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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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Synthesis, thermal properties, and specific interactions of high Tg increase in poly(2,6-dimethyl-1,4-phenylene oxide)-block-polystyrene copolymers

TL;DR: In this article, a block copolymers of poly(2,6-dimethyl-1,4-phenylene oxide) and polystyrene (PPO-b-PS copolymer) were synthesized by atom transfer radical polymerization.
Journal ArticleDOI

Thermal and mechanical characterization of poly(vinyl chloride)-b-poly(butyl acrylate)-b-poly(vinyl chloride) obtained by single electron transfer – degenerative chain transfer living radical polymerization in water

TL;DR: In this article, the synthesis of poly(vinyl chloride)-b-poly(n-butyl acrylate)-poly(poly( n)-butyl-acrylate-b-Poly(vinylon chloride) prepared by single electron transfer/degenerative chain transfer mediated living radical polymerization (SET-DTLRP) in a two-step process was reported.
Journal ArticleDOI

Alumina additives for fast iron-mediated AGET ATRP of MMA using onium salt as ligand

TL;DR: In this article, three kinds of alumina (acidic, neutral, and basic Al2O3) were used as additives for the control and rate enhancement of iron-mediated AGET (activators generated by electron transfer) ATRP (atom transfer radical polymerization) of methyl methacrylate (MMA) in the presence of limited amount of air.
Journal ArticleDOI

Chiral (–)‐DIOP Ruthenium Complexes for Asymmetric Radical Addition and Living Radical Polymerization Reactions

TL;DR: A series of ruthenium complexes with chiral phosphane ligands (Ru2Cl4[(−)-DIOP]3 (1), Ru(Ind)Cl[(-)DIOP) (2), and Ru(Cp*)Cl[ (−)- DIOP] (3), were synthesized, characterized by X-ray crystallography, and employed in asymmetric halogen transfer radical addition and metal-catalyzed living radical polymerization reactions of olefins, such as styrene, methyl acrylate (MA), and methyl methac
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Rate enhancement of nitroxyl radical-mediated polymerization

TL;DR: In this paper, an improved process for free radical polymerization is produced making it possible to control the growth steps of a polymerization to produce homopolymers and copolymers.
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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