Pfeifer et al., 2010 - Google Patents
Tailor‐made soluble polymer supports: Synthesis of a series of ATRP initiators containing labile Wang linkersPfeifer et al., 2010
- Document ID
- 9019087210694362597
- Author
- Pfeifer S
- Lutz J
- Publication year
- Publication venue
- Macromolecular Chemistry and Physics
External Links
Snippet
A series of functional initiators for atom transfer radical polymerization (ATRP) was prepared. These structures contain an ATRP initiating site, a labile p‐alkoxybenzyl ester Wang linker and a functional end‐group (ie, COOH, N3, OH, C CH, or NHFmoc). These novel …
- 229920000642 polymer 0 title abstract description 45
Classifications
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
-
- 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
- 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
-
- 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
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with heteroatoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- 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
- 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
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Pfeifer et al. | Development of a library of N‐substituted maleimides for the local functionalization of linear polymer chains | |
Glassner et al. | Diels–Alder reactions as an efficient route to high purity cyclic polymers | |
Opsteen et al. | Modular synthesis of ABC type block copolymers by “click” chemistry | |
Koo et al. | Limitations of radical thiol‐ene reactions for polymer–polymer conjugation | |
Lutz et al. | Combining atom transfer radical polymerization and click chemistry: a versatile method for the preparation of end‐functional polymers | |
Hardy et al. | Side‐chain ferrocene‐containing (meth) acrylate polymers: Synthesis and properties | |
Shi et al. | Tadpole‐shaped amphiphilic copolymers prepared via RAFT polymerization and click reaction | |
Durmaz et al. | Preparation of ABC miktoarm star terpolymer containing poly (ethylene glycol), polystyrene, and poly (tert‐butylacrylate) arms by combining Diels–Alder reaction, atom transfer radical, and stable free radical polymerization routes | |
Durmaz et al. | Preparation of block copolymers via Diels Alder reaction of maleimide‐and anthracene‐end functionalized polymers | |
Altintas et al. | ABC‐type hetero‐arm star terpolymers through “click” chemistry | |
Kakuchi et al. | Controlled Positioning of Activated Ester Moieties on Well‐Defined Linear Polymer Chains | |
Hong et al. | Controlled polymerization of acrylic acid under 60Co irradiation in the presence of dibenzyl trithiocarbonate | |
Fu et al. | One‐pot synthesis of heterograft copolymers via “graft onto” by atom transfer nitroxide radical coupling chemistry | |
Hilf et al. | A “click” approach to ROMP block copolymers | |
Hong et al. | Dendrimer‐star polymer and block copolymer prepared by reversible addition‐fragmentation chain transfer (RAFT) polymerization with dendritic chain transfer agent | |
Chen et al. | Synthesis of poly (vinyl acetate) with fluorescence via a combination of RAFT/MADIX and “click” chemistry | |
Wiltshire et al. | Degradable star polymers with high “click” functionality | |
Nishimori et al. | Design of maleimide monomer for higher level of alternating sequence in radical copolymerization with styrene | |
Pfeifer et al. | Tailor‐made soluble polymer supports: Synthesis of a series of ATRP initiators containing labile Wang linkers | |
Duxbury et al. | Glaser coupling of polymers: Side‐reaction in Huisgens “click” coupling reaction and opportunity for polymers with focal diacetylene units in combination with ATRP | |
Baysak et al. | Synthesis and post-polymerization modification of polyester containing pendant thiolactone units | |
McLeod et al. | Well‐defined epoxide‐containing styrenic polymers and their functionalization with alcohols | |
Tong et al. | Synthesis of well‐defined azide‐terminated poly (vinyl alcohol) and their subsequent modification via click chemistry | |
Choi et al. | Influence of residual impurities on ring‐opening metathesis polymerization after copper (I)‐catalyzed alkyne‐azide cycloaddition click reaction | |
Zhen et al. | Atom transfer radical polymerization of solketal acrylate using cyclohexanone as the solvent |