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Journal articles on the topic 'Poly(glycidyl methacrylate) RAFT'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Docherty, Philip J., Chloé Girou, Matthew J. Derry, and Steven P. Armes. "Epoxy-functional diblock copolymer spheres, worms and vesicles via polymerization-induced self-assembly in mineral oil." Polymer Chemistry 11, no. 19 (2020): 3332–39. http://dx.doi.org/10.1039/d0py00380h.

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2

Docherty, Philip J., Matthew J. Derry, and Steven P. Armes. "RAFT dispersion polymerization of glycidyl methacrylate for the synthesis of epoxy-functional block copolymer nanoparticles in mineral oil." Polymer Chemistry 10, no. 5 (2019): 603–11. http://dx.doi.org/10.1039/c8py01584h.

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Epoxy-functional poly(stearyl methacrylate)-poly(glycidyl methacrylate) (PSMA-PGlyMA) diblock copolymer nanoparticles are synthesized via reversible addition–fragmentation chain transfer (RAFT) dispersion polymerization of glycidyl methacrylate (GlyMA) in mineral oil at 70 °C.

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3

Lan, Daosong, Lei Xiong, Hongtao Wanyan, et al. "Poly(glycidyl Methacrylate) Grafted to Carbon Fiber Surface by RAFT Polymerization for Enhancing Interface Adhesion and Mechanical Properties of Carbon Fiber/Epoxy Composites." Polymers and Polymer Composites 25, no. 1 (2017): 113–18. http://dx.doi.org/10.1177/096739111702500115.

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In this study, we present a novel approach to graft a large number of poly(glycidyl methacrylate) (PGMA) chains onto the carbon fiber (CF) surface through reversible addition-fragmentation chain transfer (RAFT) polymerization. Characterization results of FT-IR, XPS and TGA demonstrated that PGMA was covalently combined with carbon fibers. The CF/epoxy composites were obtained by addition of pristine CF and CF functionalized with poly(glycidyl methacrylate) (CF-PGMA) into epoxy resin. Experiment results revealed that the grafting of PGMA chains on the CF surface could increase significantly rou

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4

Kim, Seon-Mi, Sang Suk Han, A. Young Kim, et al. "Anti-Biofouling Effect of PEG-Grafted Block Copolymer Synthesized by RAFT Polymerization." Journal of Nanoscience and Nanotechnology 15, no. 10 (2015): 7866–70. http://dx.doi.org/10.1166/jnn.2015.11216.

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Poly(glycidyl methacrylate-block-styrene) (PGMA-b-PS), a block copolymer consisting of glycidyl methacrylate and styrene, was synthesized via reversible addition-fragmentation chain transfer living polymerization. The synthesized PGMA-b-PS was then grafted with low-molecular-weight polyethylene glycol (PEG) via epoxy ring opening to give PGMA-g-PEG-b-PS, which was evaluated as an anti-biofouling coating material. As a preliminary test for the anti-biofouling effect, a protein adsorption experiment was performed on the synthesized block copolymer surface. The block copolymers were spin-coated o

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5

Gudipati, Chakravarthy S., Maureen B. H. Tan, Hazrat Hussain, Ye Liu, Chaobin He, and Thomas P. Davis. "Synthesis of Poly(glycidyl methacrylate)-block-Poly(pentafluorostyrene) by RAFT: Precursor to Novel Amphiphilic Poly(glyceryl methacrylate)-block-Poly(pentafluorostyrene)." Macromolecular Rapid Communications 29, no. 23 (2008): 1902–7. http://dx.doi.org/10.1002/marc.200800515.

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6

Koubková, Jana, Hana Macková, Vladimír Proks, Miroslava Trchová, Jiří Brus, and Daniel Horák. "RAFT of sulfobetaine for modifying poly(glycidyl methacrylate) microspheres to reduce nonspecific protein adsorption." Journal of Polymer Science Part A: Polymer Chemistry 53, no. 19 (2015): 2273–84. http://dx.doi.org/10.1002/pola.27681.

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7

Thankappan, Hajeeth, Mona Semsarilar, Suming Li, Yung Chang, Denis Bouyer, and Damien Quemener. "Synthesis of Block Copolymer Brush by RAFT and Click Chemistry and Its Self-Assembly as a Thin Film." Molecules 25, no. 20 (2020): 4774. http://dx.doi.org/10.3390/molecules25204774.

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A well-defined block copolymer brush poly(glycidyl methacrylate)-graft-(poly(methyl methacrylate)-block- poly(oligo(ethylene glycol) methyl ether methacrylate)) (PGMA-g-(PMMA-b-POEGMA)) is synthesized via grafting from an approach based on a combination of click chemistry and reversible addition-fragmentation chain transfer (RAFT) polymerization. The resulting block copolymer brushes were characterized by 1H-NMR and size exclusion chromatography (SEC). The self-assembly of the block copolymer brush was then investigated under selective solvent conditions in three systems: THF/water, THF/CH3OH,

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8

Pourjavadi, Ali, Mohammad Kohestanian, and Mahshid Yaghoubi. "Poly(glycidyl methacrylate)-coated magnetic graphene oxide as a highly efficient nanocarrier: preparation, characterization, and targeted DOX delivery." New Journal of Chemistry 43, no. 47 (2019): 18647–56. http://dx.doi.org/10.1039/c9nj04623b.

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Herein, we report the preparation of novel magnetic graphene oxide grafted with brush polymer via SI-RAFT polymerization and its application as a nanocarrier for magnetic and pH-triggered delivery of DOX anticancer drug.

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9

Yin, Huiwen, Haimei Zheng, Lican Lu, Pengsheng Liu, and Yuanli Cai. "Highly efficient and well-controlled ambient temperature RAFT polymerization of glycidyl methacrylate under visible light radiation." Journal of Polymer Science Part A: Polymer Chemistry 45, no. 22 (2007): 5091–102. http://dx.doi.org/10.1002/pola.22251.

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10

Cao, Jun, Lifen Zhang, Xiangqiang Pan, Zhenping Cheng, and Xiulin Zhu. "RAFT Copolymerization of Glycidyl Methacrylate andN,N-Dimethylaminoethyl Methacrylate." Chinese Journal of Chemistry 30, no. 9 (2012): 2138–44. http://dx.doi.org/10.1002/cjoc.201200625.

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11

Rosales-Guzmán, Miguel, Odilia Pérez-Camacho, Carlos Guerrero-Sánchez, et al. "Semiautomated Parallel RAFT Copolymerization of Isoprene with Glycidyl Methacrylate." ACS Combinatorial Science 21, no. 12 (2019): 771–81. http://dx.doi.org/10.1021/acscombsci.9b00110.

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12

Zulfiqar, S., M. Zulfiqar, M. Nawaz, I. C. McNeill, and J. G. Gorman. "Thermal degradation of poly(glycidyl methacrylate)." Polymer Degradation and Stability 30, no. 2 (1990): 195–203. http://dx.doi.org/10.1016/0141-3910(90)90075-i.

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13

Grigoreva, Alexandra O., Kseniia Tarankova, and Sergey D. Zaitsev. "Copolymerization of Glycidyl Methacrylate and 1,1,1,3,3,3-Hexafluoroisopropyl Acrylate." Key Engineering Materials 899 (September 8, 2021): 387–91. http://dx.doi.org/10.4028/www.scientific.net/kem.899.387.

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The copolymerization of 1,1,1,3,3,3-hexafluoroisopropyl acrylate (HFIPA) and glycidyl methacrylate via reversible addition-fragmentation chain transfer (RAFT) process was investigated. 2-cyano-2-propyl dodecyl trithiocarbonate (CPDT) was used as chain transfer agent. It is turned out that CPDT and polymeric chain transfer agent obtained based on HFIPA and CPDT provide a good control over molar mass characteristic of copolymers (Đ = 1.05). Reactivity ratios were found to be r1(GMA) = 1.57 and r2(HFIPA) = 0.05 by Fineman–Ross model.

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14

Gohy, Jean-François, Sayed Antoun, and Robert Jérôme. "Self-aggregation of poly(methyl methacrylate)-block-poly(sulfonated glycidyl methacrylate) copolymers." Polymer 42, no. 21 (2001): 8637–45. http://dx.doi.org/10.1016/s0032-3861(01)00375-5.

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15

Xun, Weiwei, Yulin Yi, Chongyin Zhang та Sixun Zheng. "Poly(glycidyl methacrylate)-block-poly(ϵ-caprolactone)-block-poly(glycidyl methacrylate) Triblock Copolymer: Synthesis and Use as Mesoporous Silica Porogen". Journal of Macromolecular Science, Part A 50, № 4 (2013): 399–410. http://dx.doi.org/10.1080/10601325.2013.768152.

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16

Aprilita, Nurul H., Christian W. Huck, Rania Bakry, et al. "Poly(Glycidyl Methacrylate/Divinylbenzene)-IDA-FeIIIin Phosphoproteomics." Journal of Proteome Research 4, no. 6 (2005): 2312–19. http://dx.doi.org/10.1021/pr050224m.

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17

Caykara, Tuncer, Ferhat Çakar, and Serkan Demirci. "Preparation of amidoximated poly(glycidyl methacrylate) microbeads." Polymer International 60, no. 1 (2010): 141–45. http://dx.doi.org/10.1002/pi.2923.

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18

Grama, Silvia, Nataliya Boiko, Rostyslav Bilyy, et al. "Novel fluorescent poly(glycidyl methacrylate) – Silica microspheres." European Polymer Journal 56 (July 2014): 92–104. http://dx.doi.org/10.1016/j.eurpolymj.2014.04.011.

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19

Horák, Daniel, Jaroslav Straka, Bohdan Schneider, František Lednický, and Jan Pilař. "Poly(ethylene dimethacrylate) particles with poly(glycidyl methacrylate) functionalities." Polymer 35, no. 6 (1994): 1195–202. http://dx.doi.org/10.1016/0032-3861(94)90011-6.

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20

Hatton, Fiona L., Matthew J. Derry, and Steven P. Armes. "Rational synthesis of epoxy-functional spheres, worms and vesicles by RAFT aqueous emulsion polymerisation of glycidyl methacrylate." Polymer Chemistry 11, no. 39 (2020): 6343–55. http://dx.doi.org/10.1039/d0py01097a.

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The rational synthesis of epoxy-functional diblock copolymer nano-objects has been achieved by RAFT aqueous emulsion polymerisation of glycidyl methacrylate under mild conditions (50 °C, pH 7) to preserve the epoxy groups.

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21

Hatton, Fiona L., Joseph R. Lovett, and Steven P. Armes. "Synthesis of well-defined epoxy-functional spherical nanoparticles by RAFT aqueous emulsion polymerization." Polymer Chemistry 8, no. 33 (2017): 4856–68. http://dx.doi.org/10.1039/c7py01107e.

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The environmentally-friendly synthesis of epoxy-functional spherical nanoparticles is achieved via RAFT aqueous emulsion polymerization of glycidyl methacrylate under mild conditions; derivatization of such nanoparticles with sodium azide or diamines is demonstrated.

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22

Mohammed Safiullah, S., K. Abdul Wasi, and K. Anver Basha. "Poly(glycidyl methacrylate)—A soft template for the facile preparation of poly(glycidyl methacrylate) core-copper nanoparticle shell nanocomposite." Applied Surface Science 357 (December 2015): 112–21. http://dx.doi.org/10.1016/j.apsusc.2015.08.254.

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23

Chong, Bill, Graeme Moad, Ezio Rizzardo, Melissa Skidmore, and San H. Thang. "Thermolysis of RAFT-Synthesized Poly(Methyl Methacrylate)." Australian Journal of Chemistry 59, no. 10 (2006): 755. http://dx.doi.org/10.1071/ch06229.

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Thermolysis provides a simple and efficient way of eliminating thiocarbonylthio groups from RAFT-synthesized polymers. The course of thermolysis of poly(methyl methacrylate) (PMMA) prepared with dithiobenzoate and trithiocarbonate RAFT agents was followed by thermogravimetric analysis (TGA), 1H NMR spectroscopy, and gel permeation chromatography (GPC). The weight loss profile observed depends strongly on the RAFT agent used during polymer synthesis. PMMA with a methyl trithiocarbonate end group undergoes loss of that end group at ~180°C, at least in part, by a mechanism believed to involve hom

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24

Lee, Seung No, Moon Yeon Lee, and Won Ho Park. "Thermal stabilization of poly(3-hydroxybutyrate) by poly(glycidyl methacrylate)." Journal of Applied Polymer Science 83, no. 13 (2002): 2945–52. http://dx.doi.org/10.1002/app.10318.

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25

Kihara, Nobuhiro, and Takeshi Endo. "Incorporation of carbon dioxide into poly(glycidyl methacrylate)." Macromolecules 25, no. 18 (1992): 4824–25. http://dx.doi.org/10.1021/ma00044a053.

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26

Koubková, Jana, Petr Müller, Helena Hlídková, et al. "Magnetic poly(glycidyl methacrylate) microspheres for protein capture." New Biotechnology 31, no. 5 (2014): 482–91. http://dx.doi.org/10.1016/j.nbt.2014.06.004.

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27

Jang, Jyongsik, Joonwon Bae, and Sungrok Ko. "Synthesis and curing of poly(glycidyl methacrylate) nanoparticles." Journal of Polymer Science Part A: Polymer Chemistry 43, no. 11 (2005): 2258–65. http://dx.doi.org/10.1002/pola.20706.

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28

Vijayakumar, M. T., C. Rami Reddy, and K. T. Joseph. "Grafting of poly(glycidyl methacrylate) onto alginic acid." European Polymer Journal 21, no. 4 (1985): 415–19. http://dx.doi.org/10.1016/0014-3057(85)90201-0.

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29

Pavlínek, V., O. Quadrat, P. Sáha, M. J. Benes , and J. Trlica. "Electrorheological properties of hydrolyzed poly(glycidyl methacrylate) suspensions." Colloid & Polymer Science 276, no. 8 (1998): 690–97. http://dx.doi.org/10.1007/s003960050298.

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30

Gan, P. P., and D. R. Paul. "Blends of glycidyl methacrylate/methyl methacrylate copolymers with poly(vinylidene fluoride)." Journal of Polymer Science Part B: Polymer Physics 33, no. 11 (1995): 1693–703. http://dx.doi.org/10.1002/polb.1995.090331115.

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31

Goswami, Prodip K., Monsum Kashyap, Pranjal P. Das, Prakash J. Saikia, and Jyotirekha G. Handique. "Poly(Glycidyl Methacrylate-co-Octadecyl Methacrylate) particles by dispersion radical copolymerization." Journal of Dispersion Science and Technology 41, no. 12 (2019): 1768–76. http://dx.doi.org/10.1080/01932691.2019.1635026.

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32

Shao, Hui Ju, Jian Bing Guo, Yang Jun Li, Jie Yu, and Shu Hao Qin. "Reactive Grafting of Glycidyl Methacrylate onto Poly (Ethylene-1-Octene)." Advanced Materials Research 239-242 (May 2011): 1153–58. http://dx.doi.org/10.4028/www.scientific.net/amr.239-242.1153.

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Poly (ethylene-1-octene) (POE) was functionalized to varying degrees with glycidyl methacrylate (GMA) by melt grafting processes. Fourier transform infrared spectra (FT-IR) and 1H NMR spectra confirmed that glycidyl methacrylate was successfully grafted onto the POE. When dicumyl peroxide(DCP)concentration was around 4‰ high graft degree was obtained. The data from GPC measure demonstrates that POE chains degraded during grafting process.

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33

Zhou, Quan, Qi Liu, Ning Song, Jingyi Yang, and Lizhong Ni. "Amphiphilic reactive poly(glycidyl methacrylate)-block-poly(dimethyl siloxane)-block-poly(glycidyl methacrylate) triblock copolymer for the controlling nanodomain morphology of epoxy thermosets." European Polymer Journal 120 (November 2019): 109236. http://dx.doi.org/10.1016/j.eurpolymj.2019.109236.

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34

Horák, Daniel, Emil Pollert, and Hana Macková. "Properties of magnetic poly(glycidyl methacrylate) and poly(N-isopropylacrylamide) microspheres." Journal of Materials Science 43, no. 17 (2008): 5845–50. http://dx.doi.org/10.1007/s10853-008-2836-2.

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35

Thanh Nguyen, Hoang, and Tuan Manh Nguyen. "Investigation of Magnetic Properties of Magnetic Poly (glycidyl methacrylate) Microspheres: Experimental and Theoretical." Advances in Materials Science and Engineering 2021 (June 24, 2021): 1–10. http://dx.doi.org/10.1155/2021/6676453.

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Biocompatible magnetic poly (glycidyl methacrylate) microsphere is a novel nanocomposite with a myriad of promising bioapplications. Investigation of their characteristics by experimental analysis methods has also been carried out in the past. However, a survey of the magnetic anisotropy constant has not been mentioned and the influence of the poly (glycidyl methacrylate) polymer matrix on the Fe3O4 magnetite nanoparticles embedded inside has also not been discussed. Moreover, the accurate characterization of the magnetite nanoparticle size distribution remains challenging. In this paper, we p

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36

Nara, Saori, Hiroki Sagawa, Hiromu Saito, and Hideko T. Oyama. "Synergetic toughening of poly(phenylene sulfide) by poly(phenylsulfone) and poly(ethylene‐ ran ‐methacrylate‐ ran ‐glycidyl methacrylate)." Journal of Applied Polymer Science 138, no. 4 (2020): 49994. http://dx.doi.org/10.1002/app.49994.

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37

György, Csilla, Saul J. Hunter, Chloé Girou, Matthew J. Derry, and Steven P. Armes. "Synthesis of poly(stearyl methacrylate)-poly(2-hydroxypropyl methacrylate) diblock copolymer nanoparticles via RAFT dispersion polymerization of 2-hydroxypropyl methacrylate in mineral oil." Polymer Chemistry 11, no. 28 (2020): 4579–90. http://dx.doi.org/10.1039/d0py00562b.

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38

Muzammil, Ezzah M., Anzar Khan, and Mihaiela C. Stuparu. "Post-polymerization modification reactions of poly(glycidyl methacrylate)s." RSC Advances 7, no. 88 (2017): 55874–84. http://dx.doi.org/10.1039/c7ra11093f.

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39

Zhang, Minlian, and Yan Sun. "Poly(glycidyl methacrylate–divinylbenzene–triallylisocyanurate) continuous-bed protein chromatography." Journal of Chromatography A 912, no. 1 (2001): 31–38. http://dx.doi.org/10.1016/s0021-9673(01)00526-x.

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40

Yang, Yan-Yu, Hao Hu, Xing Wang, et al. "Acid-Labile Poly(glycidyl methacrylate)-Based Star Gene Vectors." ACS Applied Materials & Interfaces 7, no. 22 (2015): 12238–48. http://dx.doi.org/10.1021/acsami.5b02733.

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41

Marinović, S., Z. Vuković, A. Nastasović, A. Milutinović-Nikolić, and D. Jovanović. "Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate)/clay composites." Materials Chemistry and Physics 128, no. 1-2 (2011): 291–97. http://dx.doi.org/10.1016/j.matchemphys.2011.03.018.

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42

Chellapandian, M., and M. R. V. Krishnan. "Chitosan-poly (glycidyl methacrylate) copolymer for immobilization of urease." Process Biochemistry 33, no. 6 (1998): 595–600. http://dx.doi.org/10.1016/s0032-9592(98)80001-0.

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43

Horák, Daniel, Eduard Petrovský, Aleš Kapička, and Theodor Frederichs. "Synthesis and characterization of magnetic poly(glycidyl methacrylate) microspheres." Journal of Magnetism and Magnetic Materials 311, no. 2 (2007): 500–506. http://dx.doi.org/10.1016/j.jmmm.2006.08.006.

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44

Hor�k, Daniel, and Pavlo Shapoval. "Reactive poly(glycidyl methacrylate) microspheres prepared by dispersion polymerization." Journal of Polymer Science Part A: Polymer Chemistry 38, no. 21 (2000): 3855–63. http://dx.doi.org/10.1002/1099-0518(20001101)38:21<3855::aid-pola20>3.0.co;2-2.

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45

Willett, J. L., M. A. Kotnis, G. S. O'Brien, G. F. Fanta, and S. H. Gordon. "Properties of starch-graft-poly(glycidyl methacrylate)-PHBV composites." Journal of Applied Polymer Science 70, no. 6 (1998): 1121–27. http://dx.doi.org/10.1002/(sici)1097-4628(19981107)70:6<1121::aid-app8>3.0.co;2-q.

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46

Aprilita, Nurul Hidayat, Rania Bakry, Christian W. Huck, and Guenther K. Bonn. "POLY(GLYCIDYL METHACRYLATE-DIVINYLBENZENE) MONOLITHIC CAPILLARY AS A STATIONARY PHASE FOR THE REVERSED-PHASE CHROMATOGRAPHIC SEPARATION OF PROTEINS." Indonesian Journal of Chemistry 5, no. 1 (2010): 1–6. http://dx.doi.org/10.22146/ijc.21830.

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Capillary column with monolithic stationary phase was prepared from silanized fused-silica capillary of 200 µm I.D. by in situ free radical polymerization of divinylbenzene with glycidy methacrylate in the presence of decanol and tetrahydrofuran as porogens. The hydrodynamic and chromatographic properties of this monolith, such as backpressure at different flow-rate, pore size distribution, van Deemter plot and the effect of varying gradient-rate were investigated. Poly(glycidyl methacrylate-divinylbenzene) monolithic capillary has been used successfully for the reversed-phase chromatographic

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47

Feng Li, Ming Ma, Zhe-Fan Yuan, Jing-Yi Huang, and Ren-Xi Zhuo. "Novel poly(glycidyl methacrylate-b-propylene oxide-b-glycidyl methacrylate) derivatives with low cytotoxicity and efficient gene delivery." Journal of Bioactive and Compatible Polymers 26, no. 4 (2011): 388–404. http://dx.doi.org/10.1177/0883911511410461.

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48

Pei, Yiwen, Odilia R. Sugita, Luckshen Thurairajah, and Andrew B. Lowe. "Synthesis of poly(stearyl methacrylate-b-3-phenylpropyl methacrylate) nanoparticles in n-octane and associated thermoreversible polymorphism." RSC Advances 5, no. 23 (2015): 17636–46. http://dx.doi.org/10.1039/c5ra00274e.

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Poly(stearyl methacrylate) with average degrees of polymerization ranging from 18–30 were prepared by RAFT radical polymerization and then employed as macro-chain transfer agents in RAFT dispersion formulations with 3-phenylpropyl methacrylate as the comonomer.

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49

Ma, Yanli, Ling He, Aizhao Pan, and Chengben Zhao. "Poly(glycidyl methacrylate-POSS)-co-poly(methyl methacrylate) latex by epoxide opening reaction and emulsion polymerization." Journal of Materials Science 50, no. 5 (2014): 2158–66. http://dx.doi.org/10.1007/s10853-014-8778-y.

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50

Benvenuta-Tapia, Juan José, José Alfredo Tenorio-López, and Eduardo Vivaldo-Lima. "Estimation of Reactivity Ratios in the RAFT Copolymerization of Styrene and Glycidyl Methacrylate." Macromolecular Reaction Engineering 12, no. 5 (2018): 1800003. http://dx.doi.org/10.1002/mren.201800003.

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