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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

Synthesis of Well-Defined Allyl End-Functionalized Polystyrene by Atom Transfer Radical Polymerization with an Allyl Halide Initiator

TL;DR: Synthesis of Well-Defined Allyl End-Functionalized Polystyrene by Atom Transfer Radical Polymerization with an Allyl Halide Initiator.
Journal ArticleDOI

Controlling the degree of branching in vinyl polymerization

TL;DR: In this article, two different approaches, namely, Self-Condensing Vinyl Polymerization (SCVP) and Atom Transfer Radical Polymerisation (ATRP), were developed for controlling the degree of branching in vinyl systems, and a review article highlights recent advances in the science and technology in these two industrially very important approaches.
Journal ArticleDOI

Controlled Radical Polymerization of Styrene with Phosphoryl- and (Thiophosphoryl)dithioformates as RAFT Agents

TL;DR: In this paper, both thermally and AIBN-initiated RAFT styrene polymerizations were performed at different temperatures and the molar mass increased with time as expected for a controlled polymerization process.
Journal ArticleDOI

Synthesis and characterization of amphiphilic triblock polymers by copper mediated living radical polymerization

TL;DR: In this article, 2-Dimethylaminoethyl methacrylate (DMAEMA) and 2-diethylaminylmethacrylation (DEAEMA) block copolymers have been synthesized by using poly(ethylene glycol), poly(tetrahydrofuran) (PTHF) and poly (ethylene butylenes) macroinitiators with copper mediated living radical polymerization.
Journal ArticleDOI

“Living” Free Radical Ring-Opening Polymerization of 5,6-Benzo-2-methylene-1,3-dioxepane Using the Atom Transfer Radical Polymerization Method

TL;DR: In this paper, the polymerization of 5,6-benzo-2-methylene-1,3-dioxepane (BMDO) was carried out in the presence of ethyl α-bromobutyrate/CuBr/2,2‘-bipyridine.
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
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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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