Abstract
The acid-base interaction of octa(m-trifluoromethylphenyl)tetraazaporphin with nitrogen bases in benzene was studied. The rates of intermolecular transfer of sterically screened NH group protons from octa(m-trifluoromethylphenyl)tetraazaporphin to n-butylamine and tert-butylamine were found to be low. A scheme of the process was suggested. The influence of the nature of bases on the kinetic parameters of acid-base interactions was studied.
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