Abstract
The state of octaphenyltetrapyrazinoporphyrazine in dimethylsulfoxide was studied. The proton transfer complex formed was found to be fairly stable; its structure was suggested. The complex was kinetically unstable in strongly basic media. The influence of the nature of cyclic and acyclic nitrogen bases on the rate and activation parameters of the destruction of the proton transfer octaphenyltetrapyrazinoporphyrazine complex was studied.
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