-divinylbenzene-co-2-acrylamido-2-methyl-

71 fabricated in a fused silica using glycidyl methacrylate-co-ethylene dimethacrylate polymer.

72 capillary prepared using GMA-EDMA (glycidyl methacrylate-co-ethylene dimethacrylate) as polymeric su

73 Monolithic poly(butyl methacrylate-co-ethylene dimethacrylate) columns have be

74 erformed on a generic hydrophobic poly(butyl methacrylate-co-ethylene dimethacrylate) layer with no i

75 The 50 microm thin poly(butyl methacrylate-co-ethylene dimethacrylate) layers supporte

76 re incorporated into the poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate) monolith by sim

77 The column is prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith throug

78 se columns are prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith throug

79 C separation of peptides using a poly(lauryl methacrylate-co-ethylene dimethacrylate) monolithic colu

80 ion of our affinity substrate, poly(glycidyl methacrylate-co-ethylene dimethacrylate) porous polymer

81 Poly(butyl methacrylate-co-ethyleneglycoldimethacrylate) [poly(BuMA

82 yer of the pH responsive polymer poly(methyl methacrylate-co-methacrylic acid) (Eudragit S100(R)).

83 plating is used to shape poly(2-hydroxyethyl methacrylate-co-methacrylic acid) hydrogel into a tissue

84 e (PHB) fibers were dip-coated by polymethyl methacrylate-co-methacrylic acid, poly(MMA-co-MAA), whic

85 on and biologic effects of poly(hydroxyethyl methacrylate-co-styrene sulfonate (P(HEMA-co-SS)).

86 adhesion was reduced (in poly(2-hydroxyethyl methacrylate-coated plates), IGF1 induced intracellular

87 y notable for a hydrophobic monomer glycidyl methacrylate combined with a nonionic surfactant Triton

88 Near-IR was used to measure methacrylate conversion after photoactivation (700 mW/cm

89 enefits are derived without compromising the methacrylate conversion of the resin component.

90 On silica (-SiOH) or poly(methyl methacrylate) (-COOH) surfaces, AEX latex attachment is

91 an oligo(ethylene glycol) (OEG) methyl ether methacrylate copolymer via RAFT polymerization.

92 f the fiber surface using a methacrylic acid/methacrylate copolymer, an antibody/antigen (IgG/anti-Ig

93 st, electrodes containing a plasticizer-free methacrylate copolymer-based sensing layer on top of a c

94 of DOTA chelators attached to a poly(methyl methacrylate) core and CANF-targeting moieties attached

95 polymerization, a biocompatible poly(methyl methacrylate)-core/polyethylene glycol-shell amphiphilic

96 as conjugated to a biocompatible poly(methyl methacrylate)-core/polyethylene glycol-shell amphiphilic

97 se with a patch-like polystyrene/poly(methyl methacrylate) corona were prepared.

98 id of P22 and cross-linked poly(2-aminoethyl methacrylate) could be useful as a new high-density deli

99 eanolic acid derivatives i.e. acrylate (D1), methacrylate (D2), methyl fumarate (D3) and ethyl fumara

100 sented here is based on the copolymer methyl methacrylate-decyl methacrylate (MMA-DMA).

101 he related addition of aryl boronic acids to methacrylate derivatives.

102 zation is used to generate a calix[4]pyrrole methacrylate-derived copolymer.

103 cerol monomethacrylate)-poly(2-hydroxypropyl methacrylate) diblock copolymer vesicles can be prepared

104 ially defined sample patterns on poly(methyl methacrylate) discs.

105 al adhesives containing dimethylaminododecyl methacrylate (DMADDM) on different bacteria in controlle

106 mer of acrylamide and 2-(dimethylamino)ethyl methacrylate (DMAEM) cross-linked with N,N'-methylenebis

107 ng of dual-responsive 2-(dimethylamino)ethyl methacrylate (DMAEMA) and light-sensitive spiropyran (SP

108 propylacrylic acid (PAA), dimethylaminoethyl methacrylate (DMAEMA), and butyl methacrylate (BMA).

109 iperazine (1-ALPP) or 2-(dimethylamino)ethyl methacrylate (DMAEMA), in combination with 2-hydroxyethy

110 [2-(dimethylamino)ethyl methacrylate] (DMAEMA) was homopolymerized or copolymeri

111 l fuel cell (see picture; PMMA = poly(methyl methacrylate), E = electrode).

112 methacrylate, butyl methacrylate and methyl methacrylate, E) to enhance vancomycin encapsulation, an

113 rylate as a comonomer, and ethylene dimethyl methacrylate (EDMA) as a cross-linker.

114 omer, oligo(ethylene oxide) monomethyl ether methacrylate, efficiently producing a polymer-GFP biocon

115 radical polymerization of a mixture of butyl methacrylate, ethylene dimethacrylate, and porogens at d

116 500 conjugates into a thin poly(hydroxyethyl methacrylate) film; and affinity binding to edible cross

117 Poly(lactic acid) and poly(methyl methacrylate) films were etched using He LTP, and the re

118 d via photografting of poly(ethylene glycol) methacrylate followed by photografting of a 4-vinyl-2,2-

119 lication toward the polymerization of methyl methacrylate for the synthesis of polymers with precisel

120 scribe how to modify the HA derivatives with methacrylates for secondary covalent cross-linking and f

121 luorotelomer alcohols (FTOHs), fluorotelomer methacrylates (FTMACs), fluorotelomer acrylates (FTACs),

122 luorotelomer alcohols (FTOHs), fluorotelomer methacrylates (FTMACs), fluorotelomer acrylates (FTACs),

123 with a tripropargylammonium headgroup and a methacrylate-functionalized hydrophobic tail were cross-

124 f oxidized, methacrylated alginate (OMA) and methacrylated gelatin (GelMA) enables simultaneous creat

125 tically align carbon nanotubes (CNTs) within methacrylated gelatin (GelMA) hydrogels in a robust, sim

126 al cells (HUVECs) encapsulated in 5% gelatin methacrylate (GelMA) hydrogel.

127 ection of DNA hybridization by using gelatin methacrylate (GelMA) modified electrodes was developed.

128 which, relative to the standard poly(methyl methacrylate) glass formed on cooling at standard rates,

129 An ethylenediamine functionalized glycidyl methacrylate (GMA) based terpolymeric chelating resin wa

130 uentially with silica (Fe3O4@SiO2), glycidyl methacrylate (GMA) by surface initiated atom transfer ra

131 Glycidyl methacrylate (GMA) was examined to provide excess epoxy

132 A) statistically copolymerized with glycidyl methacrylate (GMA), resulting in p(MMA-stat-GMA), subseq

133 nanotube (MWCNT) was grafted using glycidyl methacrylate (GMA).

134 La2O3, (ii) La2O3 embedded in poly(glycidyl methacrylate (GMA)/divinylbenzene (DVB)) tip, and (iii)

135 polymer brush of poly[oligo(ethylene glycol) methacrylate] grown by surface-initiated atom transfer r

136 ymerization of an iodoperfluoroarene-bearing methacrylate halogen bond donor were identified.

137 Cl atom initiated photodegradation of methyl methacrylate has been investigated in a 1080 L quartz-gl

138 fferent types of linkages connecting the two methacrylates have been polymerized into the correspondi

139 1:1 (PE); and PE plus 10% of 2-hydroxyethyl methacrylate (HEMA) and 5% of bisphenol A glycidyl dimet

140 (DMAEMA), in combination with 2-hydroxyethyl methacrylate (HEMA) as functional monomers, at different

141 -histidine methylester (MAH), 2-Hydroxyethyl methacrylate (HEMA) as monomers and ethyleneglycol dimet

142 sult that was not observed in a hydroxyethyl methacrylate (HEMA) homopolymer or in networks formed fr

143 neat resins containing 45 wt% 2-hydroxyethyl methacrylate (HEMA).

144 l monomethacrylate (GMA) and 2-hydroxypropyl methacrylate (HPMA).

145 dispersion polymerization of 2-hydroxypropyl methacrylate (HPMA).

146 g polymerization of 3-chloro-2-hydroxypropyl methacrylate (HPMA-Cl) and followed by L-Histidine (L-Hi

147 Methacrylated hyaluronic acid (HA) hydrogels provide a b

148 simple, miniaturized paper/PMMA (poly(methyl methacrylate)) hybrid microfluidic microplate for low-co

149 er rich in primary amines, poly(2-aminoethyl methacrylate hydrochloride-co-2-hydroxyethyl methacrylat

150 RAFT dispersion polymerization of benzyl methacrylate in alcohol using weak polyelectrolyte-based

151 ons with ethylene + methylacrylate or methyl methacrylate incorporate up to 11% acrylate comonomer, w

152 d N-hydroxysuccinimide ester or 2-aminoethyl methacrylate into OEGMA-based polymers.

153 enzyme inhibitors (i.e., quaternary ammonium methacrylates) into the resin blends has been recently p

154 block-styrene-block-(N,N-dimethylamino)ethyl methacrylate) is synthesized and used as structure-direc

155 thacrylate, producing stable PFS-poly(methyl methacrylate) latex suspensions.

156 laminoethyl methacrylate, and 2-hydroxyethyl methacrylate lead to the introduction of controlled degr

157 ated in fused-silica capillaries from lauryl methacrylate (LMA) and ethylene glycol dimethacrylate (E

158 te (BzMA) is polymerized using a poly(lauryl methacrylate) macromolecular chain transfer agent (PLMA

159 ne-functionalized poly(2-(diethylamino)ethyl methacrylate) macromonomer as a reactive steric stabiliz

160 lacrylamide (DMA), 3-(trimethoxysilyl)propyl methacrylate (MAPS) and N-Acryloyloxy succinimide (NAS).

161 DTV(2+) in a poly(methyl methacrylate) matrix was fluorescent with a spectrum sim

162 expressed at the outer and inner poly(benzyl methacrylate) membrane surface, respectively.

163 ion (PP) of di(ethylene glycol) methyl ether methacrylate (MEO2MA), a thermo-responsive monomer beari

164 orescein, and theophylline in 2-hydroxyethyl methacrylate/methacrylic acid (HEMA/MAA) copolymer hydro

165 anosensor, LOV imprinted poly(2-hydroxyethyl methacrylate-methacryloylamidoaspartic acid) [p(HEMA-MAA

166 Then, CIT-imprinted poly(2-hydroxyethyl methacrylate-methacryloylamidoglutamic acid) (p(HEMA-MAG

167 of grafted poly(acrylic acid) on poly(methyl methacrylate) micro- and nanoparticles was quantified by

168 lic acid (MAA) copolymer or a control methyl methacrylate (MM) copolymer were determined by MS.

169 entative acrylic monomers, the linear methyl methacrylate (MMA) and its cyclic analog, biomass-derive

170 tion of polar vinyl monomers [such as methyl methacrylate (MMA) and N,N-dimethylacrylamide (DMAA)] in

171 As SCNP system we employed methyl methacrylate (MMA) statistically copolymerized with glyc

172 1,5,6-trimethylpyrazinium-3-olate and methyl methacrylate (MMA) yielding a lactone-lactam has been st

173 rtion polymerization catalysts toward methyl methacrylate (MMA).

174 the photocatalyzed polymerization of methyl methacrylate (MMA).

175 d on the copolymer methyl methacrylate-decyl methacrylate (MMA-DMA).

176 hene):poly(styrenesulfonate) and poly(methyl methacrylate)-modified PCBM are utilized as the hole and

177 front end seamlessly coupled to a 5 mm long methacrylate monolith which functions as a solid-phase e

178 P was prepared by copolymerisation of methyl methacrylate (monomer) and ethylene glycol dimethacrylat

179 SN (denoted as CHX@MSN) were fabricated with methacrylate monomers and silanized glass fillers (CHX o

180 Both acrylate and methacrylate monomers were successfully polymerized with

181 nsaturated groups directly into zwitterionic methacrylate monomers, specifically choline phosphate st

182 th traditional vinyl monomers such as methyl methacrylate, N,N-dimethylaminoethyl methacrylate, and 2

183 immobilized to the surface of poly(glycidyl methacrylate) nanoparticles (PGMA NPs).

184 virus (HSV) assay where oligoethylene glycol methacrylate (OEGMA) grafted ssDNA capture-probes on par

185 hydrogels based upon oligo(ethylene glycol) methacrylate (OEGMA) monomers has been previously report

186 ATRP of oligo(ethylene glycol) methyl ether methacrylate (OEGMA) yielded a site-specific (C-terminal

187 zation of oligo(ethylene oxide) methyl ether methacrylate (OEOMA) in the presence of CuBr2 catalyst a

188 d on octadecyl methacylate (OM) or octadecyl methacrylate (OMC) beads.

189 yl-1-propanesulfonic acid and 2-hydroxyethyl methacrylate on top of the generic hydrophobic monolith

190 mples, an interface with poly(2-hydroxyethyl methacrylate) p(HEMA) brush was employed.

191 still leading to highly isotactic poly(allyl methacrylate) (PAMA) with 95-97% [mm].

192 poly(butadiene-block-2-(dimethylamino)ethyl methacrylate) (PB-b-PDMAEMA) diblock copolymers as struc

193 lic acid) (PAA), poly(5-cholesteryloxypentyl methacrylate) (PC5MA), and poly(ethylene oxide) (PEO) bl

194 Poly(cysteine methacrylate) (PCysMA) brushes were grown from the surfa

195 pH responsive poly(N,N-(dimethylamino)ethyl methacrylate) (PDMAEMA) and their copolymers were analyz

196 hes derived from poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) in water vapor is investigated u

197 matrix composed of poly(ethylene-co-glycidyl methacrylate) (PEGM) has been prepared.

198 r, poly(ethylene oxide)-block-poly(octadecyl methacrylate) (PEO(39)-b-PODMA(17)), in aqueous dispersi

199 elles with a LC poly(2-(perfluorooctyl)ethyl methacrylate (PFMA) core via a fragmentation-thermal ann

200 cerol monomethacrylate)-poly(2-hydroxypropyl methacrylate) (PGMA-PHPMA) diblock copolymer vesicles we

201 Polyhydroxyethyl methacrylate (pHEMA) hydrogels were covalently coupled w

202 shes: hydroxy-functional poly(2-hydroxyethyl methacrylate) (pHEMA) and carboxy-functional poly(carbox

203 gers localized growth of poly(hydroxyl-ethyl methacrylate) (PHEMA) brush, contributing to marked SPR

204 olic) acid (PLGA) films in poly(hydroxyethyl methacrylate) (pHEMA) by ultraviolet photopolymerization

205 A poly(2-hydroxyethyl-methacrylate) (pHEMA) hydrogel was developed to achieve

206 th of polymer brushes of poly(hydroxyl-ethyl methacrylate) (PHEMA) via an ATRP mechanism.

207 a short middle block of poly(2-hydroxyethyl methacrylates) (PHEMA) that is randomly functionalized b

208 from their growth substrate using polymethyl methacrylate (PMMA) and a wet etch to allow the user to

209 ured polymers (polystyrene (PS)-b-polymethyl methacrylate (PMMA) block copolymers (BCP)) using either

210 P sensing cartridge integrating a polymethyl methacrylate (PMMA) micro-reactor with a polycarbonate (

211 on beam lithography at 100 kV and polymethyl methacrylate (PMMA) resist at different thicknesses.

212 matrix made by laser engraving of polymethyl methacrylate (PMMA) sheet as off surface matrix was inte

213 esis (KPro) biointegration, using polymethyl methacrylate (PMMA)--the principal component of the Bost

214 Poly-methyl methacrylate (PMMA)-based dental resins with strong and

215 ials calcium sulfate (CaSO4) and poly methyl methacrylate (PMMA).

216 Ultrathin poly(methyl methacrylate) PMMA films were prepared on gold substrate

217 nate (TPGS), Polysorbate 80, and poly(methyl methacrylate) (PMMA) as analytes.

218 selectivity and sensitivity of a poly(methyl methacrylate) (PMMA) based QCM sensor can be significant

219 id (PAA) block and a hydrophobic poly(methyl methacrylate) (PMMA) block was developed to similarly re

220 erated polystyrene (d(8)-PS) and poly(methyl methacrylate) (PMMA) blocks, as well as a short middle b

221 poles in commonly used spherical poly(methyl methacrylate) (PMMA) colloids, suspended in an apolar or

222 , "nacre-mimetic" hydroxyapatite/poly(methyl methacrylate) (PMMA) composites are developed by process

223 We describe a poly(methyl methacrylate) (PMMA) dip-coating procedure, which result

224 ing modes associated with a thin poly(methyl methacrylate) (PMMA) film that is coupled to a silver-co

225 d without using the conventional poly(methyl methacrylate) (PMMA) for graphene transfer from a growth

226 e of CO2 laser micromachining on poly(methyl methacrylate) (PMMA) has the potential for flexible, low

227 velengths (450-470 nm) both in a poly(methyl methacrylate) (PMMA) matrix and in solution at 77 K.

228 The poly(methyl methacrylate) (PMMA) microchips feature integral in-plan

229 were surface chemistries within poly(methyl methacrylate) (PMMA) microfluidic channels that enabled

230 albumin (BSA), respectively, on poly(methyl methacrylate) (PMMA) micropillar surfaces, as well as as

231 ipulate conductive silver-coated Poly(methyl methacrylate) (PMMA) microspheres (50 mum diameter) into

232 paration of polystyrene (PS) and poly(methyl methacrylate) (PMMA) microspheres based entirely on thei

233 genase (apo-GDH), is loaded into poly(methyl methacrylate) (PMMA) nanospheres in the presence of meth

234 Poly(methyl methacrylate) (PMMA) optical fibers in a series of diffe

235 The system utilizes a poly(methyl methacrylate) (PMMA) or glass substrates sputtered by 40

236 As poly (methyl methacrylate) (PMMA) remains the main material employed

237 be stabilised by using a porous poly(methyl methacrylate) (PMMA) sacrificial layer, which creates a

238 s of electromagnetically coupled poly(methyl methacrylate) (PMMA) spheres with wavelength-scale diame

239 by smaller (approximately 3 mm) poly(methyl methacrylate) (PMMA) spherical beads, threaded on a flex

240 d by a microchannel assembled in poly(methyl methacrylate) (PMMA) substrate connected to an amperomet

241 notubes are press-transferred on poly(methyl methacrylate) (PMMA) substrates and are easily coupled t

242 The VG system exploited poly(methyl methacrylate) (PMMA) substrates of high optical quality

243 y bionanocomposite directly on a poly(methyl methacrylate) (PMMA) surface (also known as plexiglass o

244 been used for the separation of poly(methyl methacrylate) (PMMA) with regard to molecular microstruc

245 Four different polymers, poly(methyl methacrylate) (PMMA), poly(ethylene terephthalate) (PET)

246 operties from the thermoplastics poly(methyl methacrylate) (PMMA), polystyrene (PS), polycarbonate (P

247 hography at sites of interest on poly(methyl methacrylate) (PMMA)-covered monolayer MoS2 triangles.

248 trations polystyrene (PS) and poly(methylene methacrylate) (PMMA).

249 als such as polystyrene (PS) and poly(methyl methacrylate) (PMMA).

250 or the first time, stereoregular poly(methyl methacrylates) (PMMAs) were separated according to tacti

251 horylcholine-block-2-(diisopropylamino)ethyl methacrylate) [PMPC-PDPA]: the biomimetic PMPC block is

252 rylcholine]-block-[2-(diisopropylamino)ethyl methacrylate] (PMPC-PDPA), a pH-sensitive diblock copoly

253 which consist of poly(oligo(ethylene glycol) methacrylate) (POEG) hydrophilic blocks and dasatinib (D

254 anoparticles into poly(oligo(ethylene glycol)methacrylate) (POEGMA) brushes grown on glass.

255 d cross-linking of poly(oligoethylene glycol methacrylate) (POEGMA) derivatives that reduces nonspeci

256 methacrylate hydrochloride-co-2-hydroxyethyl methacrylate) (poly(AMA-co-HEMA)) was first grafted from

257 A pH-responsive poly(2-dimethylaminoethyl methacrylate) [poly(DMAEMA)] hydrogel is synthesized and

258 er, poly(oligo(ethylene glycol) methyl ether methacrylate) [poly(OEGMA)], with low polydispersity and

259 e, poly(methyl methacrylate), and poly(butyl methacrylate), poly(tert-butyl methacrylate).

260 first time that poly(ammonium 2-sulfatoethyl methacrylate)-poly(benzyl methacrylate) [PSEM-PBzMA] dib

261 ess and transforms the initially hydrophobic methacrylate polymer segment into a hydrophilic hydroxye

262 separated poly(2-vinylpyridine)/poly(methyl methacrylate) polymer thin film.

263 Porphyrin-doped hybrid PMMA [poly(methyl methacrylate)] polymer films demonstrate the reversibili

264 A class of methacrylate polymers based on a polycyclic aromatic hyd

265 t the synthesis of novel azulene-substituted methacrylate polymers by free radical polymerization, in

266 poly(methacrylic acid)-g-poly(ethyleneglycol methacrylate) polymers as in situ coating agents for mag

267 d in azobenzene-based syndiotactic-rich poly(methacrylate) polymers.

268 oly(ethylene glycol)s (mPEGs) and poly(mPEG) methacrylate prepared by atom transfer radical polymeriz

269 onomethyl ether methacrylate)-b-poly(n-butyl methacrylate), prepared by atom-transfer radical polymer

270 n the microemulsion polymerization of methyl methacrylate, producing stable PFS-poly(methyl methacryl

271 Copolymers of azulene with zwitterionic methacrylates proved useful as cathode modification laye

272 We demonstrate the use of poly(sulfobetaine methacrylate) (PSBMA), and its pyrene-containing copolym

273 ium 2-sulfatoethyl methacrylate)-poly(benzyl methacrylate) [PSEM-PBzMA] diblock copolymer nanoparticl

274 4-styrenesulfonate-co-poly(ethylene glycol) methacrylate) (pSS-co-pPEGMA) was synthesized by reversi

275 surface immobilized poly(triethylene glycol methacrylate) (pTEGMA) that exhibits significant thermal

276 lic peptide ligand was synthesized on a poly(methacrylate) resin and used for chromatographic binding

277 duced tissue biodegradation, and bridging to methacrylate resins.

278 In addition, chain extensions of poly(methacrylate)s, poly(styrene), poly(N-vinyl pyrrolidinon

279 styrene-block-polyethylene-block-poly(methyl methacrylate) (SEM), well-defined worm-like CCMs with a

280 nyl chloride) backbones and poly(oxyethylene methacrylate) side chains, i.e., PVC-g-POEM as templates

281 ymer segment into a hydrophilic hydroxyethyl methacrylate structure.

282 A tripropargylammonium surfactant with a methacrylate-terminated hydrophobic tail was combined wi

283 id was chemically modified with hydroxyethyl methacrylate to form hydrolytically degradable hydrogels

284 other resins containing quaternary ammonium methacrylates to suppress plaque buildup and bacterial a

285 radius silica and 9.8 mum radius poly(methyl methacrylate) tubes and automated time/pressure based hy

286 applied to concrete are simulated, namely a methacrylate type PCE (PCEM-P), an allyl ether type PCE

287 isting of styrene sulfonate units and methyl methacrylate units bearing poly(ethylene glycol) side ch

288 in PMMA/Viton/PMMA [where PMMA = poly(methyl methacrylate)], utilizes on-chip valving, and is scalabl

289 MA), allyl methacrylate (AMA), 4-vinylbenzyl methacrylate (VBMA), and N,N-diallyl acrylamide (DAA).

290 onyloxy)anthracene-1,9-dicarboxyimide-methyl methacrylate (VBSADI-MMA) and N-(p-vinylbenzenesulfonylo

291 y and were further copolymerized with lauryl methacrylate via a simple one-step free radical polymeri

292 on of polar divinyl monomers including vinyl methacrylate (VMA), allyl methacrylate (AMA), 4-vinylben

293 tive polar divinyl monomers, including vinyl methacrylate (VMA), allyl methacrylate (AMA), and N,N-di

294 sfer radical polymerization (ATRP) of methyl methacrylate was investigated using several phenothiazin

295 ntum dots into photo-polymerized poly(lauryl methacrylate), we obtain freestanding, colourless slabs

296 hydrogel of the polymer poly(2-hydroxyethyl methacrylate), which is then recovered using centrifugat

297 nched selectivity is even achieved for ethyl methacrylate, which enables the introduction of a quater

298 methacrylate monomer or bisphenol A glycidyl methacrylate, which is a monomer standard in dental mate

299 opolymers based on poly(styrene-block-methyl methacrylate) with various molecular weights and composi

300 rol monomethacrylate)55-poly(2-hydroxypropyl methacrylate)x (G55-Hx) vesicles prepared by polymerizat