The absorption cross sections of the gas-phase IO radical and the kinetics
and products of the IO self-reaction have been measured using the technique
of laser photolysis with time-resolved UV-vis absorption spectroscopy. The
IO absorption cross section at the peak of the (4,0) vibronic band of the
(A(2)Pi <-- X (2)Pi) transition at 427.2 nm, determined using the reaction
O(P-3) + CF3I to form IO and calibrated relative to the O-3 cross section w
as found to be (1.9 +/- 0.17) x 10(-17) cm(2)molecule(-1) at 295 K and 1.13
nm fwhm spectral resolution. The IO cross sections were found to exhibit a
negative temperature dependence. The kinetics of the IO self-reaction were
measured using the reaction IO(P-3) + I-2 to form IO, and the self-reactio
n rate coefficient k(1), determined from the loss of IO radicals in the abs
ence of ozone, was found to be (8.2 +/- 1.3) x 10(-11) molecules(-1) cm(3)
s(-1) at 295 K and 760 Torr. The self-reaction rate coefficient was found t
o be independent of pressure between 100 and 760 Torr, and to display a neg
ative temperature dependence between 222 and 325 K. described by k(1) = (4.
1 +/- 3.4) x 10(-11) exp{(220 +/- 230)/T} molecules(-1) cm(3) s(-1). All er
rors are 2 sigma. Four potential product channels exist for the IO self-rea
ction: IO + IO --> 2I + O-2 (1a), IO + IO --> I-2 + O-2 (1b), IO + IO --> O
IO + I (1c), IO + IO + M --> I2O2 + M (1d). No direct measurement of I atom
production was performed. I-2 formation was observed, but attributed to IO
-catalyzed I atom recombination (I + IO + M --> I2O + M; I + I2O --> I-2 IO). OIO formation was observed and shown to result from the IO self-reacti
on. Formation of a broadband absorbing product underlying the IO absorption
at low (lambda < 400 nm) wavelengths was observed, and tentatively attribu
ted to I2O2. The OIO cross sections and yield from the IO + IO reaction wer
e determined via measurement of OIO production from the IO + BrO reaction w
hich allowed limits to be placed on the branching ratio for OIO formation i
n the IO self-reaction at 295 K and 760 Torr. Branching ratios for all reac
tion channels were found to lie in the ranges 0.07 less than or equal to k(
1a)/k(1) less than or equal to 0.15, k(1b)/k(1) less than or equal to 0.05,
0.30 less than or equal to k(1c)/k(1) less than or equal to 0.46, and 0.42
less than or equal to k(1d)/k(1) less than or equal to 0.55 at 295 K and 7
60 Torr. The results are compared with previous studies of the IO self-reac
tion, and their implications for atmospheric iodine chemistry are considere
d.