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1

Kim, Dong-Hyun, Tae-Hun Kim, and A.-Young Sung. "Ophthalmic Application of Polymer with High Oxygen Transmissibility Containing 2-(trimethylsilyloxy)ethyl Methacrylate." Journal of the Korean Chemical Society 57, no. 3 (2013): 405–10. http://dx.doi.org/10.5012/jkcs.2013.57.3.405.

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2

Ritz, Pavel, Petra Látalová, Jaroslav Kříž, Jan Genzer, and Petr Vlček. "Statistical copolymers of 2-(trimethylsilyloxy)ethyl methacrylate and methyl methacrylate synthesized by ATRP." Journal of Polymer Science Part A: Polymer Chemistry 46, no. 5 (2008): 1919–23. http://dx.doi.org/10.1002/pola.22436.

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3

Yoshida, Hidekazu, Shinichi Itsuno, and Koichi Ito. "Syntheses and interfacial characterization of graft copolymers from styrene and 2-hydroxyethyl methacrylate that comprise either trunks or branches." Canadian Journal of Chemistry 73, no. 11 (1995): 1757–64. http://dx.doi.org/10.1139/v95-216.

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Polystyrene (PS) and poly(2-hydroxyethyl methacrylate) (PHEMA) macromonomers with either p-vinylbenzyl or methacrylate end groups were prepared by living anionic polymerizations of styrene and 2-(trimethylsilyloxy)ethyl methacrylate, respectively, followed by appropriate end-capping. They were radically copolymerized with 2-hydroxyethyl methacrylate and styrene, respectively, to afford PS-g-PHEMA and PHEMA-g-PS, having PS trunks with PHEMA branches or the reverse architecture. 1H NMR spectra of the graft copolymers in deuterated methanol showed their micelle formation with PS and PHEMA chains
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4

Lee, Bong-Seop, Jae-Kyung Lee, Jae-Hwi Bong, and Hun-Soo Byun. "Phase behavior for the 2-(trimethylsilyloxy)ethyl methacrylate and 3-(trimethoxysilyl)propyl methacrylate in supercritical carbon dioxide." Fluid Phase Equilibria 462 (April 2018): 1–5. http://dx.doi.org/10.1016/j.fluid.2018.01.013.

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5

Kim, So Yeun, Jae-Hyung Wee, Cheol-Min Yang, and Bo-Hye Kim. "Electrochemical capacitor performance of 2-(trimethylsilyloxy)ethyl methacrylate-derived highly mesoporous carbon nanofiber composite containing MnO 2." Journal of Electroanalytical Chemistry 801 (September 2017): 403–9. http://dx.doi.org/10.1016/j.jelechem.2017.07.028.

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6

Osicka, Josef, Miroslav Mrlik, Markéta Ilčíková, et al. "Light-Induced Actuation of Poly(dimethylsiloxane) Filled with Graphene Oxide Grafted with Poly(2-(trimethylsilyloxy)ethyl Methacrylate)." Polymers 10, no. 10 (2018): 1059. http://dx.doi.org/10.3390/polym10101059.

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This study serves to combine two approaches into one single step, to achieve a significant improvement of the light-induced actuation capabilities. Graphene oxide (GO) is an inert material, from the electrical and thermal conductivity point of view, and is incompatible with the usually-used poly(dimethylsiloxane) (PDMS) matrix. During surface-modification by surface-initiated atom transfer radical polymerization, the GO was transformed into a conducting and compatible material with the PDMS showing enormous light-induced actuation capability. The GO surface-modification with poly(2-(trimethyls
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7

Kutalkova, Erika, Miroslav Mrlik, Marketa Ilcikova, Josef Osicka, Michal Sedlacik, and Jaroslav Mosnacek. "Enhanced and Tunable Electrorheological Capability using Surface Initiated Atom Transfer Radical Polymerization Modification with Simultaneous Reduction of the Graphene Oxide by Silyl-Based Polymer Grafting." Nanomaterials 9, no. 2 (2019): 308. http://dx.doi.org/10.3390/nano9020308.

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In this study, a verified process of the "grafting from" approach using surface initiated atom transfer radical polymerization was applied for the modification of a graphene oxide (GO) surface. This approach provides simultaneous grafting of poly(2-(trimethylsilyloxy)ethyl methacrylate) (PHEMATMS) chains and a controllable reduction of the GO surface. This allows the fine tuning of its electrical conductivity, which is a crucial parameter for applications of such hybrid composite particles in electrorheological (ER) suspensions. The successful coating was confirmed by transmission electron mic
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8

Aly, A. A., H. M. Ammar, and A. A. Khalil. "Copolymerization Parameters of 2-(N-Phthalimido) ethyl Methacrylate with Different Vinyl Monomers." Material Science Research India 8, no. 1 (2011): 17–24. http://dx.doi.org/10.13005/msri/080103.

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2-(N-phthalimido)ethyl methacrylate was prepared by the reaction of methacrylic acid with N-(2-hydroxyethyl)phthalimide in presence of N,N?-dicyclohexylcarbodiimide. The monomer reactivity ratios for copolymerization reactions of 2-(N-phthalimido)ethyl methacrylate with methyl acrylate, ethyl acrylate, butyl acrylate and styrene, respectively, in solution with azobisisobutyronitrile (AIBN) as initiator, were estimated by nitrogen analysis. The structure of the copolymers was investigated by IR spectroscopy. The Q and e values for 2-(N-phthalimido)ethyl methacrylate were calculated. Some of the
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9

Schneider, Bohdan, Jan Štokr, Jaroslav Straka, Martin Přádný, and Stanislav Ševčík. "Conformational structure of poly[2-(dimethylamino)ethyl methacrylate], 2-(dimethylamino)ethyl pivalate and of their quaternary iodides. Vibrational and NMR spectra." Collection of Czechoslovak Chemical Communications 53, no. 12 (1988): 3097–107. http://dx.doi.org/10.1135/cccc19883097.

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Raman, infrared, and 1H and 13C NMR spectra of 2-(dimethylamino)ethyl pivalate, 2-(pivaloyloxy)ethyltrimethylammonium iodide, poly[2-(dimethylamino)ethyl methacrylate] and of its quaternary iodide were measured. Spectral analysis revealed that in crystalline 2-(dimethylamino)ethyl pivalate and in its quaternary salt, the 2-(dimethylamino)ethyl group exists in the g conformational state. In the liquid state, these compounds also contain a smaller amount of the t conformational structure of the 2-(dimethylamino)ethyl group. In poly[2-(dimethylamino)ethyl methacrylate] and in its quaternary iodid
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10

Pei, Yiwen, Nadia C. Dharsana, and Andrew B. Lowe. "Ethanolic RAFT Dispersion Polymerization of 2-(Naphthalen-2-yloxy)ethyl Methacrylate and 2-Phenoxyethyl Methacrylate with Poly[2-(dimethylamino)ethyl Methacrylate] Macro-Chain Transfer Agents." Australian Journal of Chemistry 68, no. 6 (2015): 939. http://dx.doi.org/10.1071/ch14490.

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The ethanolic reversible addition-fragmentation chain transfer dispersion polymerization (RAFTDP), at 21 wt-%, of 2-(naphthalen-2-yloxy)ethyl methacrylate (NOEMA) and 2-phenoxyethyl methacrylate (POEMA) with a poly[2-(dimethylamino)ethyl methacrylate] macro-chain transfer agent (CTA) with an average degree of polymerization of 20 (PDMAEMA20) is described. DMAEMA20-b-NOEMAy (y = 20–125) block copolymers were readily prepared under dispersion conditions in ethanol at 70°C. However, the polymerization of NOEMA was not well controlled, with size exclusion chromatograms being distinctly bi or multi
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11

Guan, Jian, Xiaodi Yu, Minghui He, et al. "Synthesis of Ultrahigh Molecular Weight Poly (Trifluoroethyl Methacrylate) Initiated by the Combination of Palladium Nanoparticles with Organic Halides." Polymers 16, no. 19 (2024): 2764. http://dx.doi.org/10.3390/polym16192764.

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Ultrahigh molecular weight polymers display outstanding properties and have great application potential. However, the traditional polymerization methods have inevitable disadvantages that challenge the green synthesis of ultrahigh molecular weight polymers. The paper achieved an ultrahigh molecular weight poly (trifluoroethyl methacrylate) via a novel polymerization and discussed the mechanistic, kinetic, and experimental aspects. The combination of palladium nanoparticles with ethyl 2-bromopropionate has been identified as an exceedingly efficient system for initiating the polymerization of t
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12

Miranda, Larissa N., and Warren T. Ford. "Binary copolymer reactivity oftert-butyl methacrylate, 2-(N,N-dimethylamino)ethyl methacrylate, solketal methacrylate, and 2-bromoethyl methacrylate." Journal of Polymer Science Part A: Polymer Chemistry 43, no. 19 (2005): 4666–69. http://dx.doi.org/10.1002/pola.20939.

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13

Schlaad, Helmut, Theodora Krasia, and Markus Antonietti. "Superhelices of Poly[2-(acetoacetoxy)ethyl methacrylate]." Journal of the American Chemical Society 126, no. 36 (2004): 11307–10. http://dx.doi.org/10.1021/ja047858z.

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14

Topaloğlu Yazıcı, D., A. Aşkın, and V. Bütün. "Surface characteristics of 2-(diethylamino) ethyl methacrylate–2-(dimethylamino) ethyl methacrylate diblock copolymer determined by inverse gas chromatography." Surface and Interface Analysis 38, no. 4 (2006): 561–64. http://dx.doi.org/10.1002/sia.2226.

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15

Aluani, Denitsa, Magdalena Kondeva-Burdina, Alexandra Tosheva, Krassimira Yoncheva, and Virginia Tzankova. "Improvement of in vitro antioxidant activity of kaempferol by encapsulation in copolymer micelles." Pharmacia 69, no. (1) (2022): 25–29. https://doi.org/10.3897/pharmacia.69.e77678.

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Antioxidant capacity of poorly soluble natural antioxidant kaempferol, in particular free or loaded in two types of cationic micelles, was studied on non-enzyme induced lipid peroxidation (LPO) in vitro. The micelles were based on triblock copolymers - poly(2-(dimethylamino)ethyl methacrylate-b-poly(propylene oxide)-b-poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA-PPO-PDMAEMA) and poly(2-(dimethylamino)ethyl methacrylate-b-poly(ε-caprolactone)-b-poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA-PCL-PDMAEMA). The lipid peroxidation was induced by incubating of rat liver microsomes with iron
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16

You, Qian Qian, and Pu Yu Zhang. "Synthesis of Copper Complexes of Poly [2-(dimethylamino ethyl methacrylate)-B-Poly (oligo (ethylene glycol) monomethylether methacrylate-B-Poly [2-(dimethylamino ethyl methacrylate)." Advanced Materials Research 668 (March 2013): 145–48. http://dx.doi.org/10.4028/www.scientific.net/amr.668.145.

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Three different ratios of double hydrophilic block copolymers poly [2-(dimethylamino) ethyl methacrylate]-b-poly(oligo(ethylene oxide) monomethyl ether methacrylate)-b-poly [2-(dimethylamino) ethyl methacrylate] (PDMAEMA-b-POEOMA-b-PDMAEMA) were synthesized by reversible addition fragmentation chain-transfer polymerization (RAFT), which was one of the controlled/living radical polymerization. The chain structure and component of such copolymers were characterized by spectroscopic studies (FTIR, 1H NMR). The interaction of PDMAEMA-b-POEOMA-b-PDMAEMA copolymers with copper sulfate and copper chl
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17

Aluani, Denitsa, Magdalena Kondeva-Burdina, Alexandra Tosheva, Krassimira Yoncheva, and Virginia Tzankova. "Improvement of in vitro antioxidant activity of kaempferol by encapsulation in copolymer micelles." Pharmacia 69, no. 1 (2022): 25–29. http://dx.doi.org/10.3897/pharmacia.69.e77678.

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Antioxidant capacity of poorly soluble natural antioxidant kaempferol, in particular free or loaded in two types of cationic micelles, was studied on non-enzyme induced lipid peroxidation (LPO) in vitro. The micelles were based on triblock copolymers - poly(2-(dimethylamino)ethyl methacrylate-b-poly(propylene oxide)-b-poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA-PPO-PDMAEMA) and poly(2-(dimethylamino)ethyl methacrylate-b-poly(ε-caprolactone)-b-poly(2-(dimethylamino)ethyl methacrylate (PDMAEMA-PCL-PDMAEMA). The lipid peroxidation was induced by incubating of rat liver microsomes with iron
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18

Shatan, Anastasiia B., Vitalii Patsula, Aneta Dydowiczová, et al. "Cationic Polymer-Coated Magnetic Nanoparticles with Antibacterial Properties: Synthesis and In Vitro Characterization." Antibiotics 10, no. 9 (2021): 1077. http://dx.doi.org/10.3390/antibiotics10091077.

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Uniformly sized magnetite nanoparticles (Dn = 16 nm) were prepared by a thermal decomposition of Fe(III) oleate in octadec-1-ene and stabilized by oleic acid. The particles were coated with Sipomer PAM-200 containing both phosphate and methacrylic groups available for the attachment to the iron oxide and at the same time enabling (co)polymerization of 2-(dimethylamino)ethyl methacrylate and/or 2-tert-butylaminoethyl methacrylate at two molar ratios. The poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) and poly[2-(dimethylamino)ethyl methacrylate-co-2-tert-butylaminoethyl methacrylate] [P(DM
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19

Taktak, Fulya, Murat Yildiz, Hakan Sert, and Cengiz Soykan. "A Novel Triple-Responsive Hydrogels Based on 2-(Dimethylamino) Ethyl Methacrylate by Copolymerization With 2-(N-morpholino) Ethyl Methacrylate." Journal of Macromolecular Science, Part A 52, no. 1 (2014): 39–46. http://dx.doi.org/10.1080/10601325.2014.976747.

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20

Saricilar, Sureyya, Robert Knott, Christopher Barner-Kowollik, Thomas P. Davis, and Johan P. A. Heuts. "Reversible addition fragmentation chain transfer polymerization of 3-[tris(trimethylsilyloxy) silyl] propyl methacrylate." Polymer 44, no. 18 (2003): 5169–76. http://dx.doi.org/10.1016/s0032-3861(03)00520-2.

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21

Balci, Nurcan, Ural Akbulut, Levent Toppare, Dietmar Stanke, and Manfred L. Hallensleben. "Polypyrrole grafts with poly[(methyl methacrylate)-co-(2-(N-pyrrolyl) ethyl methacrylate)]." Materials Research Bulletin 32, no. 10 (1997): 1449–58. http://dx.doi.org/10.1016/s0025-5408(97)00124-4.

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22

Reiter, Jakub, Jiří Michálek, Jiří Vondrák, Dana Chmelíková, Martin Přádný, and Zdeněk Mička. "Poly(ethyl methacrylate) and poly(2-ethoxyethyl methacrylate) based polymer gel electrolytes." Journal of Power Sources 158, no. 1 (2006): 509–17. http://dx.doi.org/10.1016/j.jpowsour.2005.07.075.

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23

Jayakumar, R., R. Balaji, and S. Nanjundan. "Studies on copolymers of 2-(N-phthalimido)ethyl methacrylate with methyl methacrylate." European Polymer Journal 36, no. 8 (2000): 1659–66. http://dx.doi.org/10.1016/s0014-3057(99)00244-x.

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24

Cho, Young-Sun, Jae-Suk Lee, and Gyoujin Cho. "Anionic polymerization of 2-( N -carbazolyl)ethyl methacrylate." Polymer 43, no. 4 (2002): 1197–202. http://dx.doi.org/10.1016/s0032-3861(01)00728-5.

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25

Barral, Silvia, António Guerreiro, María A. Villa-García, Manuel Rendueles, Mario Díaz, and Sergey Piletsky. "Synthesis of 2-(diethylamino)ethyl methacrylate-based polymers." Reactive and Functional Polymers 70, no. 11 (2010): 890–99. http://dx.doi.org/10.1016/j.reactfunctpolym.2010.08.003.

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26

Ni, Pei-Hong, Qi-Sheng Pan, Liu-Sheng Zha, Chang-Chun Wang, Abdelhamid Elaïssari, and Shou-Kuan Fu. "Syntheses and characterizations of poly[2-(dimethylamino)ethyl methacrylate]-poly(propylene oxide)-poly[2-(dimethylamino)ethyl methacrylate] ABA triblock copolymers." Journal of Polymer Science Part A: Polymer Chemistry 40, no. 4 (2002): 624–31. http://dx.doi.org/10.1002/pola.10144.

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27

Bradley, Melanie, Brian Vincent, and Gary Burnett. "Biocompatible, Polyampholyte Microgel Particles." Australian Journal of Chemistry 60, no. 9 (2007): 646. http://dx.doi.org/10.1071/ch07098.

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Biocompatible, polyampholyte microgel particles have been prepared by the acid hydrolysis of t-butyl groups within (2-diethylamino)ethyl methacrylate-co-t-butyl methacrylate microgel particles to give (2-diethylamino)ethyl methacrylate-co-methacrylic acid microgel particles. The hydrodynamic diameter and electrophoretic mobility of both the pre-hydrolyzed and post-hydrolyzed microgel particles have been investigated as a function of pH for three microgel dispersions differing in their monomer compositions. The swelling properties and isoelectric point pH are shown to depend on the monomer comp
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28

Huo, Meng, Min Zeng, Decheng Wu, Yen Wei, and Jinying Yuan. "Topological engineering of amphiphilic copolymers via RAFT dispersion copolymerization of benzyl methacrylate and 2-(perfluorooctyl)ethyl methacrylate for polymeric assemblies with tunable nanostructures." Polymer Chemistry 9, no. 7 (2018): 912–19. http://dx.doi.org/10.1039/c8py00029h.

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29

Lee, Taeheon, Jaehyun Park, Kyoungho Kim, et al. "Facile tuning of a polymeric dispersant for single-walled carbon nanotube dispersion." RSC Advances 5, no. 85 (2015): 69410–17. http://dx.doi.org/10.1039/c5ra10350a.

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30

Benjamin, C. C., R. J. Craven, W. C. Crone, and R. S. Lakes. "Viscoelastic characterization of pH-sensitive 2-hydroxyethyl methacrylate (2-dimethylamino) ethyl methacrylate HEMA-DMAEMA hydrogels." Polymer Testing 72 (December 2018): 372–76. http://dx.doi.org/10.1016/j.polymertesting.2018.10.045.

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31

Pei, Yiwen, and Andrew B. Lowe. "Polymerization-induced self-assembly: ethanolic RAFT dispersion polymerization of 2-phenylethyl methacrylate." Polym. Chem. 5, no. 7 (2014): 2342–51. http://dx.doi.org/10.1039/c3py01719b.

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Reversible addition-fragmentation chain transfer (RAFT) radical dispersion polymerization (RAFTDP) has been employed to polymerize 2-phenylethyl methacrylate (PEMA) using poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) macromolecular chain transfer agents (macro-CTAs) of varying average degree of polymerization (X̄<sub>n</sub>).
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32

He, Wei, and Xiao Nan Huang. "pH-Sensitive Materials with Controllable pH Phase Transition Value." Applied Mechanics and Materials 727-728 (January 2015): 219–22. http://dx.doi.org/10.4028/www.scientific.net/amm.727-728.219.

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Novel pHsensitive methacrylate-based (co)polymers with pendent tertiary amine groups were prepared by free radical polymerization of monomer 2-(dimethylamino)ethyl methacrylate (DMA) and 2-(Dibutylamino)ethyl methacrylate (DBA). These polymers are pH sensitive in aqueous solution, which was studied by titration, transmittance measurements experiment. The pH responsive polymers dissociate at lower pH value because of the electrostatic repulsion and aggregate above their pH responsive value induced by hydrophobic interaction of pendent group. The pH responsive value of (co)polymers can be contro
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33

Raj, Wojciech, Alessandro Russo, Yaoming Zhang, Julien Chapelat, and Joanna Pietrasik. "Renewable Fabric Surface-Initiated ATRP Polymerizations: Towards Mixed Polymer Brushes." Nanomaterials 10, no. 3 (2020): 536. http://dx.doi.org/10.3390/nano10030536.

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A totally new approach in the synthesis of mixed polymer brushes tethered on polyamide (PA) surfaces is presented herein. As a proof of concept, two types of homopolymers were synthesized in sequential surface-initiated atom transfer radical polymerization (SI-ATRP) reactions: poly(methyl methacrylate)/poly((2-dimethylamino)ethyl methacrylate) and polystyrene /poly((2-dimethylamino)ethyl methacrylate). The ATRP initiator was immobilized on the surface through PA chain-end groups in two subsequent steps, separated by homo-polymerizations. The amount of the PA chains’ end groups available on the
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34

Knezevic, Marija, Lynne Katsikas, and Ivanka Popovic. "The synthesis and characterization of 2-mercaptoethyl methacrylate." Chemical Industry 59, no. 11-12 (2005): 321–23. http://dx.doi.org/10.2298/hemind0512321k.

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The synthesis of 2-mercaptoethyl methacrylate from methacrylic acid and 2-mercaptoethanol by etherification using acetyl chloride as catalyst was optimized. The purity of the obtained product was controlled by gas chromatography and its identity confirmed by H-NMR and FTIR spectroscopy. 2-Mercapto-ethyl methacrylate could find application as a chain transfer agent in radical polymerizations.
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35

Liechty, William B., Rebekah L. Scheuerle, and Nicholas A. Peppas. "Tunable, responsive nanogels containing t-butyl methacrylate and 2-(t-butylamino)ethyl methacrylate." Polymer 54, no. 15 (2013): 3784–95. http://dx.doi.org/10.1016/j.polymer.2013.05.045.

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36

Sigel, Reinhard, Theodora Krasia-Christoforou, Ines Below, and Helmut Schlaad. "Micellization Behavior of Poly(n-butyl methacrylate)-block-poly(2-(acetoacetoxy)ethyl methacrylate)." Macromolecules 42, no. 12 (2009): 4257–61. http://dx.doi.org/10.1021/ma9003727.

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37

Özdemir, F., and S. Çavuş. "Poly(dodecyl methacrylate-co-2-(diethylamino)ethyl methacrylate) Gels: Characterization and Solubility Parameters." Acta Physica Polonica A 137, no. 4 (2020): 519–22. http://dx.doi.org/10.12693/aphyspola.137.519.

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38

Lu, Beibei, Lei Li, Lulu Wei, Xuhong Guo, Jun Hou та Zhiyong Liu. "Synthesis and thermo-responsive self-assembly behavior of amphiphilic copolymer β-CD–(PCL–P(MEO2MA-co-PEGMA))21 for the controlled intracellular delivery of doxorubicin". RSC Advances 6, № 56 (2016): 50993–1004. http://dx.doi.org/10.1039/c6ra08108h.

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Well-defined amphiphilic β-cyclodextrin star-shaped copolymers with poly(ε-caprolactone)–poly(2-(2-methoxyethoxy)ethyl methacrylate)-co-poly(ethylene glycol)methacrylate) (β-CD–(PCL–P(MEO<sub>2</sub>MA-co-PEGMA))<sub>21</sub> were synthesized via (ROP) and (ATRP).
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39

Erol, Ibrahim, and Cengiz Soykan. "Free-radical-initiated copolymerization of 2-(2-naphthylamino)-2-oxo-ethyl methacrylate with methyl methacrylate and styrene." Polymer International 53, no. 9 (2004): 1235–44. http://dx.doi.org/10.1002/pi.1466.

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40

Schovanec, Martin, Jiří Horálek, Štěpán Podzimek, and Jaromír Šňupárek. "Copolymerization of 2-[3-(2H-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl Methacrylate with Styrene." Collection of Czechoslovak Chemical Communications 72, no. 9 (2007): 1244–54. http://dx.doi.org/10.1135/cccc20071244.

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Radical copolymerization of 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate (M1) with styrene (M2) at 70 °C in 1,4-dioxane was investigated and the reactivity ratios were determined. The copolymerization was carried out as batch copolymerization to a low conversion or as copolymerization with a continuous addition of monomers at higher instantaneous conversion. The monomer reactivity ratios of the copolymerizable UV stabilizer 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate with styrene were determined using the Finemann-Ross plot for both copolymeration technique
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41

Wang, Fang Ping, Ting Yuan, Wan Xia Li, Jun Ying Zhang, and Qi Zhao Wang. "Synthesis and Characterization of Amphiphilic Copolymer Poly[2-(dimethylamino)ethyl methacrylate-co-methyl methacrylate]." Advanced Materials Research 936 (June 2014): 776–79. http://dx.doi.org/10.4028/www.scientific.net/amr.936.776.

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A novel, well-defined, amphiphilic block copolymer was synthesized by RAFT copolymerization of 2-(dimethylamino) ethyl methacrylate (DMAEMA) and methyl methacrylate (MMA). The polymer structure was characterized by1H NMR, GPC and TEM. It was found that the stable spherical micelles with core-shell structure are formed and good solubility in water. The copolymer would have great potential in drug delivery systems.
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42

Zhang, Xuan, Jianhui Xia, and Krzysztof Matyjaszewski. "Controlled/“Living” Radical Polymerization of 2-(Dimethylamino)ethyl Methacrylate." Macromolecules 31, no. 15 (1998): 5167–69. http://dx.doi.org/10.1021/ma980477j.

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43

Přádný, Martin, Stanislav Ševčík, and Stela Dragan. "Kinetics of quaternization reactions of polymeric amines." Collection of Czechoslovak Chemical Communications 54, no. 3 (1989): 663–72. http://dx.doi.org/10.1135/cccc19890663.

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The paper deals with kinetics phenomena occurring in the quaternization of some polymeric amines, such as poly[2-(dimethylamino)ethyl methacrylate], poly{N-[3-(dimethylamino)propyl]-acrylamide}, and poly[2-(dimethylamino)ethyl methacrylate-co-2-hydroxyethyl methacrylate], with alkyl halides. The accelerating and slowing-down effects which take place in the alkylation reactions are discussed on the basis of the reaction course, i.e. of the dependence of differential rate constants on the conversion fraction of the reaction. Accelaration of the reaction is affected by the increasing polarity of
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44

Chekurov, K. E., A. I. Barabanova, I. V. Blagodatskikh, et al. "Omniphobic Coatings Based on Amphiphilic Diblock Copolymers of 2-(Perfluorohexyl)ethyl Methacrylate and 2-Hydroxyethyl Methacrylate." Doklady Chemistry 496, no. 1 (2021): 18–23. http://dx.doi.org/10.1134/s0012500821010018.

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45

Jin, Xiaopin, Youqing Shen, and Shiping Zhu. "Atom Transfer Radical Block Copolymerization of 2-(N,N-Dimethylamino)ethyl Methacrylate and 2-Hydroxyethyl Methacrylate." Macromolecular Materials and Engineering 288, no. 12 (2003): 925–35. http://dx.doi.org/10.1002/mame.200300198.

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46

Grigale-Soročina, Zane, Elina Vindedze, Julija Kozela, and Ingmārs Birks. "Evaluation of Reactive Diluent Impact on Stability of Systems Viscosity in UV-Curable Compositions." Solid State Phenomena 320 (June 30, 2021): 150–54. http://dx.doi.org/10.4028/www.scientific.net/ssp.320.150.

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Abstract:
This study investigated the impact of various reactive diluents on viscosity of uncured mixture at 50 °C over a 12-week period. This criterion is important to predict the shelf life of uncured composition. Studied mono-functional acrylate monomers were: hydroxypropyl methacrylate (HPMA), hydroxyethyl methacrylate (HEMA), tetrahydrofurfuryl acrylate (THFA), isobornyl methacrylate (IBOMA), isobornyl acrylate (IBOA), 2-(2-Ethoxyethoxy)ethyl acrylate (EOEOEA), acryloyl morpholine (ACMO), glacial methacrylic acid (GMAA) and phosphate acrylate monomer (PAM); and various solvents: isopropanol(IP) eth
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Weber, Christine, Remzi C. Becer, Anja Baumgaertel, Richard Hoogenboom, and Ulrich S. Schubert. "Preparation of Methacrylate End-Functionalized Poly(2-ethyl-2-oxazoline) Macromonomers." Designed Monomers and Polymers 12, no. 2 (2009): 149–65. http://dx.doi.org/10.1163/156855509x412090.

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García, F., J. M. García, F. Rubio, J. L. de la Peña, J. Guzmán, and E. Riande. "Reaction kinetics and gel effect on the polymerization of 2-ethoxyethyl methacrylate and 2(2-ethoxyethoxy) ethyl methacrylate." Journal of Polymer Science Part A: Polymer Chemistry 40, no. 22 (2002): 3987–4001. http://dx.doi.org/10.1002/pola.10480.

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Baines, Fiona L., Steven P. Armes, Norman C. Billingham, and Zdenek Tuzar. "Micellization of Poly(2-(dimethylamino)ethyl methacrylate-block-methyl methacrylate) Copolymers in Aqueous Solution." Macromolecules 29, no. 25 (1996): 8151–59. http://dx.doi.org/10.1021/ma960740l.

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Bütün, Vural, Steven P. Armes, and Norman C. Billingham. "Selective Quaternization of 2-(Dimethylamino)ethyl Methacrylate Residues in Tertiary Amine Methacrylate Diblock Copolymers." Macromolecules 34, no. 5 (2001): 1148–59. http://dx.doi.org/10.1021/ma001550k.

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