Photochromic processes of a new class of spiroindoline compounds (subs
tituted 6-benzoyl-3,5-diaryl-spiro[cyclohexa-2,4-diene- 1,2'-indolines
]) have been investigated by stationary irradiation and by laser flash
photolysis. Ring-opening and ring-closure are reversible, but with re
peated irradiation concentration of dye decreases. In laser flash phot
olysis experiments a strong solvent dependence was found. Ring-opening
competes with intersystem crossing to T-1 and is the only reaction pa
thway in nonpolar solvents such as cyclohexane. Values of Phi .epsilon
have been measured and are found to be strongly dependent on excitati
on wavelength for merocyanine formation.