SPECTROSCOPY OF CHLORINE MONOFLUORIDE ISOLATED IN RARE GAS MATRICES

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2000

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Ohio State University

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We report for the first time spectroscopy of chlorine monofluoride (ClF) isolated in rare gas matrices. The strongest absorption is to the dissociative $^{1}\Pi_{u}$ state around 275 nm. Upon laser excitation at 308 nm into this state we observe in emission a vibrational progression from 580 to 930 nm which can be safely attributed to $A^{\prime}\rightarrow X$ with $\omega_{e} = 780.7 cm^{-1}$ and $\omega_{e}x_{e} = 6.5 cm^{-1}$. The population accumulates in $A^{\prime}$ state with a phosphorescence lifetime of the order of one second. Excitation from $A^{\prime}$ to the ionic manifold results in two broad emission bands at 425 and 510 nm respectively. CIF is an interesting molecule in the perspective of condensed phase photochemistry. Upon excitation at 308 nm it dissociates with a quantum yield similar to the $F_{2}$ molecule. But as a heteronuclear molecule the two fragment atoms behave extremely differently: From experiments on matrix isolated $Cl_{2}$ in Kr and Ar it is known that cage exit of Cl atoms is negligible. In contrast, the fluorine up to unit probability with increasing excess energy. The negligible. In contrast, the fluorine atom leaves the cage with up to unit probability with increasing excess energy. The fragmented fluorine atoms and the parent molecules are recorded spectroscopically and the dissociation and recombination kinetics are analysed. The blue fluorescence bands after two-photon excitation are established as a channel for femtosecond pump-probe spectroscopy and time-resolved measurements of the dissociation in a condensed-phase environment are discussed.

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Author Institution: Institut f\""ur Experimentalphysik, Freie Universit\""ar Berlin

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