Molecular Vibrations in the Exciton Theory for Molecular Aggregates. V. Electronic Spectra of Weakly-coupled Systems

Abstract

The theory of the gross vibrational structure in the electronic spectra of molecular aggregates is developed for the case of weak intermolecular interaction. The electronically excited states are represented by a set of m-m functions corrected to first order as described in Part IV of this series. An explicit treatment is given for aggregates with two molecules per unit cell. Formulae are obtained for the relative vibronic intensities, splittings, and polarization ratios in absorption spectra, and for relative quantum yields and polarization ratios in fluorescence spectra. The theoretical results are compared with those of the E-V coupling theory developed in Parts II and III. On the basis of this comparison, a general equation is put forward to relate the theoretical crystal splitting (i.e. the splitting for a rigid model) to observed polarization ratios in spectra. The theoretical results are compared with the observed vibrational structure in the 3800 Ǻ band system of anthracene crystal. The crystal splitting calculated from the observed polarization ratios is 380 cm^-1. The theory accounts, within the rather large experimental error, for the observed variations of polarization ratio in both the absorption and the fluorescence spectra of anthracene crystal.