[go: up one dir, main page]

Pfeifer et al., 2010 - Google Patents

Tailor‐made soluble polymer supports: Synthesis of a series of ATRP initiators containing labile Wang linkers

Pfeifer 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 …
Continue reading at onlinelibrary.wiley.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • C08F8/32Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F293/00Macromolecular 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
    • C08F293/005Macromolecular 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2810/00Chemical modification of a polymer
    • C08F2810/20Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic 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
    • C07D207/30Heterocyclic 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
    • C07D207/34Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F290/00Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
    • C08F290/02Macromolecular 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
    • C08F290/04Polymers provided for in subclasses C08C or C08F
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/38Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C19/00Chemical modification of rubber
    • C08C19/30Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
    • C08C19/42Addition 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