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Radical addition–fragmentation chemistry in polymer synthesis
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This review traces the development of addition–fragmentation chain transfer agents and related ring-opening monomers highlighting recent innovation in these areas. The major part of this review deals with reagents that give reversible addition–fragmentation chain transfer (RAFT). These reagents include dithioesters, trithiocarbonates, dithiocarbamates and xanthates. The RAFT process is a versatile method for conferring living characteristics on radical polymerizations providing unprecedented control over molecular weight, molecular weight distribution, composition and architecture. It is suitable for most monomers polymerizable by radical polymerization and is robust under a wide range of reaction conditions. It provides a route to functional polymers, cyclopolymers, gradient copolymers, block polymers and star polymers.
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“In these reactions, β-scission of the intermediate radical formed upon radical addition to the sulfur atom of the C=S double bond plays a vital role (Figure 1A).”
From Direct Radical Copolymerizations of Thioamides To Generate Vinyl Polymers with Degradable Thioether Bonds in the Backbones (2023) · cites this paper as [2]
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“Thiocarbonyl compounds are fundamentally useful in radical chemistry and are extensively utilized to produce various molecules and macromolecules in reactions such as the Barton–McCombie reaction and reversible addition–fragmentation chain transfer (RAFT) polymerization.1−4”
From Direct Radical Copolymerizations of Thioamides To Generate Vinyl Polymers with Degradable Thioether Bonds in the Backbones (2023) · cites this paper as [2]
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Chiefari, J., Chong, Y. K. (., Ercole, F., Krstina, J., Jeffery, J. L., Le, T. P. T., Mayadunne, R. T. A., Meijs, G. F., Moad, C. L., Moad, G., et al. (1998) · Macromolecules · doi:10.1021/ma9804951 · Cited by 5,147
Self-citationControlled/living radical polymerization: Features, developments, and perspectives
Braunecker, W. A., & Matyjaszewski, K. (2007) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2006.11.002 · Cited by 3,202
Living Radical Polymerization by the RAFT Process
Moad, G., Rizzardo, E., & Thang, S. H. (2005) · Australian Journal of Chemistry · doi:10.1071/ch05072 · Cited by 2,286
Self-citationA new method for the deoxygenation of secondary alcohols
Barton, D. H. R., & McCombie, S. W. (1975) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19750001574 · Cited by 1,666
Handbook of Radical Polymerization
Matyjaszewski, K. A., & Davis, T. P. (2002) · Wiley eBooks · doi:10.1002/0471220450 · Cited by 1,595
Functional Polymers from Novel Carboxyl-Terminated Trithiocarbonates as Highly Efficient RAFT Agents
Lai, J. T., Filla, D., & Shea, R. (2002) · Macromolecules · doi:10.1021/ma020362m · Cited by 1,484
Perrier, S., & Takolpuckdee, P. (2005) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/pola.20986 · Cited by 1,157
Radicals in organic synthesis : formation of carbon-carbon bonds
Giese, B. (1986) · Pergamon Press eBooks · Cited by 1,083
Chong, ). Y. K., Le, T. P. T., Moad, G., Rizzardo, E., & Thang, S. H. (1999) · Macromolecules · doi:10.1021/ma981472p · Cited by 850
Self-citationLiving Radical Polymerization by the RAFT Process—A First Update
Moad, G., Rizzardo, E., & Thang, S. H. (2006) · Australian Journal of Chemistry · doi:10.1071/ch06250 · Cited by 847
Self-citation
Research works printed but not linked: 25
- Otsu, 1982, Polym Bull, 7, 45
- McCormick, 2006, Polym Rev, 46, 421
- Yakimansky, 2005, Polym Sci Ser C, 47, 1
- Golubev, 2005, Polym Sci Ser A, 47, 678
- Cho, 1990, J Polym Sci Part A Polym Chem, 28, 417
- Bailey WJ, Arfaei PY, Chen PY, Chen S-C, Endo T, Pan C-Y, et al. Proc. IUPAC 28th Macromol. Symp. Amherst, MA; 1982. p. 214.
- Sidney, 1981, Polym Prepr (Am Chem Soc Div Polym Chem), 22, 373
- Kobayashi, 1991, Macromol Rep, A28, 1
- Kobayashi, 1992, Macromol Rep, A29, 243
- Meijs, 1992, Polym Prepr (Am Chem Soc Div Polym Chem), 33, 893
- Chaumont, 1995, Macromol Chem Phys, 196, 947, 10.1002/macp.1995.021960322 · DOI
- Harrison DS. M.Sc. thesis. Hawthorn, Victoria: Swinburne University; 1988.
- Zhu, 2003, e-Polymers, 043
- Aoyagi, 2006, Synlett, 636
- Zhou, 2006, e-Polymers, 59
- Yu, 2007, e-Polymers
- Fox, 2003, Synlett, 2037
- You, 2002, Macromol Chem Phys, 203, 477, 10.1002/1521-3935(20020201)203:3<477::AID-MACP477>3.0.CO;2-M · DOI
- Bai, 2001, Macromol Chem Phys, 202, 1970, 10.1002/1521-3935(20010601)202:9<1970::AID-MACP1970>3.0.CO;2-Q · DOI
- Arita, 2004, e-Polymers, 003
- Uzulina, 2000, Macromol Symp, 150, 33, 10.1002/1521-3900(200002)150:1<33::AID-MASY33>3.0.CO;2-C · DOI
- Butte, 2001, DECHEMA Monograph, 137, 273
- Chong YK, Moad G, Rizzardo E, Skidmore MA, Thang SH. Macromolecules, in press.
- Cerreta, 1995, Bull Soc Chim Fr, 132, 67
- Rizzardo, 2001, Macromol Symp, 174, 209, 10.1002/1521-3900(200109)174:1<209::AID-MASY209>3.0.CO;2-O · DOI
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Block Copolymer Synthesis through the Use of Switchable RAFT Agents
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Metadata
- Authors
- Moad, G., Rizzardo, E., & Thang, S. H.
- Affiliations
- Commonwealth Scientific and Industrial Research Organisation (AU)
- Corresponding author
- Moad, Graeme
- Rizzardo, Ezio
- Thang, San H.
- Venue
- Polymer
- Publisher
- Elsevier BV
- Published
- 2008-03
- Volume
- 49
- Issue
- 5
- Pages
- 1079-1131
- ISSN
- 0032-3861 (ISSN-L)
- OpenAlex
- W2040062577
- Cited by
- 1,397
- References
- 528
- Citations by year
- 2026: 13 · 2025: 29 · 2024: 41 · 2023: 29 · 2022: 41 · 2021: 71 · 2020: 64 · 2019: 92 · 2018: 76 · 2017: 79 · 2016: 85 · 2015: 93 · 2014: 90 · 2013: 100 · 2012: 117
- FWCI
- 46.82
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Polymer (publishedVersion, cc-by-nc-nd)
- Funders
- Commonwealth Scientific and Industrial Research Organisation
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Physical Sciences › Chemistry › Organic Chemistry › Photopolymerization techniques and applications
- Keywords
- RAFT polymerization, RAFT agents, dithioesters, trithiocarbonates, dithiocarbamates, xanthates, controlled radical polymerization, block copolymers, star polymers, cyclopolymers, gradient copolymers, molecular weight control
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