Theoretical study on intramolecular hydroben transfer involving amino-substituted perylenequinone

摘要

2-Amino-perylenequinofle (2-NH2-PQ) and 3,l0-diamino-perylenequiflone (3.10-diNH2-PQ) were used as model compounds for investigating the intramolecular hydrogen transfer (IRTI reacitons tnvolvtng amino-substttuted per-ylenequinonoid photosensitizers (PQP). A semi-empirical MO method (AM Ii was employed to calculate the theor-etical values associated with the IHI process. It was found that amino-substitution enhanced the entropy of a specific isomer of PQ, causing it to be more stable than other possible isomers. Amino-substitution raised the HOMO energy levels (EHoMo) of PQ, hy increasing its electron-donating ability. It was also found that placing an NH~ group in the ?-position lowered the energy barriers to IHI in PQ in the ground state atsd the singlet excited state, and 3,l0-diNH’-substitution increased the IHI energy barriers in PQ in both states. The energy barrier for the double JUT was almost two times the energy barrier for the single IHT. making the double JUT a less important process. The IHT energy barrier for NH2-PQ decreased in the singlet excited state. while the energy barrier decrease from the excited state to ground state was larger for 2-NH2-PQ than for 3.t0-diNH’-PQ. The charge on the hydrogen atom and the molecular dipole moment varied during the IHI process. and the IHI energy barriers were governed by the differences in the charges on the hydrogen atom in the transition state and initial state. The dipole moment for the molecular singlet excited state changed considerably during the IHI process. indicting that IHI would he accelerated by strongly polar solvents. Like the PQ case, there was no correlation between changes in the charge on the hydrogen atom and dipole moment changes in the LHT process.