Flash photolysis of intermediates in hydrated electron reactions
A triple flash photolysis apparatus is described. Hydrated electrons (e[sup - / sub aq]) produced by U.V. flash photolysis of some common inorganic anions (OH⁻, SO[sup = / sub 4]) were monitored at 633 nm. This species was identified by its absorption spectrum and by the effect of well known elec...
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ndltd-UBC-oai-circle.library.ubc.ca-2429-323132018-01-05T17:46:35Z Flash photolysis of intermediates in hydrated electron reactions Vidyarthi, Suinil Kumar A triple flash photolysis apparatus is described. Hydrated electrons (e[sup - / sub aq]) produced by U.V. flash photolysis of some common inorganic anions (OH⁻, SO[sup = / sub 4]) were monitored at 633 nm. This species was identified by its absorption spectrum and by the effect of well known electron scavengers. In the absence of an electron scavenger, e[sup - / sub aq] decayed largely by a second order process to form a comparatively long lived (τ~ms) intermediate, X. Results indicate that X is probably a dimeric hydrated electron (e[sup 2-/ sub 2])[sub aq] or a product therefrom and can be photodissociated in the 300 - 400 nm region to regenerate hydrated electrons. Metal ions Ag⁺ and Tl⁺ react with e[sup - / sub aq] to produce the respective short lived metal atoms (hyper-reduced states) which also regenerate e[sup - / sub aq] by a second flash. M⁰ + hν (λ~ 300 nm) → M⁺ + e[sup - / sub aq] Ag⁰ has an absorption spectrum with λ[sub max] at 315 nm and an oscillator strength of 0.63. This band is assigned as charge-transfer-to-solvent (CTTS). Acetone, which reacts rapidly with e[sup - / sub aq], produces a transient, presumably (CH₃)₂CO)⁻, at pH 11. The absorption spectrum of this transient was recorded, (λ[sub max] = 255 nm, ε[sub max] ≈ 1.3 x 10⁴ M⁻¹ cm⁻¹) and its photo-max max ^ lysis in this region was again shown to regenerate e[sup - / sub aq]. Hence, it seems that the absorption spectra of many such transients may be CTTS bands in that they produce e[sup - / sub aq] upon photolysis. The decay of e[sup - / sub aq] was followed in the presence of some inorganic gases, e.g., SF₆, N₂O and Xe. The possibility of intermediate formation in those reactions are discussed. The carbonate radical ion, CO[sup - / sub 3], was produced during the flash photolysis of an N₂O saturated alkaline (pH 11) solution containing CO₂ and was studied by its absorption spectrum and decay kinetics. It was demonstrated that HCOO⁻ ions, methanol or 2-propanol, commonly used OH scavengers, yield e[sup - / sub aq] upon flash photolysis. Science, Faculty of Chemistry, Department of Graduate 2011-03-10T19:36:34Z 2011-03-10T19:36:34Z 1973 Text Thesis/Dissertation http://hdl.handle.net/2429/32313 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. University of British Columbia |
collection |
NDLTD |
language |
English |
sources |
NDLTD |
description |
A triple flash photolysis apparatus is described. Hydrated
electrons (e[sup - / sub aq]) produced by U.V. flash photolysis of some common inorganic
anions (OH⁻, SO[sup = / sub 4]) were monitored at 633 nm. This species was identified by its absorption spectrum and by the effect of well known electron scavengers.
In the absence of an electron scavenger, e[sup - / sub aq] decayed largely
by a second order process to form a comparatively long lived (τ~ms)
intermediate, X. Results indicate that X is probably a dimeric hydrated electron (e[sup 2-/ sub 2])[sub aq] or a product therefrom and can be photodissociated in
the 300 - 400 nm region to regenerate hydrated electrons.
Metal ions Ag⁺ and Tl⁺ react with e[sup - / sub aq] to produce the respective
short lived metal atoms (hyper-reduced states) which also regenerate e[sup - / sub aq]
by a second flash.
M⁰ + hν (λ~ 300 nm) → M⁺ + e[sup - / sub aq]
Ag⁰ has an absorption spectrum with λ[sub max] at 315 nm and an oscillator strength of 0.63. This band is assigned as charge-transfer-to-solvent (CTTS).
Acetone, which reacts rapidly with e[sup - / sub aq], produces a transient,
presumably (CH₃)₂CO)⁻, at pH 11. The absorption spectrum of this transient
was recorded, (λ[sub max] = 255 nm, ε[sub max] ≈ 1.3 x 10⁴ M⁻¹ cm⁻¹) and its photo-max max ^
lysis in this region was again shown to regenerate e[sup - / sub aq].
Hence, it seems that the absorption spectra of many such transients may be CTTS bands in that they produce e[sup - / sub aq] upon photolysis.
The decay of e[sup - / sub aq] was followed in the presence of some inorganic gases, e.g., SF₆, N₂O and Xe. The possibility of intermediate formation in those reactions are discussed. The carbonate radical ion, CO[sup - / sub 3], was produced during the flash photolysis of an N₂O saturated alkaline (pH 11) solution containing CO₂ and was studied by its absorption spectrum and decay kinetics.
It was demonstrated that HCOO⁻ ions, methanol or 2-propanol, commonly used OH scavengers, yield e[sup - / sub aq] upon flash photolysis. === Science, Faculty of === Chemistry, Department of === Graduate |
author |
Vidyarthi, Suinil Kumar |
spellingShingle |
Vidyarthi, Suinil Kumar Flash photolysis of intermediates in hydrated electron reactions |
author_facet |
Vidyarthi, Suinil Kumar |
author_sort |
Vidyarthi, Suinil Kumar |
title |
Flash photolysis of intermediates in hydrated electron reactions |
title_short |
Flash photolysis of intermediates in hydrated electron reactions |
title_full |
Flash photolysis of intermediates in hydrated electron reactions |
title_fullStr |
Flash photolysis of intermediates in hydrated electron reactions |
title_full_unstemmed |
Flash photolysis of intermediates in hydrated electron reactions |
title_sort |
flash photolysis of intermediates in hydrated electron reactions |
publisher |
University of British Columbia |
publishDate |
2011 |
url |
http://hdl.handle.net/2429/32313 |
work_keys_str_mv |
AT vidyarthisuinilkumar flashphotolysisofintermediatesinhydratedelectronreactions |
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1718594711053139968 |