2006
DOI: 10.1002/aoc.1045
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Polymerization of methyl methacrylate using bis(β‐ketoamino)nickel(II)–MAO catalytic systems

Abstract: The polymerization of methyl methacrylate (MMA) was investigated using a series of bis(β-ketoamino)nickel(II) complexes in combination with methylaluminoxane in toluene solution. The binary catalyst is necessary for initiating MMA polymerization and producing PMMA with high molecular weights but broad molecular weight distributions. The effects of reaction temperature and Al : Ni molar ratios on the polymerization of MMA were examined in detail. Both steric bulk and electronic effects of the substituents aroun… Show more

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Cited by 29 publications
(16 citation statements)
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“…As depicted in Figure 1, the crystal structures of the complex Ni{CF 3 C(O)CHC[N(naphthyl)]CH 3 } 2 were similar to those of the analogue complexes we previously reported, 21,22 and all shared the fourcoordination binding mode around a nickel(II) center.…”
Section: Structure Analysessupporting
confidence: 78%
“…As depicted in Figure 1, the crystal structures of the complex Ni{CF 3 C(O)CHC[N(naphthyl)]CH 3 } 2 were similar to those of the analogue complexes we previously reported, 21,22 and all shared the fourcoordination binding mode around a nickel(II) center.…”
Section: Structure Analysessupporting
confidence: 78%
“…The CAN stretching mode in P(MMA-co-DMPA) has been observed at about 1180 cm À1 and the S-H stretching of P(MMA-co-AM) samples at about 2560 cm À1 . NMR spectra confirmed the formation of the co-polymers, and the resonance of aliphatic protons allowed to assess the random atactic linkage between monomers [36]. GPC traces allowed to determine the molecular weights of the samples, in the range 5 Â 10 4 -5 Â 10 3 a.m.u., depending on the different effects of monomers with different polarity.…”
Section: Resultsmentioning
confidence: 96%
“…Nickel (II) complexes bearing N, O-chelate ligand activation for MMA polymerization yielded poly (methyl methacrylate) (PMMA) with rich syndiotacticity microstructure [4][5][6][7][8][9][10]. The chelating polymers find applications in bioinorganic industry [11], wastewater treatment [12,13], pollution control [14], hydrometallurgy [15], preconcentration [16], anionic polyelectrolyte hydrogels [17], cation-exchange resins [18] , showed potential applications in material science as conductive [19], luminescent [20], magnetic, porous, chiral or non-linear optical materials [21], catalytic [22][23][24][25],organic synthesis [26], polymer drug graft, recovery of trace metal ions [13] and antimicrobial activities [27,28].…”
Section: Introductionmentioning
confidence: 99%