ライフサイエンスコーパス: methacrylate

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

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

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

4 rylate) and HMAEM (hexadecylmethylaminoethyl methacrylate).

5 red with reactive polymer poly(4-nitrophenyl methacrylate).

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

7 carbon was achieved by alkylation with ethyl methacrylate.

8 layer of octadecyltrichlorosilane/polymethyl methacrylate.

9 ain transfer (RAFT) polymerization of benzyl 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 a plastic microbead suspension (poly(methyl methacrylate) (5-27 mum), polyethylene (10-27 mum), and

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 hopropyl methacrylate potassium salt, benzyl methacrylate and 4-aminothiophenol were utilized to impr

21 However, with both methacrylate and crotonate, deformylation of the initial

22 ylhexyl) adipate, dibutyl adipate, hexadecyl methacrylate and Irganox(R)1076.

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

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

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

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

27 sis of the chloroform-compatible poly(methyl methacrylate) and dimethyl sulfoxide (DMSO)-compatible p

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

29 synthesized: DMAEM (dodecylmethylaminoethyl methacrylate) and HMAEM (hexadecylmethylaminoethyl metha

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

31 f p(glycerol monomethacrylate)-b-p(Alkyl-TAF-methacrylate) and p(glycerol monomethacrylate)-b-p(Benzy

32 ic PGEA (ethanolamine-aminated poly(glycidyl methacrylate)) and type IV collagen targeted peptide (Co

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

34 lystyrene, poly(vinyl chloride), poly(methyl methacrylate), and poly(ethylene terephthalate) exhibite

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

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

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

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

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

40 chiral block copolymers (BCPs*), poly(benzyl methacrylate)-b-poly(d-cyclohexylglycolide) (PBnMA-PDCG)

41 igo(ethylene glycol) propyl sodium sulfonate methacrylate)]-b-polystyrene (POEGMA-PS), achieved by sy

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

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

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

45 f monodispersed silica filler particles in a methacrylate based resin reduces local conversion and ch

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

47 Obtained 40-nm poly(methyl methacrylate)-based NP probe, encapsulating octadecyl rh

48 es were benchmarked against similarly filled methacrylate-based bisphenol A diglycidyl ether dimethac

49 ntal adhesives that are free from 2 symbolic methacrylate-based dental resins-2-bis[4-(2-hydroxy-3-me

50 The increasing use of methacrylate-based materials in tissue engineering and d

51 t and application of a reversed-phase lauryl methacrylate-based monolith, formed in 3D printed microf

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

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

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

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

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

57 Dentin-methacrylate biointerfaces with robust and stable adhesi

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

59 ol A (BPA) leaches from bisphenol A-glycidyl methacrylate (bisGMA)-based dental materials.

60 hydrophilic poly[N,N-2-(dimethylamino)-ethyl methacrylate) block (PMMA-b-PDMAEMA), was synthesized.

61 mer, consisting of a hydrophobic poly(methyl methacrylate) block and a hydrophilic poly[N,N-2-(dimeth

62 olymer variants, poly(2-(dimethylamino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (DB) and

63 ne glycol)-block-poly(2-(dimethylamino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (ODB), se

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

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

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

67 Butyl-Methyl Methacrylate (BMMA) plastic was adopted as it preserves

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

69 100 (a copolymer based on dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate

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

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

72 nt of assembled CNT arrays within polymethyl methacrylate cavities to demonstrate centimeter-scale al

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

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

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

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

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

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

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

80 r, namely neutral-red-modified poly(glycidyl methacrylate-co-methylmethacrylate-co-poly(ethyleneglyco

81 s, poly[(oligo(ethylene glycol) methyl ether methacrylate-co-oligo(ethylene glycol) propyl sodium sul

82 SS) nanomaterials within poly(2-hydroxyethyl methacrylate-co-polyethyleneglycol methacrylate) p(HEMA-

83 We developed poly(carboxybetaine-methacrylate) coated beads to isolate L1 cell adhesion m

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

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

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

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

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

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

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

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

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

93 he same cationic poly(2-(dimethylamino)ethyl methacrylate) (D) block but placed in different architec

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

95 amino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (DB) and poly(ethylene glycol)-block-poly(

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

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

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

99 tic matrices composed of electrospun dextran methacrylate (DexMA) fibers.

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

101 Dimethylaminododecyl methacrylate (DMADDM) is a well-studied and potent antib

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

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

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

105 [2-(dimethylamino)ethyl methacrylate] (DMAEMA) was homopolymerized or copolymeri

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

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

108 esolution 3-D reconstruction method based on methacrylate embedding and serial-sectioning, where 2-D

109 500 conjugates into a thin poly(hydroxyethyl methacrylate) film; and affinity binding to edible cross

110 h brought a large number of ferrocenylmethyl methacrylate (FMMA) on the electrode surface.

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

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

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

114 UV-crosslinking of synthesized methacrylate-functionalized PDMS (MA-PDMS) is complete w

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

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

117 caffold and infuse the scaffold with gelatin methacrylate (GelMA) hydrogel to obtain a 3 D fiber hydr

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

119 l vein endothelial cells (HUVECs) in gelatin methacrylate (GelMA) hydrogel.

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

121 foxide (DMSO)-compatible poly(2-hydroxyethyl methacrylate) gels and sample setup with a preparation t

122 Here, the macroporous poly(hydroxylmethyl methacrylate/glycidyl methacrylate [p(HEMA-GMA)] cryogel

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

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

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

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

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

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

129 on included composite Marlex mesh and methyl-methacrylate, Gore-Tex, or primary closure in 57%, 28%,

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

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

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

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

134 1:1 (PE); and PE plus 10% of 2-hydroxyethyl methacrylate (HEMA) and 5% of bisphenol A glycidyl dimet

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

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

137 nsfer (RAFT) polymerization of 2-hydroxethyl methacrylate (HEMA) from a surface confined, dithio-teth

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

139 phenyl]-propane (Bis-GMA) and 2-hydroxyethyl-methacrylate (HEMA)-and have equivalent/improved bonding

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

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

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

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

144 ary epithelial cells (MECs) were cultured on methacrylated hyaluronic acid hydrogels whose stiffness

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

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

147 exceptionally smooth surfaces into a gelatin methacrylate hydrogel.

148 e dispersion polymerization of 4-nitrophenyl methacrylate in the presence of magnetite nanoparticles

149 ethyl acrylate, n-butyl acrylate, and methyl methacrylate) in broad molecular weight ranges and compo

150 nyl chloride, polypropylene, and poly(methyl methacrylate) in the edible portion of five different se

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

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

153 Methyl methacrylate is effectively polymerized by 1, with activ

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

155 obic bonded phase in the series, poly(methyl methacrylate), is found to resolve the intact constituen

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

157 of spherical cavities in a solid polymethyl methacrylate medium, driven to shock states between 0.49

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

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

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

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

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

163 loped in the presence of poly(2-hydroxyethyl methacrylate-methacryloylamidoglutamic acid) [p(HEMA-MAG

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

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

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

167 1,5,6-trimethylpyrazinium-3-olate and methyl methacrylate (MMA) yielding a lactone-lactam has been st

168 the photocatalyzed polymerization of methyl methacrylate (MMA).

169 rtion polymerization catalysts toward methyl methacrylate (MMA).

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

171 cross-linkable polypeptide of 2-hydroxyethyl methacrylate modified poly(gamma-glutamic acid) (gamma-P

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

173 us emulsion polymerization of 2-methoxyethyl methacrylate (MOEMA) has been explored for the first tim

174 , the intermediate hydrolysis products, mono-methacrylates (mono-MAs), are prepared via esterases.

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

176 ntal adhesive resin was formulated by mixing methacrylate monomers and a photoinitiator system.

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

178 Both acrylate and methacrylate monomers were successfully polymerized with

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

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

181 e glycol)-block-poly(2-(dimethylamino) ethyl methacrylate) (OD) readily encapsulate pDNA to form poly

182 amino)ethyl methacrylate)-block-poly(n-butyl methacrylate) (ODB), self-assemble into micelles, which

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

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

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

186 ophobic supports (Styrene, and two Octadecyl methacrylates (OM and OMC)).

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

188 y(Ethylene glycol Dimethacrylate-co-Glycidyl methacrylate) or poly(EDMA-co-GMA) [196.0 degrees C (+/-

189 ymerization of anionic 2-(phosphonooxy)ethyl methacrylate (P) with non-ionic glycerol monomethacrylat

190 us poly(hydroxylmethyl methacrylate/glycidyl methacrylate [p(HEMA-GMA)] cryogels with large porous su

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

192 roxyethyl methacrylate-co-polyethyleneglycol methacrylate) p(HEMA-co-EGMA) was used to render complex

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

194 AEMA) and poly(n-butyl acrylate-block-methyl methacrylate) (PBA-b-PMMA).

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

196 acrylate) (PBMA), poly(2-dimethylamino)ethyl methacrylate) (PDMAEMA) and poly(n-butyl acrylate-block-

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

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

199 crylate) (POEGMA), poly(2-dimethylaminoethyl methacrylate) (PDMAEMA), poly(sulfobetaine methacrylate)

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

201 cated at the interface between poly(glycidyl methacrylate) (PGMA) polymer brushes and Si wafer surfac

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

203 Polyhydroxyethyl methacrylate (pHEMA) hydrogels were covalently coupled w

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

205 on of electrode-tethered poly(2-hydroxyethyl methacrylate) (pHEMA) brushes of well-defined thickness

206 fabricate a fluorescent poly(2-hydroxylethyl methacrylate) (pHEMA) hydrogel that was resistant to lea

207 propyl) methacrylamide)-poly(2-hydroxypropyl methacrylate) [PHPMAC-PHPMA] diblock copolymer.

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

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

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

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

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

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

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

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

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

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

220 ehaviors in toluene, chloroform, poly(methyl methacrylate) (PMMA) film, and powder state, while its a

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

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

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

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

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

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

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

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

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

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

231 cells were grown on electrospun poly(methyl methacrylate) (PMMA) scaffolds with a diameter of 0.938

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

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

234 rticles through the formation of poly(methyl methacrylate) (PMMA) triple-helices.

235 an be achieved through tuning of poly(methyl methacrylate) (PMMA) triple-helix stereocomplexes.

236 was suitably interfaced with a poly- (methyl methacrylate) (PMMA) well-containing holders resulting i

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

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

239 the EGaIn nanodroplets(13) with poly(methyl methacrylate) (PMMA), poly(n-butyl acrylate) (PBMA), pol

240 Easily accessible poly (methyl methacrylate) (PMMA), polyethylene terephthalate (polyes

241 l-1-H-benzimidazole) (TPBi), and poly(methyl methacrylate) (PMMA), without any exciplex formation, an

242 iples, namely, laser-writing and poly(methyl methacrylate) (PMMA)-assisted lithographic processes, le

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

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

245 in, a photothermally responsive poly (methyl methacrylate) (PMMA)/paper hybrid disk (PT-Disk) was dev

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

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

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

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

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

251 ushes, including poly(oligo(ethylene glycol) methacrylate) (POEGMA), poly(2-dimethylaminoethyl methac

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

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

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

255 systems, including polystyrene, poly(methyl methacrylate), poly-L-lactic acid, polycaprolactone were

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

257 cerol monomethacrylate)-poly(2-hydroxypropyl methacrylate)-poly(ethylene glycol dimethacrylate)-poly(

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

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

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

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

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

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

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

265 Multiple monomers, 3-sulphopropyl methacrylate potassium salt, benzyl methacrylate and 4-a

266 onomer (CRM), isocyanate-terminated urethane methacrylate precursor, which has covalent affinity to d

267 tics of an ATRP reaction with a model methyl methacrylate propagating radical.

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

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

270 l methacrylate) (PDMAEMA), poly(sulfobetaine methacrylate) (PSBMA), and poly(2-(methylsulfinyl)ethyl

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

272 s, poly(vinyl)ferrocene (PVF) and poly-TEMPO-methacrylate (PTMA).

273 sted two newly developed quaternary ammonium methacrylates (QAMs) against endodontic bacteria and the

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

275 duced tissue biodegradation, and bridging to methacrylate resins.

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

277 different isomers of butanol on poly(methyl methacrylate) sheets, zinc oxide thick films, and gold t

278 etch of phenyl selenocyanate) in poly(methyl methacrylate) show that the probe dynamics are highly co

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

280 ymer segment into a hydrophilic hydroxyethyl methacrylate structure.

281 se) and monomer classes including acrylates, methacrylates, styrenics and acrylamides.

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 Using 3-(trimethoxysilyl)propyl methacrylate (TPM) as the building block, the methodolog

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

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

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

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

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

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

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

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

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

295 p(glycerol monomethacrylate)-b-p(Benzyl-TAF-methacrylate) were first characterized in a mouse subcut

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

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

298 co-methylmethacrylate-co-poly(ethyleneglycol)methacrylate) with a low redox potential of -0.58 V vs.

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