منابع مشابه
Reactivity ratios, and mechanistic insight for anionic ring-opening copolymerization of epoxides.
Reactivity ratios were evaluated for anionic ring-opening copolymerizations of ethylene oxide (EO) with either allyl glycidyl ether (AGE) or ethylene glycol vinyl glycidyl ether (EGVGE) using a benzyl alkoxide initiator. The chemical shift for the benzylic protons of the initiator, as measured by (1)H NMR spectroscopy, were observed to be sensitive to the sequence of the first two monomers adde...
متن کاملUCST behavior of polyampholytes based on stoichiometric RAFT copolymerization of cationic and anionic monomers.
Polyampholytes with controlled equimolar ratio of charges were synthesized by reversible addition-fragmentation chain transfer (RAFT) copolymerization of cationic and anionic monomers. The resulting charge-neutral polyampholytes exhibit upper critical solution temperature (UCST) thermoresponsive behavior in ethanol-water and methanol-water solvent mixtures based on electrostatic attraction. Fin...
متن کاملHalf-Titanocenes Containing Anionic Ancillary Donor Ligands: Effective Catalyst Precursors for Ethylene/Styrene Copolymerization
This review summarizes recent results for ethylene/styrene copolymerization using half-titanocenes containing anionic donor ligands, Cp’TiX2(Y) (X = halogen, alkyl; Y = aryloxo, ketimide etc.)–cocatalyst systems. The product composition, the styrene incorporation and microstructures in the resultant copolymers are highly influenced by the anionic donor employed. A methodology for an exclusive s...
متن کاملCopolymerization Using Lipase Catalyst
Enzymatic ring-opening copolymerization of lactones was carried out by using Pseudomonas f luorescens lipase in bulk. In the copolymerizaton of r-caprolactone (E-CL) and b-valerolactone at 60°C for 10 days a copolymer with molecular weight of 3.7 x 103 was obtained and its structure was found to be of random structure having both units from 13C NMR anlaysis. Effects of the feed ratio, the react...
متن کاملSequence selection during copolymerization.
We analyze a simple model for the copolymerization of two chemically distinct monomers that displays a wide variety of product sequence compositions depending on the rate coefficients for the stepwise addition of each monomer to a growing polymer chain. We show that in certain regions of parameter space the copolymer sequence composition depends sensitively on these parameter values, and we com...
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ژورنال
عنوان ژورنال: The Journal of the Society of Chemical Industry, Japan
سال: 1966
ISSN: 0023-2734,2185-0860
DOI: 10.1246/nikkashi1898.69.2_317