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      Cu(0)-RDRP of styrene: balancing initiator efficiency and dispersity

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          Abstract

          The optimisation of all components within Cu(0)-wire mediated polymerisation of styrene is illustrated yielding well-defined polystyrene with enhanced initiator efficiency and dispersity at higher molecular weights.

          Abstract

          Cu(0)-RDRP is a powerful technique to synthesise a wide range of polymeric materials and architectures with controlled molecular weight, low dispersities and high end group fidelity. The vast majority of reports using this technique focus on the polymerisation of acrylates or methacrylates, with very limited examples on styrene, which is surprising as this is one of the most important vinyl monomers. Herein we present the first Cu(0)-wire mediated polymerisation of styrene with enhanced initiator efficiency and dispersity. The structure of the ligand, the type of the initiator, the nature of the solvent and the catalyst concentration have been systematically varied to afford polystyrene at relatively high molecular weights (∼50 000 g mol −1) with excellent agreement between theoretical and experimental number average molecular weight values and good control over the molecular weight distributions ( Đ ∼ 1.15).

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          Most cited references54

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          Atom Transfer Radical Polymerization (ATRP): Current Status and Future Perspectives

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            Ultrafast synthesis of ultrahigh molar mass polymers by metal-catalyzed living radical polymerization of acrylates, methacrylates, and vinyl chloride mediated by SET at 25 degrees C.

            Conventional metal-catalyzed organic radical reactions and living radical polymerizations (LRP) performed in nonpolar solvents, including atom-transfer radical polymerization (ATRP), proceed by an inner-sphere electron-transfer mechanism. One catalytic system frequently used in these polymerizations is based on Cu(I)X species and N-containing ligands. Here, it is reported that polar solvents such as H(2)O, alcohols, dipolar aprotic solvents, ethylene and propylene carbonate, and ionic liquids instantaneously disproportionate Cu(I)X into Cu(0) and Cu(II)X(2) species in the presence of a diversity of N-containing ligands. This disproportionation facilitates an ultrafast LRP in which the free radicals are generated by the nascent and extremely reactive Cu(0) atomic species, while their deactivation is mediated by the nascent Cu(II)X(2) species. Both steps proceed by a low activation energy outer-sphere single-electron-transfer (SET) mechanism. The resulting SET-LRP process is activated by a catalytic amount of the electron-donor Cu(0), Cu(2)Se, Cu(2)Te, Cu(2)S, or Cu(2)O species, not by Cu(I)X. This process provides, at room temperature and below, an ultrafast synthesis of ultrahigh molecular weight polymers from functional monomers containing electron-withdrawing groups such as acrylates, methacrylates, and vinyl chloride, initiated with alkyl halides, sulfonyl halides, and N-halides.
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              Atom transfer radical addition and polymerization reactions catalyzed by ppm amounts of copper complexes.

              Over the past decade, copper-catalyzed atom transfer radical polymerization (ATRP) has had a tremendous impact on the synthesis of polymeric materials with well defined compositions, architectures and functionalities. Apart from synthetic aspects of ATRP, considerable effort has also been devoted to structural and mechanistic understanding of copper complexes involved in ATRP, as well as development of methodologies to decrease the amount of catalyst needed in these systems. This tutorial review reports on recent advances in the area of catalyst regeneration in ATRP and mechanistically similar atom transfer radical addition (ATRA) using environmentally benign reducing agents. The outlined processes termed ARGET (activators regenerated by electron transfer) and ICAR (initiators for continuous activator regeneration) ATRP enable the synthesis of well-defined (co)polymers and single addition adducts using very low concentrations of copper catalysts (1-100 ppm). Recent developments in this area could have profound industrial implications on the synthesis of well-defined polymeric materials and small organic molecules.
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                Author and article information

                Journal
                PCOHC2
                Polymer Chemistry
                Polym. Chem.
                Royal Society of Chemistry (RSC)
                1759-9954
                1759-9962
                August 28 2018
                2018
                : 9
                : 34
                : 4395-4403
                Affiliations
                [1 ]University of Warwick
                [2 ]Chemistry Department
                [3 ]Coventry
                [4 ]UK
                Article
                10.1039/C8PY00814K
                c106a43a-cd74-447d-9e45-5e2c14832087
                © 2018

                http://creativecommons.org/licenses/by/3.0/

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