An Electron Spin Resonance Study of Some Reactions of Pentafluorosulfuranyl (SF5)

1975 ◽  
Vol 53 (16) ◽  
pp. 2361-2364 ◽  
Author(s):  
John Charles Tait ◽  
James Anthony Howard

A kinetic electron spin resonance study of the self-reaction of SF5 and a spectroscopic and kinetic e.s.r. study of the reaction of SF5 with 1,1-di-t-butylethylene are reported. This radical undergoes self-reaction by a second-order process and the rate constants are given by the Arrhenius equation log 2k1(M−1 s−1) = (10.3 ± 0.5) − (1.7 ± 0.5)/θ where θ = 2.303RT kcal mol−1. It adds to 1,1-di-t-butylethylene to give (t-Bu)2CCH2SF5 which decomposes by a first-order process with rate constants that obey the expression log k2(s−1) = (13 ± 0.4) − (10 ± 0.2)/θ. Both these rate constants are pertinent to kinetic studies of the photoinduced addition of SF5C1 to olefins.

1976 ◽  
Vol 54 (16) ◽  
pp. 2669-2675 ◽  
Author(s):  
James Anthony Howard ◽  
John Charles Tait

Trimethylgermylperoxy and triphenylgermylperoxy have been prepared and their kinetic behaviour investigated by electron spin resonance techniques. At low temperatures (< −50 °C) these radicals exist in equilibrium with the tetroxide. The thermodynamic parameters for this equilibrium (−ΔH0 ≈ 11.5 kcal mol−1 and −ΔS0 ≈ 26.5 cal deg−1 mol−1) are the same, within experimental error, for both radicals. Above −50 °C (CH3)3GeO2 and (C6H5)3GeO2 decay irreversibly by a unimolecular process. (C6H5)3GeO2 is slightly less stable than (CH3)3GeO2 although both radicals appear to fit an Arrhenius equation of the approximate form log (kepr1/s−1) ≈ 5 − 6/θ where θ = 2.303RT kcal mol−1.


1972 ◽  
Vol 50 (14) ◽  
pp. 2374-2377 ◽  
Author(s):  
J. A. Howard ◽  
J. E. Bennett

Absolute rate constants for the self-reaction of cyclopentylperoxy, cyclopentenylperoxy, and sec-butylperoxyradicals have been determined over a 125 °C temperature range. Arrhenius plots derived from these rate constants suggest that the mechanism for this reaction is more complex than the currently accepted Russell mechanism.


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