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Journal ArticleDOI

Controlled Radical Polymerization of Methacrylic Monomers in the Presence of a Bis(ortho-chelated) Arylnickel(II) Complex and Different Activated Alkyl Halides

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TLDR
In this article, a novel class of homogeneous nickel(II) catalysts, denoted as Ni(NCN)Br, is reported to mediate in the presence of activated alkyl halides, e.g., CCl4 or α-halocarbonyl compounds, and remarkably enough, poly(methyl methacrylate) (PMMA) with molecular weight up to at least 105 g/mol was synthesized in a controlled fashion.
Abstract
A novel class of homogeneous nickel(II) catalysts, i.e [Ni{o,o‘(CH2NMe2)2C6H3}Br], denoted as Ni(NCN‘)Br, is reported to mediate in the presence of activated alkyl halides, e.g., CCl4 or α-halocarbonyl compounds, a well-controlled radical polymerization of methacrylic monomers [methyl and n-butyl methacrylate), (MMA, n-BuMA)] at rather low temperatures (<100 °C). The number-average molecular weight of the polymer gradually increased with the monomer conversion and was inversely proportional to the initiator concentration of alkyl halides. The molecular weight distribution (MWD) remained very narrow during the whole course of the polymerization (MWD < 1.3). All the experimental data including a successful block copolymerization (n-BuMA-b-MMA) experiment were in agreement with a living polymerization process, and remarkably enough, poly(methyl methacrylate) (PMMA) with molecular weight up to at least 105 g/mol was synthesized in a controlled fashion. Increased thermal stability of the PMMA is a further indi...

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Journal ArticleDOI

Nickel-catalyzed supported ATRP of methyl methacrylate using cross-linked polystyrene triphenylphosphine as ligand

TL;DR: In this article, a supported catalytic system for methacrylate-based polymers is described, which consists of nickel(II) bromide immobilized onto a polystyrene resin carrying triphenylphosphine moieties (PS-PPh3/NiBr2).
Journal ArticleDOI

Thermal Stability of Functional P(S-r-MMA) Random Copolymers for Nanolithographic Applications

TL;DR: For both copolymers, the thermal treatment offsets the low-temperature monomer evolution while still maintaining surface characteristics suitable to induce the perpendicular orientation of the BCPs, thus ultimately extending the range of processing temperatures of theBCP film and consequently speeding the self-organization process.
Journal ArticleDOI

Nickel-mediated living radical polymerization of styrene in conjunction with tetraethylthiuram disulfide

Peng Li, +1 more
- 01 Jan 2002 - 
TL;DR: In this article, the reverse atom transfer radical polymerization (reverse ATRP) was used for the polymerization of styrene, and the results were shown to be in close agreement with those calculated by the assumption that one living radical generated one polymer chain, and molecular weight distributions were as low as 1.34.
Journal ArticleDOI

Controlled radical polymerization of styrene by quinone transfer radical polymerization (QTRP)

TL;DR: In this article, a quinone transfer radical polymerization (QTRP) was proposed for controlled chain polymerization of styrene at 100 °C in the presence of an ortho-quinone, e.g., phenanthrenequinone (PhQ).
Journal ArticleDOI

Grafting of poly(methyl methacrylate) or polyacrylonitrile onto polystyrene using ATRP technique

TL;DR: In this paper, a graft copolymerization was performed with methyl methacrylate (MMA) in toluene at 80°C and with acrylonitrile (AN) in tetrahydrofuran/ethyl- enecarbonate (62.5/37.5 v/v %) mixed solvent at 55°C.
References
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Journal ArticleDOI

Narrow molecular weight resins by a free-radical polymerization process

TL;DR: In this paper, free radical polymerization was used to obtain polystyrene and poly(styrene-co-butadiene) with narrow polydispersity (1.19-1.36) in the presence of 2,2,6, 6,6-tetramethyl-1-piperidinyloxy using benzoyl peroxide as initiator
Journal ArticleDOI

Controlled Living Radical Polymerization - Halogen Atom-Transfer Radical Polymerization Promoted by a Cu(I)Cu(II) Redox Process

TL;DR: An extension of ATRA to atom transfer radical addition, ATRP, provided a new and efficient way to conduct controlled/living radical polymerization as mentioned in this paper, using a simple alkyl halide, R-X (X = Cl and Br), as an initiator and a transition metal species complexed by suitable ligand(s), M t n /L x, e.g., CuX/2,2'-bipyridine, as a catalyst.
Journal ArticleDOI

|[lsquo]|Living|[rsquo]| Polymers

M. Szwarc
- 24 Nov 1956 - 
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