Dire et al., 2007 - Google Patents
Nitroxide-mediated copolymerization of methacrylic acid and styrene to form amphiphilic diblock copolymersDire et al., 2007
- Document ID
- 1927831496883034567
- Author
- Dire C
- Charleux B
- Magnet S
- Couvreur L
- Publication year
- Publication venue
- Macromolecules
External Links
Snippet
The controlled free-radical polymerization of methacrylic acid was performed at 73 and 83° C using a methacrylic acid-based alkoxyamine and the nitroxide SG1 as a mediator in the presence of a small concentration of styrene, without protection of the carboxylic acid …
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene 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C=CC1=CC=CC=C1 0 title abstract description 208
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen
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- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides
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- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
- C08F2/06—Organic solvent
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/06—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
- C08F226/10—N-Vinyl-pyrrolidone
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- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/04—Polymers provided for in subclasses C08C or C08F
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Dire et al. | Nitroxide-mediated copolymerization of methacrylic acid and styrene to form amphiphilic diblock copolymers | |
Nicolas et al. | Living character of polymer chains prepared via nitroxide-mediated controlled free-radical polymerization of methyl methacrylate in the presence of a small amount of styrene at low temperature | |
Charleux et al. | Theoretical expression of the average activation− deactivation equilibrium constant in controlled/living free-radical copolymerization operating via reversible termination. Application to a strongly improved control in nitroxide-mediated polymerization of methyl methacrylate | |
Chauvin et al. | Nitroxide-mediated polymerization: the pivotal role of the kd value of the initiating alkoxyamine and the importance of the experimental conditions | |
Whitfield et al. | Universal conditions for the controlled polymerization of acrylates, methacrylates, and styrene via Cu (0)-RDRP | |
Guillaneuf et al. | First effective nitroxide-mediated polymerization of methyl methacrylate | |
Diaz et al. | Controlled polymerization of functional monomers and synthesis of block copolymers using a β-phosphonylated nitroxide | |
Dire et al. | Nitroxide-mediated controlled/living free-radical surfactant-free emulsion polymerization of methyl methacrylate using a poly (methacrylic acid)-based macroalkoxyamine initiator | |
Chaduc et al. | RAFT polymerization of methacrylic acid in water | |
Donovan et al. | RAFT polymerization of N, N-dimethylacrylamide in water | |
Luo et al. | Effect of reversible addition− fragmentation transfer (RAFT) reactions on (mini) emulsion polymerization kinetics and estimate of RAFT equilibrium constant | |
Zhang et al. | One-pot synthesis of poly (methacrylic acid-co-poly (ethylene oxide) methyl ether methacrylate)-b-polystyrene amphiphilic block copolymers and their self-assemblies in water via RAFT-mediated radical emulsion polymerization. A kinetic study | |
Lansalot et al. | RAFT miniemulsion polymerization: Influence of the structure of the RAFT agent | |
Lee et al. | Successful dispersion polymerization in supercritical CO2 using polyvinylalkylate hydrocarbon surfactants synthesized and anchored via RAFT | |
Kang et al. | Effect of complementary nucleobase interactions on the copolymer composition of RAFT copolymerizations | |
Darabi et al. | Nitroxide-mediated polymerization of 2-(diethylamino) ethyl methacrylate (DEAEMA) in water | |
Hoogenboom et al. | RAFT polymerization of 1-ethoxyethyl acrylate: a novel route toward near-monodisperse poly (acrylic acid) and derived block copolymer structures | |
Zhang et al. | Synthesis of Amphiphilic Poly (acrylic acid)-b-poly (n-butyl acrylate-co-acrylic acid) Block Copolymers with Various Microstructures via RAFT Polymerization in Water/Ethanol Heterogeneous Media | |
Nagelsdiek et al. | Synthesis of polymers containing cross-linkable groups by atom transfer radical polymerization: poly (allyl methacrylate) and copolymers of allyl methacrylate and styrene | |
Okubo et al. | Emulsifier-free, organotellurium-mediated living radical emulsion polymerization of butyl acrylate | |
Yu-Su et al. | Molecular imaging and analysis of branching topology in polyacrylates by atomic force microscopy | |
Pan et al. | Surfactant concentration effects on nitroxide-mediated living free radical miniemulsion polymerization of styrene | |
Simms et al. | Compartmentalization of reverse atom transfer radical polymerization in miniemulsion | |
Rikkou-Kalourkoti et al. | Synthesis, characterization and thermolysis of hyperbranched homo-and amphiphilic co-polymers prepared using an inimer bearing a thermolyzable acylal group | |
Rosselgong et al. | Core degradable star RAFT polymers: synthesis, polymerization, and degradation studies |