Abstract
Tetraisopropylthiuram disulfide dissociates reversibly in solution to form
dithiocarbamate thioradicals
which can be detected by e.s.r. (g 2.015). The thermodynamics of the dissociation has been examined
in decalin by quantitative e.s.r.
and a dissociation enthalpy of 104 � 2 kJ mol-1 and anentropy of dissociation of 57 � 5 JK-1 mol-1
has been obtained. Replacing the isopropyl group by other alkyl groups
significantly affects the extent of dissociation which decreases in the
sequence isopropyl ≈ cyclohexyl > ethyl ≈ methyl > benzyl as
the alkyl group is changed. Studies of the kinetics of dissociation of the thiuram disulfides are consistent with the e.s.r, observations and indicate that thio
radical recombination occurs at a near diffusion-controlled rate.
Cited by
23 articles.
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