Abstract
The kinetics of acid-base interaction between tetra(3-nitro-5-tert-butyl)phthalocyanine and cyclic and acyclic nitrogen bases in benzene was studied. The reaction was found to occur with a low rate. The structure and reactivity of protolytes were shown to be interrelated. The structure and stability of the proton-transfer complexes formed are considered.
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Original Russian Text © O.A. Petrov, A.V. Glazunov, 2006, published in Zhurnal Fizicheskoi Khimii, 2006, Vol. 80, No. 9, pp. 1597–1602.
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Petrov, O.A., Glazunov, A.V. Kinetic characteristics of intermolecular proton transfer from NH groups of tetra(3-nitro-5-tert-butyl)phthalocyanine in nitrogen base-benzene systems. Russ. J. Phys. Chem. 80, 1411–1416 (2006). https://doi.org/10.1134/S0036024406090093
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DOI: https://doi.org/10.1134/S0036024406090093