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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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Controlled/living radical polymerization: Features, developments, and perspectives

TL;DR: In this article, a review of recent mechanistic developments in the field of controlled/living radical polymerization (CRP) is presented, with particular emphasis on structure-reactivity correlations and "rules" for catalyst selection in ATRP, for chain transfer agent selection in reversible addition-fragmentation chain transfer (RAFT) polymerization, and for the selection of an appropriate mediating agent in stable free radical polymerisation (SFRP), including organic and transition metal persistent radicals.
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Platinum Group Organometallics Based on “Pincer” Complexes: Sensors, Switches, and Catalysts

TL;DR: This review discusses the synthetic methodologies that are currently available for the preparation of platinum group metal complexes containing pincer ligands and especially emphasizes different applications that have been realized in materials science such as the development and engineering of sensors, switches, and catalysts.
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Functional polymers by atom transfer radical polymerization

TL;DR: Atom transfer radical polymerization (ATRP) is one of the most successful methods to polymerize styrenes, (meth)acrylates and a variety of other monomers in a controlled fashion, yielding polymers with molecular weights predetermined by the ratio of the concentrations of consumed monomer to introduced initiator and with low polydispersities as discussed by the authors.
References
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Journal ArticleDOI

Polymerization of acrylates and methacrylates to make homopolmers and block copolymers initiated by N-alkoxyphthalimides and succinimides

TL;DR: In this article, various N-alkoxyphthalimides were prepared and tested as initiators for polymerization of a variety of monomers, and the reaction rates were sensitive to the choice of solvent.
Journal ArticleDOI

Studies in polymerization - XXIII. Initiation of polymerization by reaction between tetrakis (triphenyl phosphite)nickel(0) and balides: styrene

TL;DR: In this article, it was shown that the ligand exchange which occurs when tetrakis (triphenyl phosphite)nickel(0) (NiP 4 ) is dissolved in styrene (St) is the result of a rate-determining dissociation of NiP 4 followed by rapid complexing with the monomer to form NiP 3 (St).
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