Polyisobutenes with a high content of terminal olefinic groups can be synthesized by using manganese(II) initiators in homogeneous solution. These easily accessible complexes initiate the polymerization at room temperature and above, and afford highly reactive, gel-free polyisobutenes with high viscosities. Furthermore, the initiators were successfully used for the copolymerization of isobutene with isoprene. The high activities of the Mn(II) initiators seem to be related to their weakly coordinating nitrile ligands, which are easily displaced by substrate molecules. Replacing the nitrile ligands by other more strongly coordinating ligands such as water reduces the initiator activity significantly. The Mn(II) initiators are surprisingly resistant to temperature.
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http://dx.doi.org/10.1002/chem.200400446 | DOI Listing |
Polymers (Basel)
January 2024
Graduate School of Advanced Science and Engineering, Hiroshima University, Kagamiyama 1-4-1, Higashihiroshima 739-8527, Japan.
Considering the sustainability of material development, coordination polymerization catalysts effective for 1,1-disubstituted olefins are receiving a great deal of attention because they can introduce a variety of plant-derived comonomers, such as β-pinene and limonene, into polyolefins. However, due to their sterically encumbered property, incorporating these monomers is difficult. Herein, we succeeded in the copolymerization of ethylene with various hydroxy- or siloxy-substituted vinylidenes using a fluorenylamido-ligated titanium catalyst-MMAO system.
View Article and Find Full Text PDFMacromol Rapid Commun
April 2021
Department of Macromolecular Science, Graduate School of Science, Osaka University, Toyonaka, Osaka, 560-0043, Japan.
tert-Butyl esters are demonstrated to function as chain transfer agents (CTAs) in the cationic copolymerization of vinyl ether (VE) and oxirane via concurrent vinyl-addition and ring-opening mechanisms. In the copolymerization of isopropyl VE and isobutylene oxide (IBO), the IBO-derived propagating species reacts with tert-butyl acetate to generate a copolymer chain with an acetoxy group at the ω-end. This reaction liberates a tert-butyl cation; hence, a polymer chain with a tert-butyl group at the α-end is subsequently generated.
View Article and Find Full Text PDFPolymers (Basel)
March 2020
A.V. Topchiev Institute of Petrochemical Synthesis RAS, 29 Leninsky Pr., Moscow 119991, Russia.
The free radical copolymerization of electron-acceptor and electron-donor vinyl monomers represents a particular case of sequence-controlled polymerization. The reactions of maleic anhydride (MA) or related compounds (acceptor comonomers) with α-olefins (donor comonomers) result in the formation of the alternating copolymers that have clear prospects for petrochemical and biomedical applications. However, in contrast to the well-established polymerization of acrylate monomers, these processes have not been studied theoretically using the density functional theory (DFT) calculations.
View Article and Find Full Text PDFPolymers (Basel)
January 2020
Beijing Key Lab of Special Elastomeric Composite Materials, Department of Materials Science and Engineering, Beijing Institute of Petrochemical Technology, Beijing 102617, China.
A random copolymer of isobutylene (IB) and 4-vinylbenzenecyclobutylene (4-VBCB) was synthesized by cationic polymerization at -80 °C using 2-chloro-2,4,4-trimethylpentane (TMPCl) as initiator. The laws of copolymerization were investigated by changing the feed quantities of 4-VBCB. The molecular weight of the copolymer decreased, and its molecular weight distribution (MWD) increased with increasing 4-VBCB content.
View Article and Find Full Text PDFCarbohydr Polym
September 2019
State Key Laboratory of Chemical Resource Engineering, College of Material Science and Engineering, Beijing University of Chemical Technology, 15 North 3th-Ring East Road, Chaoyang District, Beijing, 100029, PR China. Electronic address:
Sodium alginate (SA) is a marine-derived biocompatible polysaccharide with huge reserves and polyisobutylene (PIB) is a saturated elastomer with gas barrier property, bio-inertness, and biocompatibility. Herein, we developed the biomass-based ASA-g-(THF-b-PIB) graft copolymer/Ag (3-11 nm, 0.7-3.
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