Dimethoxyethane, activation energy

Figure 4. Arrhenius plot of the propagation constant, k , of sodium polystyryl polymerization in THF (lower curve) and in dimethoxyethane (upper curve). Note the negative activation energy (the lower curve) and the maximum in the upper curve...

Rate constant for the reaction of pyridinyl radical in acetonitrile divided by that for the reaction in 1,2-dimethoxyethane and the corresponding change in Gibbs activation energy. 

The upper temperature at which polyelectrolytes can be utilised can be extended by substitution of a polar organic solvent for water in the electrolyte. Conductivities of up to 1 Q 1m 1 have been obtained for sulphonated PEEK using anhydrous pyrazole and imidazole at 200 C (Kreuer et al., 1998). Solvents used to form electrolytes in Nafion membranes have included alcohols, amines, propylene carbonate, dimethoxyethane, dimethyl form-amide, dimethyl sulphoxide and TV-methyl pyrrolidone. Typical conductivities for the latter three solvents are 10 to 1 O-lm 1 at room temperature, and the conductivity is thermally activated with activation energies in the range 9 to 24 kJ/mol (Doyle et al., 2001). 

Examinations of other physical properties of pyridazine include the ESR spectrum of pyridazine radical anion (obtained with pyridazine and sodium or potassium in dimethoxyethane or tetra-hydrofuran, the self-diffusion coefficient and activation energy, the half-wave potential (-2.16V), and magnetic susceptibility. Pyridazine was reported not to fluoresce and no luminiscence could be observed even under very long exposures. More recently, room-temperature fluorescence in solution is reported to be at 23,800 cm (max.), with a life time of 2.6 x 10 . ... 

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