Ultrafast formation of I2 following 350-nm photodissociation of CF2I2 in n-hexane

This study presents the photodissociation dynamics of difluorodiiodomethane (CF2I2) in n-hexane by femtosecond pump-probe spectroscopy. Following 350-nm excitation of CF2I2 into the lowest-lying excited electronic state, the transient absorption spectra are measured between 355 and 785 nm up to a time delay of 1200 ps. The results suggest that electronically excited CF 2 I 2 ∗ molecules undergo a step-wise decay giving rise to two iodine fragments. The majority of the nascent iodine fragments combine on a 2-ps timescale to form molecular iodine. The spectral evolution is complete within 500 ps where the quantum yield of I2 formation is measured to be 32%.