sameAs
Terminology for reversible-deactivation radical polymerization previously called "controlled" radical or "living" radical polymerization (IUPAC Recommendations 2010)Advances in RAFT polymerization: the synthesis of polymers with defined end-groupsEnhancement of MHC-I antigen presentation via architectural control of pH-responsive, endosomolytic polymer nanoparticles.Rapid and systematic access to quasi-diblock copolymer libraries covering a comprehensive composition range by sequential RAFT polymerization in an Automated synthesizer.RAFT polymerization and some of its applications.Triple Activity of Lamivudine Releasing Sulfonated Polymers against HIV-1.Universal (switchable) RAFT agents.Synthesis of Discrete Oligomers by Sequential PET-RAFT Single-Unit Monomer Insertion.Toward living radical polymerization.Glossary of terms related to kinetics, thermodynamics, and mechanisms of polymerization (IUPAC Recommendations 2008)Definitions of terms relating to the structure and processing of sols, gels, networks, and inorganic-organic hybrid materials (IUPAC Recommendations 2007)Glossary of terms relating to thermal and thermomechanical properties of polymers (IUPAC Recommendations 2013)Living Free-Radical Polymerization by Reversible Addition−Fragmentation Chain Transfer: The RAFT ProcessAn arm-first approach to cleavable mikto-arm star polymers by RAFT polymerizationThiocarbonylthio end group removal from RAFT-synthesized polymers by a radical-induced processLiving polymerization: Rationale for uniform terminologyLiving free radical polymerization with reversible addition - fragmentation chain transfer (the life of RAFT)Tailored polymer architectures by reversible addition-frasmentation chain transferInitiating free radical polymerizationNon-Ionic, Poly(ethylene oxide)-Based Surfactants as Intercalants/Dispersants/Exfoliants for Poly(propylene)-Clay NanocompositesTailored polymers by free radical processesSynthesis of novel architectures by radical polymerization with reversible addition fragmentation chain transfer (RAFT polymerization)Novel Copolymers as Dispersants/Intercalants/Exfoliants for Polypropylene-Clay NanocompositesRAFT Polymerization: Adding to the PictureMechanism and kinetics of dithiobenzoate-mediated RAFT polymerization. I. The current situationRadical Addition–Fragmentation Chemistry and RAFT PolymerizationA simple method for determining protic end-groups of synthetic polymers by 1H NMR spectroscopyRAFT Agent Design and SynthesisApproaches to phthalimido and amino end-functional polystyrene by atom transfer radical polymerisation (ATRP)Multiarm organic compounds for use as reversible chain-transfer agents in living radical polymerizationsA novel synthesis of functional dithioesters, dithiocarbamates, xanthates and trithiocarbonatesFunctional polymers for optoelectronic applications by RAFT polymerizationMechanism and Kinetics of RAFT-Based Living Radical Polymerizations of Styrene and Methyl MethacrylateThiocarbonylthio Compounds [SC(Ph)S−R] in Free Radical Polymerization with Reversible Addition-Fragmentation Chain Transfer (RAFT Polymerization). Role of the Free-Radical Leaving Group (R)Thiocarbonylthio Compounds (SC(Z)S−R) in Free Radical Polymerization with Reversible Addition-Fragmentation Chain Transfer (RAFT Polymerization). Effect of the Activating Group ZLiving Free Radical Polymerization with Reversible Addition−Fragmentation Chain Transfer (RAFT Polymerization): Approaches to Star PolymersChain Transfer Activity of ω-Unsaturated Methacrylic Oligomers in Polymerizations of Methacrylic MonomersBinary Copolymerization with Catalytic Chain Transfer. A Method for Synthesizing Macromonomers Based on Monosubstituted MonomersThermolysis of RAFT-Synthesized Polymers. A Convenient Method for Trithiocarbonate Group EliminationSynthesis of Well-Defined Polystyrene with Primary Amine End Groups through the Use of Phthalimido-Functional RAFT Agents
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