Die Makromolekulare Chemie · 1983 · 30 citations · 12 references
Natural SciencesChemistryChemical KineticsOrganic ChemistryPolymer ChemistryPolymer CharacterizationPolymer SynthesisPolymerization ChemistryPolymerization KineticsPolymerization ProcessesAnionic PolymerizationCopolymerization KineticsPolymerization Rate ConstantsPropagation ConstantPropagation KineticsRate ConstantsReactivityTermination Mechanisms
Abstract The absolute rate constants of propagation k p and of termination k t of ethyl α‐cyanoacrylate (ECNA) were determined in bulk at 30°C by means of the rotating sector method under conditions to suppress anionic polymerization; k p = 1 622 1 · mol −1 · s −1 and k t = 4,11 · 10 8 1 · mol −1 · s −1 for the polymerization in the presence of acetic acid, and k p = 1610 1 · mol −1 · s −1 and k t = 4,04 · 10 8 l · mol −1 · s −1 for the polymerization in the presence of 1,3‐propanesultone. The magnitude of k / k t determined was 6,39 · 10 −3 l · mol −1 · s −1 . The absolute rate constants for cross‐propagation in ECNA copolymerizations were also evaluated. Quantitative comparison of the rate constants with those of common monomers and polymer radicals shows that the strong electron‐withdrawing power of the ethoxycarbonyl and cyano groups enable the poly(ECNA) radical to add to monomers as fast as the other polymer radicals. The relatively high reactivity of ECNA, regardless of the type of attacking polymer radical, is interpreted by a transition state greatly stabilized by both the ethoxycarbonyl and the cyano groups.
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Vinylidene Cyanide. III<sup>1</sup>
Harry J. Gilbert, F. F. Miller, S. J. Averill et al. · Journal of the American Chemical Society · 1954 · 60 citations