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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

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

Thermal degradation of two different polymers bearing amide pendant groups prepared by ATRP method

TL;DR: In this article, Piperidinocarbonylmethyl methacrylate (PyCMMA) and 1-(piperidino, carbonyl) ethylmethacryl (PyCEMA) monomers were synthesized using atom transfer radical polymerization.
Patent

A method for designing surfaces

TL;DR: In this article, a method of producing a binding surface for a target molecule having a functional binding site is proposed, which consists of identifying within the target molecule an anchor site which is remote from the functional binding sites, generating a pharmacophore model for the anchor site, and providing the anchor-site binding ligand on a surface of a substrate such that the ability of the anchor binding ligands to bind to the anchor sites is preserved.
Journal ArticleDOI

Atom transfer radical polymerization of styrene using a copper catalyst with a pseudohalogen anion

TL;DR: In this article, the authors reported the successful application of copper thiocyanate, a catalyst with a pseudohalide anion, in the presence of different ligands such as N,N,N=,N″, N‴,N‴-hexamethyltriethylenetetramine (HMTETA), pentyl-2-pyridylmethaneimine, and substituted bipyridine was found to be very efficient.
Journal ArticleDOI

Iron(II) complexes bearing anilido-imine ligands: Synthesis and catalysis on ATRP of methyl methacrylate

TL;DR: In this paper, the X-ray diffraction analysis reveals that 1a and 1b are dimeric complexes and 1c is hetero-binuclear complex. Complex 2c was confirmed to be a dimeric complex with the iron atom in a trigonal bipyramidal geometry.
Journal ArticleDOI

Poly(ethylene glycol) Block Copolymers by Atom Transfer Radical Polymerization‐Synthesis, Kinetics and Characterization

TL;DR: A series of block copolymers of poly(ethylene oxide) (PEO) with n-butyl methacrylate were prepared by atom transfer radical polymerization using varying number-average molecular weights of bifunctional PEO chloro macroinitiators and CuCl/HMTETA as a catalyst system at 85°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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