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Artigos de revistas sobre o tema "MADIX controlled radical polymerization"

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Autor: Grafiati

Publicado: 25 de maio de 2024

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1

Etchenausia, Laura, Abdel Khoukh, Elise Deniau Lejeune e Maud Save. "RAFT/MADIX emulsion copolymerization of vinyl acetate and N-vinylcaprolactam: towards waterborne physically crosslinked thermoresponsive particles". Polymer Chemistry 8, n.º 14 (2017): 2244–56. http://dx.doi.org/10.1039/c7py00221a.

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2

Destarac, Mathias, Wojciech Bzducha, Daniel Taton, Isabelle Gauthier-Gillaizeau e Samir Z. Zard. "Xanthates as Chain-Transfer Agents in Controlled Radical Polymerization (MADIX): Structural Effect of the O-Alkyl Group". Macromolecular Rapid Communications 23, n.º 17 (dezembro de 2002): 1049–54. http://dx.doi.org/10.1002/marc.200290002.

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3

Destarac, Mathias, Juliette Ruchmann-Sternchuss, Eric Van Gramberen, Xavier Vila e Samir Z. Zard. "α-Amido Trifluoromethyl Xanthates: A New Class of RAFT/MADIX Agents". Molecules 29, n.º 10 (7 de maio de 2024): 2174. http://dx.doi.org/10.3390/molecules29102174.

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Xanthates have long been described as poor RAFT/MADIX agents for styrene polymerization. Through the determination of chain transfer constants to xanthates, this work demonstrated beneficial capto-dative substituent effects for the leaving group of a new series of α-amido trifluoromethyl xanthates, with the best effect observed with trifluoroacetyl group. The previously observed Z-group activation with a O-trifluoroethyl group compared to the O-ethyl counterpart was quantitatively established with Cex = 2.7 (3–4 fold increase) using the SEC peak resolution method. This study further confirmed the advantageous incorporation of trifluoromethyl substituents to activate xanthates in radical chain transfer processes and contributed to identify the most reactive xanthate reported to date for RAFT/MADIX polymerization of styrene.

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4

Seiler, Lucie, Julien Loiseau, Frédéric Leising, Pascal Boustingorry, Simon Harrisson e Mathias Destarac. "Acceleration and improved control of aqueous RAFT/MADIX polymerization of vinylphosphonic acid in the presence of alkali hydroxides". Polymer Chemistry 8, n.º 25 (2017): 3825–32. http://dx.doi.org/10.1039/c7py00747g.

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5

Wang, Pucheng, Jingwen Dai, Lei Liu, Qibao Dong, Hu Wang e Ruke Bai. "Synthesis and properties of a well-defined copolymer of chlorotrifluoroethylene and N-vinylpyrrolidone by xanthate-mediated radical copolymerization under 60Co γ-ray irradiation". Polym. Chem. 5, n.º 21 (2014): 6358–64. http://dx.doi.org/10.1039/c4py00902a.

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6

Theis, Alexander, Thomas P. Davis, Martina H. Stenzel e Christopher Barner-Kowollik. "Probing the reaction kinetics of vinyl acetate free radical polymerization via living free radical polymerization (MADIX)". Polymer 47, n.º 4 (fevereiro de 2006): 999–1010. http://dx.doi.org/10.1016/j.polymer.2005.12.054.

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7

Matyjaszewski, Krzysztof. "Controlled radical polymerization". Current Opinion in Solid State and Materials Science 1, n.º 6 (dezembro de 1996): 769–76. http://dx.doi.org/10.1016/s1359-0286(96)80101-x.

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8

Gaynor, Scott, Dorota Greszta, Daniela Mardare, Mircea Teodorescu e Krzysztof Matyjaszewski. "Controlled Radical Polymerization". Journal of Macromolecular Science, Part A 31, n.º 11 (janeiro de 1994): 1561–78. http://dx.doi.org/10.1080/10601329408545868.

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9

Bertin, Denis, e Bernard Boutevin. "Controlled radical polymerization". Polymer Bulletin 37, n.º 3 (setembro de 1996): 337–44. http://dx.doi.org/10.1007/bf00318066.

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10

Zard, Samir Z. "The Genesis of the Reversible Radical Addition–Fragmentation–Transfer of Thiocarbonylthio Derivatives from the Barton–McCombie Deoxygenation: A Brief Account and Some Mechanistic Observations". Australian Journal of Chemistry 59, n.º 10 (2006): 663. http://dx.doi.org/10.1071/ch06263.

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The observations and reasoning leading to the discovery of the degenerative transfer of xanthates and related thiocarbonylthio derivatives are briefly described. A few synthetic applications are presented, and the consequences on the emergence of the RAFT and MADIX polymerization technologies as well as some mechanistic aspects are briefly discussed.

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11

Lou, Yu, Dong Jian Shi, Wei Fu Dong e Ming Qing Chen. "Synthesis and Self-Assemble Behavior of Block Copolymerization of Vinyl Acetate and N-Vinylacetamide". Advanced Materials Research 645 (janeiro de 2013): 10–14. http://dx.doi.org/10.4028/www.scientific.net/amr.645.10.

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Polymerizations of VAc was carried out using AIBN as the initiator and DIP as the MADIX agent precursor. Then, block copolymer PVAc-b-PNVA had been synthesized by RAFT radical polymerization in the presence of PVAc-DIP as macro CTA. The length of blocks could be tuned by changing the molar ratio of NVA and VAc. Block copolymer PVAc-b-PNVA self-assembled into micelles in solution, and underwent microphase separation in bulk state.

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12

Severin, K., M. Haas, E. Solari, O. Nguyen, S. Gautier e R. Scopelliti. "RT-Controlled Radical Polymerization". Synfacts 2006, n.º 5 (maio de 2006): 0446. http://dx.doi.org/10.1055/s-2006-934385.

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13

Matyjaszewski, Krzysztof, e James Spanswick. "Controlled/living radical polymerization". Materials Today 8, n.º 3 (março de 2005): 26–33. http://dx.doi.org/10.1016/s1369-7021(05)00745-5.

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14

Pan, Xiangcheng, Mehmet Atilla Tasdelen, Joachim Laun, Thomas Junkers, Yusuf Yagci e Krzysztof Matyjaszewski. "Photomediated controlled radical polymerization". Progress in Polymer Science 62 (novembro de 2016): 73–125. http://dx.doi.org/10.1016/j.progpolymsci.2016.06.005.

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15

Tasdelen, Mehmet Atilla, Mustafa Uygun e Yusuf Yagci. "Photoinduced Controlled Radical Polymerization". Macromolecular Rapid Communications 32, n.º 1 (31 de agosto de 2010): 58–62. http://dx.doi.org/10.1002/marc.201000351.

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16

Bon, Stefan A. F., Michiel Bosveld, Bert Klumperman e Anton L. German. "Controlled Radical Polymerization in Emulsion". Macromolecules 30, n.º 2 (janeiro de 1997): 324–26. http://dx.doi.org/10.1021/ma961003s.

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17

Matyjaszewski, Krzysztof, Scott Gaynor, Dorota Greszta, Daniela Mardare e Takeo Shigemoto. "?Living? and controlled radical polymerization". Journal of Physical Organic Chemistry 8, n.º 4 (abril de 1995): 306–15. http://dx.doi.org/10.1002/poc.610080414.

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18

Whitfield, Richard, Nghia P. Truong e Athina Anastasaki. "Sequence-controlled Polymers via Controlled Radical Polymerization". CHIMIA International Journal for Chemistry 73, n.º 4 (24 de abril de 2019): 331. http://dx.doi.org/10.2533/chimia.2019.331.

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19

Caille, Jean-Raphaël, Antoine Debuigne e Robert Jérôme. "Controlled Radical Polymerization of Styrene by Quinone Transfer Radical Polymerization (QTRP)". Macromolecules 38, n.º 1 (janeiro de 2005): 27–32. http://dx.doi.org/10.1021/ma048561o.

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20

Matyjaszewski, Krzysztof. "Transition Metal Catalysis in Controlled Radical Polymerization: Atom Transfer Radical Polymerization". Chemistry - A European Journal 5, n.º 11 (5 de novembro de 1999): 3095–102. http://dx.doi.org/10.1002/(sici)1521-3765(19991105)5:11<3095::aid-chem3095>3.0.co;2-#.

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21

Wang, Lu, Wang e Bai. "A New Strategy for the Synthesis of Fluorinated Polyurethane". Polymers 11, n.º 9 (2 de setembro de 2019): 1440. http://dx.doi.org/10.3390/polym11091440.

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An alternating fluorinated copolymer based on chlorotrifluoroethylene (CTFE) and butyl vinyl ether (BVE) was synthesized by RAFT/MADIX living/controlled polymerization in the presence of S-benzyl O-ethyl dithiocarbonate (BEDTC). Then, using the obtained poly(CTFE-alt-BVE) as a macro chain transfer agent (macro-CTA), a block copolymer was prepared by chain extension polymerization of vinyl acetate (VAc). After a basic methanolysis process, the poly(vinyl acetate) (PVAc) block was transferred into poly(vinyl alcohol) (PVA). Finally, a novel fluorinated polyurethane with good surface properties due to the mobility of the flexible fluorinated polymer chains linked to the network was obtained via reaction of the copolymer bearing the blocks of PVA with isophorone diisocyanate (IPDI) as a cross-linking agent.

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22

Grimaud, Thomas, e Krzysztof Matyjaszewski. "Controlled/“Living” Radical Polymerization of Methyl Methacrylate by Atom Transfer Radical Polymerization". Macromolecules 30, n.º 7 (abril de 1997): 2216–18. http://dx.doi.org/10.1021/ma961796i.

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23

Xia, Jianhui, e Krzysztof Matyjaszewski. "Controlled/“Living” Radical Polymerization. Atom Transfer Radical Polymerization Using Multidentate Amine Ligands". Macromolecules 30, n.º 25 (dezembro de 1997): 7697–700. http://dx.doi.org/10.1021/ma971009x.

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24

Higashimura, Hideyuki. "Radical-Controlled Oxidative Polymerization of Phenols". Journal of Synthetic Organic Chemistry, Japan 63, n.º 10 (2005): 970–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.63.970.

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25

UEDA, Naoki. "Controlled Radical Polymerization with Iodine Compounds". Kobunshi 48, n.º 7 (1999): 513. http://dx.doi.org/10.1295/kobunshi.48.513.

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26

SHIGA, Akinobu. "“Radical -Controlled”Oxidative Polymerization of Phenols". Kobunshi 49, n.º 4 (2000): 236. http://dx.doi.org/10.1295/kobunshi.49.236.

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27

Matyjaszewski, K., e E. Chernikova. "New trends in controlled radical polymerization". Polymer Science Series C 57, n.º 1 (7 de julho de 2015): 1–2. http://dx.doi.org/10.1134/s1811238215010075.

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28

Pan, Xiangcheng, Marco Fantin, Fang Yuan e Krzysztof Matyjaszewski. "Externally controlled atom transfer radical polymerization". Chemical Society Reviews 47, n.º 14 (2018): 5457–90. http://dx.doi.org/10.1039/c8cs00259b.

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ATRP can be externally controlled by electrical current, light, mechanical forces and various chemical reducing agents. The mechanistic aspects and preparation of polymers with complex functional architectures and their applications are critically reviewed.

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29

Cuthbert, Julia, Anna C. Balazs, Tomasz Kowalewski e Krzysztof Matyjaszewski. "STEM Gels by Controlled Radical Polymerization". Trends in Chemistry 2, n.º 4 (abril de 2020): 341–53. http://dx.doi.org/10.1016/j.trechm.2020.02.002.

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30

Bruno, Ameduri. "Controlled Radical (Co)polymerization of Fluoromonomers". Macromolecules 43, n.º 24 (28 de dezembro de 2010): 10163–84. http://dx.doi.org/10.1021/ma1019297.

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31

Ameduri, Bruno. "Controlled Radical (Co)polymerization of Fluoromonomers". Macromolecules 44, n.º 7 (12 de abril de 2011): 2394. http://dx.doi.org/10.1021/ma2003536.

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32

Allen, Michael H., Sean T. Hemp, Adam E. Smith e Timothy E. Long. "Controlled Radical Polymerization of 4-Vinylimidazole". Macromolecules 45, n.º 9 (25 de abril de 2012): 3669–76. http://dx.doi.org/10.1021/ma300543h.

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33

Ansong, Omari E., Susan Jansen, Yen Wei, Gregory Pomrink, Hui Lu, Alpa Patel e Shuxi Li. "Accelerated controlled radical polymerization of methacrylates". Polymer International 58, n.º 1 (18 de novembro de 2008): 54–65. http://dx.doi.org/10.1002/pi.2492.

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34

Bohrisch, Jörg, Ulrich Wendler e Werner Jaeger. "Controlled radical polymerization of 4-vinylpyridine". Macromolecular Rapid Communications 18, n.º 11 (novembro de 1997): 975–82. http://dx.doi.org/10.1002/marc.1997.030181104.

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35

Charmot, D., P. Corpart, H. Adam, S. Z. Zard, T. Biadatti e G. Bouhadir. "Controlled radical polymerization in dispersed media". Macromolecular Symposia 150, n.º 1 (fevereiro de 2000): 23–32. http://dx.doi.org/10.1002/1521-3900(200002)150:1<23::aid-masy23>3.0.co;2-e.

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36

Matyjaszewski, Krzysztof. "Environmental aspects of controlled radical polymerization". Macromolecular Symposia 152, n.º 1 (março de 2000): 29–42. http://dx.doi.org/10.1002/1521-3900(200003)152:1<29::aid-masy29>3.0.co;2-c.

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37

Tamasi, Matthew, Shashank Kosuri, Jason DiStefano, Robert Chapman e Adam J. Gormley. "Automation of Controlled/Living Radical Polymerization". Advanced Intelligent Systems 2, n.º 2 (29 de janeiro de 2020): 1900126. http://dx.doi.org/10.1002/aisy.201900126.

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38

Schmidt-Naake, Gudrun, Marco Drache e Carsten Taube. "TEMPO-controlled free radical suspension polymerization". Die Angewandte Makromolekulare Chemie 265, n.º 1 (1 de março de 1999): 62–68. http://dx.doi.org/10.1002/(sici)1522-9505(19990301)265:1<62::aid-apmc62>3.0.co;2-p.

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39

Steenbock, M., M. Klapper e K. Müllen. "“Self-regulation” of controlled radical polymerization". Acta Polymerica 49, n.º 7 (julho de 1998): 376–78. http://dx.doi.org/10.1002/(sici)1521-4044(199807)49:7<376::aid-apol376>3.0.co;2-e.

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40

Jin, Xin, Hongliang Kang, Ruigang Liu e Yong Huang. "Controlled radical emulsion polymerization of polystyrene". Colloid and Polymer Science 291, n.º 10 (9 de junho de 2013): 2481–85. http://dx.doi.org/10.1007/s00396-013-2998-6.

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41

Kavitha, Amalin A., Anusuya Choudhury e Nikhil K. Singha. "Controlled Radical Polymerization of Furfuryl Methacrylate". Macromolecular Symposia 240, n.º 1 (julho de 2006): 232–37. http://dx.doi.org/10.1002/masy.200650828.

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42

Özyürek, Zeynep, Hartmut Komber, Stefan Gramm, Dirk Schmaljohann, Axel H. E. Müller e Brigitte Voit. "Thermoresponsive Glycopolymers via Controlled Radical Polymerization". Macromolecular Chemistry and Physics 208, n.º 10 (21 de maio de 2007): 1035–49. http://dx.doi.org/10.1002/macp.200600661.

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43

Tasdelen, Mehmet Atilla, Mustafa Uygun e Yusuf Yagci. "Photoinduced Controlled Radical Polymerization in Methanol". Macromolecular Chemistry and Physics 211, n.º 21 (30 de setembro de 2010): 2271–75. http://dx.doi.org/10.1002/macp.201000445.

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44

Jenkins, Aubrey D., Richard G. Jones e Graeme Moad. "Terminology for reversible-deactivation radical polymerization previously called "controlled" radical or "living" radical polymerization (IUPAC Recommendations 2010)". Pure and Applied Chemistry 82, n.º 2 (18 de novembro de 2009): 483–91. http://dx.doi.org/10.1351/pac-rep-08-04-03.

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This document defines terms related to modern methods of radical polymerization, in which certain additives react reversibly with the radicals, thus enabling the reactions to take on much of the character of living polymerizations, even though some termination inevitably takes place. In recent technical literature, these reactions have often been loosely referred to as, inter alia, "controlled", "controlled/living", or "living" polymerizations. The use of these terms is discouraged. The use of "controlled" is permitted as long as the type of control is defined at its first occurrence, but the full name that is recommended for these polymerizations is "reversible-deactivation radical polymerization".

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45

Quiclet-Sire, Béatrice, e Samir Z. Zard. "Fun with radicals: Some new perspectives for organic synthesis". Pure and Applied Chemistry 83, n.º 3 (15 de outubro de 2010): 519–51. http://dx.doi.org/10.1351/pac-con-10-08-07.

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The degenerative radical addition-transfer of xanthates onto alkenes allows the rapid assembly of richly functionalized structures. Various families of open-chain, cyclic, and polycyclic compounds can thus be readily accessed. Furthermore, the process can be extended to the synthesis or modification of aromatic and heteroaromatic derivatives by exploiting the possibility of using peroxides both as initiators and stoichiometric oxidants. The modification of existing polymers and the controlled synthesis of block polymers by what is now known as the RAFT/MADIX (reversible addition–fragmentation transfer/macromolecular design by interchange of xanthate) process is described briefly.

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46

Yaǧci, Yusuf, Ayşegül Başkan Düz e Ayşen Önen. "Controlled radical polymerization initiated by stable radical terminated polytetrahydrofuran". Polymer 38, n.º 11 (maio de 1997): 2861–63. http://dx.doi.org/10.1016/s0032-3861(97)85626-1.

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47

Xia, Jianhui, Scott G. Gaynor e Krzysztof Matyjaszewski. "Controlled/“Living” Radical Polymerization. Atom Transfer Radical Polymerization of Acrylates at Ambient Temperature". Macromolecules 31, n.º 17 (agosto de 1998): 5958–59. http://dx.doi.org/10.1021/ma980725b.

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48

Save, Maud, Yohann Guillaneuf e Robert G. Gilbert. "Controlled Radical Polymerization in Aqueous Dispersed Media". Australian Journal of Chemistry 59, n.º 10 (2006): 693. http://dx.doi.org/10.1071/ch06308.

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Controlled radical polymerization (CRP), sometimes also termed ‘living’ radical polymerization, offers the potential to create a wide range of polymer architectures, and its implementation in aqueous dispersed media (e.g. emulsion polymerization, used on a vast scale industrially) opens the way to large-scale manufacture of products based on this technique. Until recently, implementing CRP in aqueous dispersed media was plagued with problems such as loss of ‘living’ character and loss of colloidal stability. This review examines the basic mechanistic processes in free-radical polymerization in aqueous dispersed media (e.g. emulsion polymerization), and then examines, through this mechanistic understanding, the new techniques that have been developed over the last few years to implement CRP successfully in emulsion polymerizations and related processes. The strategies leading to these successes can thus be understood in terms of the various mechanisms which dominate CRP systems in dispersed media; these mechanisms are sometimes quite different from those in conventional free-radical polymerization in these media.

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49

Xue, Wentao, Jie Wang, Ming Wen, Gaojian Chen e Weidong Zhang. "Integration of CuAAC Polymerization and Controlled Radical Polymerization into Electron Transfer Mediated “Click-Radical” Concurrent Polymerization". Macromolecular Rapid Communications 38, n.º 6 (3 de fevereiro de 2017): 1600733. http://dx.doi.org/10.1002/marc.201600733.

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50

Sütekin, S. Duygu, e Olgun Güven. "Radiation-induced controlled polymerization of acrylic acid by RAFT and RAFT-MADIX methods in protic solvents". Radiation Physics and Chemistry 142 (janeiro de 2018): 82–87. http://dx.doi.org/10.1016/j.radphyschem.2017.01.046.

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