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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

New polyphenylene-based macromolecular architectures by using well defined macromonomers synthesized via controlled polymerization methods

TL;DR: In this article, the authors describe recent directions in the preparation of PPP graft copolymers with various polymeric side-chains, including atom transfer radical polymerization or ring opening polymerization.
Journal ArticleDOI

Atom transfer radical copolymerization of n‐hexylmaleimide and styrene in an ionic liquid

TL;DR: In this article, the atom transfer radical copolymerization of N-hexylmaleimide and styrene in an ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate, was investigated.
Book ChapterDOI

Telechelic Oligomers and Macromonomers by Radical Techniques

TL;DR: In this paper, a review summarizes nearly 400 references (since 1990) intended to highlight directions on the synthesis of telechelic oligomers and macromonomers by radical techniques, taking into account the recent developments in conventional radical polymerizations, such as dead-end polymerizationand also telomerization reactions.
Journal ArticleDOI

Star polymers via atom transfer radical polymerization from adamantane-based cores

TL;DR: In this paper, a series of novel multifunctional initiators derived from adamantane-based derivatives were used in the syntheses of various styrenic and (meth)acrylic star polymers by atom transfer radical polymerization.
Journal ArticleDOI

Correlation of metal spin-state in alpha-diimine iron catalysts with polymerization mechanism

TL;DR: In this article, the α-diimine iron complexes with high-spin spin-state iron centers were found to polymerize styrene through a catalytic chain transfer (CCT) mechanism.
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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