An optically generated transient absorbing state in the polymethine pyrylium dyes EK 9860 and 9740 is described. The broadband absorption is produced when solutions of the dyes are irradiated by a 1060 nm picosecond duration pulse. The absorbing state spans the wavelength range from ∼520 to ≳800 nm and is characterized by a molar extinction coefficient of ∼1×104 and by a decay time as short as 13.4 psec (in 9860). The latter result and the 7 psec value previously reported for the recovery of ground state absorption at 1060 nm following excitation at the same wavelength are accommodated by a three level relaxation mechanism. This approach treats the visible absorption as arising from electronic transitions both from the first excited singlet state and from a transient intermediate level. Lack of structure in the transient visible absorption indicates that the transition populates high density bound state manifolds or continuum states.
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Olson et al. (1978) studied this question.
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