Abstract
The kinetics of the reaction of acid-base interaction of tetra(3-nitro-5-tert-butyl)phthalocyanine with cyclic and acyclic nitrogen-containing bases in benzene was studied. The process is found to proceed with a low rate. The schemes of acid-base interaction are proposed and the probable structure of the proton transfer complexes of tetra(3-nitro-5-tert-butyl)phthalocyanine are discussed. The effect of the nature of the nitrogencontaining base on the kinetic parameters of the process is revealed.
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