Femtosecond transient absorption anisotropy studies have been performed for two porphycenes of different symmetry. In 2,7,12,17-tetraphenylporphycene, the chemical identity of two trans forms implies a change in the S₀–S₁ transition-moment direction upon tautomerization. Exploiting this phenomenon, the rates of double hydrogen transfer in both the S₀ and S₁ states (1.4×10¹² s^−1 and 2.7×10¹¹ s^−1, respectively) have been determined by performing time-resolved anisotropy studies. In the asymmetric 9-amino-2,7,12,17-tetraphenylporphycene, tautomerization occurs with a similar rate in the ground state. In the S₁ state, the reaction is hindered in its vibrationally relaxed form, but the excitation spectra suggest that it may occur for an unrelaxed molecule. Unlike all porphycenes that have been studied so far, 9-amino-2,7,12,17-tetraphenylporphycene does not reveal significant changes in anisotropy owing to intramolecular double hydrogen transfer; rather, the transition-moment directions are similar in the two tautomeric forms. Analysis of the molecular orbitals allows for an explanation of the “lockingâ€� of the transition moments: it is due to a large splitting of the two HOMO orbitals, which retain the order of their energies in the two tautomers.