Journal of the American Chemical Society p. 1373 - 1379 (1987)
Update date:2022-09-26
Topics:
Nelsen, Stephen F.
Rumack, Daniel T.
Meot-Ner (Mautner), Michael
High pressure mass spectrometry was used to measure the kinetics for electron transfer between 54 pairs of tetraalkylhydrazines containing acyclic and f-ve- to seven-membered cyclic and bicyclic rings.Rate constants for electron transfer vary between 18 and 0.03 x 10-11 cm3molecule-1s-1 at 550 K.Variable-temeprature mesuremeants were made on five pairs over a 77-120 deg range.The (Me2N)2(1+), (EtMeN2)2 pair gave Ea=2.7 kcal/mol.The association energy for (Me2N)2 was measured at ΔH0=-13.0 kcal/mol near room temperature.These data are combined to estimate an energy separation of about 15.7 kcal/mol between associated (Me2N)2(1+)/(EtMeN)2 dimer complex and the transition state for electron transfer.The observed Bronsted α value of about 0.5 suggests a large barrier to electron transfer, and the kinetics suggests that the components largely retain their original structures in the associated complex, but that significant distortion is required to reach the transition-state geometry.The effect of alkyl group changes on the electron-transfer rate and comparison of these data with solution experiments are discussed.
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