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The intermediate oxidation states are known, but, except for some compounds in the +3 and +4 states, they are not particularly important.
For some compounds, several protonation states were generated what increased the initial number of instances.
NMR experiments confirmed binding to the A-site for some compounds.
The 1H 1H and 1H 13C 2D NMR spectra for some compounds were also recorded.
Although, for some compounds a deviation from the correlation suggests that other transport mechanisms may coexist.
Rules are given for calculating the eight pure component parameters when volumetric data for some compounds are lacking or inaccurate.
For some compounds, good agreement has been observed between the experimentally observed amorphous solubility and the predicted value.
For some compounds, it may be necessary to apply correction factors to arrive at more accurate predicted logP values.
Moreover, for some compounds, oxidation of the C6 ethyl side chain to an unprecedented carboxylic acid was observed.
The tendency for TNI is to increase (going over 200∘C for some compounds) with increasing l.
Degradation curves were very reproducible for some compounds (benzene, toluene, o-xylene, o-dichlorobenzene and p-dichlorobenzene) and less reproducible for other (naphthalene and biphenyl).
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