Abstract
We obtained the resonant Raman scattering spectra of Zn‐phthalocyanine and of its fully deuterated analog, Zn‐phthalocyanine‐d16. We performed calculation of normal vibrations and using it, interpreted the Raman scattering spectra. We characterized the form of vibration with the aid of potential energy distribution. For the majority of vibrations the calculation adequately describes the observed isotropic shifts. The correspondence between the vibrational states of Zn‐phthalocyanine and metal complexes of tetrabenzoporphin has been established in confirmation of the proposed detailed interpretation of the spectra.
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