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- W4254145424 abstract "Iodinate anions are important in the chemistry of the atmosphere where they are implicated in ozone depletion and particle formation. The atmospheric chemistry of iodine is a complex overlay of neutral-neutral, ion-neutral and photochemical processes, where many of the reactions and intermediates remain poorly characterised. This study targets the visible spectroscopy and photostability of the gas-phase hypoiodite anion (IO−), the initial product of the I− + O3 reaction, by mass spectrometry equipped with resonance-enhanced photodissociation and total ion-loss action spectroscopies. It is shown that IO− undergoes photodissociation to I− + O (3P) over 637 – 459 nm (15700 – 21800 cm−1) due to excitation to the bound first singlet excited state. Electron photodetachment competes with photodissociation above the electron detachment threshold of IO− at 521 nm (19200 cm−1) with peaks corresponding to resonant autodetachment involving the singlet excited state and the ground state of neutral IO possibly mediated by a dipole-bound state." @default.
- W4254145424 created "2022-05-12" @default.
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- W4254145424 date "2021-09-01" @default.
- W4254145424 modified "2023-09-24" @default.
- W4254145424 title "Actinic Wavelength Action Spectroscopy of the IO− Reaction Intermediate" @default.
- W4254145424 doi "https://doi.org/10.26434/chemrxiv-2021-gztdd" @default.
- W4254145424 hasPublicationYear "2021" @default.
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