Abstract
A very broad and flat shape of the log kcs vs. - Δ Gcs relation for the intermolecular electron transfer (ET) in the fluorescence quenching reaction in contrast to the bell-shaped log kCR vs. - Δ GCR relation of produced 1LIP's (loose ion pairs) are discussed, leading to the mechanisms of the D, A distance distribution and formation of multiple IP states with different structures depending on the D, A interaction strength, solvation and - Δ G for ET. The solvent dependent structures and multiple states mechanisms derived here agree with the conclusions derived from the studies on exciplex phenomena as discussed in Part 2 and their roles of crucial importance in organic photochemical reactions are demonstrated.