Global reaction pathways in the photodissociation of I3 - ions in solution at 267 and 400 nm studied by picosecond X-ray liquidography

Kyung Hwan Kim, Hosung Ki, Key Young Oang, Shunsuke Nozawa, Tokushi Sato, Joonghan Kim, Tae Kyu Kim, Jeongho Kim, Shin Ichi Adachi, Hyotcherl Ihee

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

The mechanism of a photochemical reaction involves the formation and dissociation of various short-lived species on ultrafast timescales and therefore its characterization requires detailed structural information on the transient species. By making use of a structurally sensitive X-ray probe, time-resolved X-ray liquidography (TRXL) can directly elucidate the structures of reacting molecules in the solution phase and thus determine the comprehensive reaction mechanism with high accuracy. In this work, by performing TRXL measurements at two different wavelengths (400 and 267 nm), the reaction mechanism of I3 - photolysis, which changes subtly depending on the excitation wavelength, is elucidated. Upon 400 nm photoexcitation, the I3 - ion dissociates into I 2 - and I. By contrast, upon 267 nm photoexcitation, the I3 - ion undergoes both two-body dissociation (I 2 -+I) and three-body dissociation (I-+2I) with 7:3 molar ratio. At both excitation wavelengths, all the transient species ultimately disappear in 80 ns by recombining to form the I3 - ion nongeminately. In addition to the reaction dynamics of solute species, the results reveal the transient structure of the solute/solvent cage and the changes in solvent density and temperature as a function of time. An eye for an I: By performing time-resolved X-ray liquidography measurements at two different excitation wavelengths, the wavelength dependence of the reaction mechanism of I3 - photodissociation is elucidated (see picture). In addition to the reaction dynamics of solute species, the results reveal the transient structure of the solute/solvent cage and the changes in solvent density and temperature as a function of time.

Original languageEnglish
Pages (from-to)3687-3697
Number of pages11
JournalChemPhysChem
Volume14
Issue number16
DOIs
Publication statusPublished - 2013 Nov 11

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Photodissociation
photodissociation
Ions
solutes
X rays
Wavelength
wavelengths
Photoexcitation
dissociation
ions
x rays
photoexcitation
excitation
Photochemical reactions
Photolysis
photochemical reactions
photolysis
Temperature
Molecules
temperature

All Science Journal Classification (ASJC) codes

  • Atomic and Molecular Physics, and Optics
  • Physical and Theoretical Chemistry

Cite this

Kim, Kyung Hwan ; Ki, Hosung ; Oang, Key Young ; Nozawa, Shunsuke ; Sato, Tokushi ; Kim, Joonghan ; Kim, Tae Kyu ; Kim, Jeongho ; Adachi, Shin Ichi ; Ihee, Hyotcherl. / Global reaction pathways in the photodissociation of I3 - ions in solution at 267 and 400 nm studied by picosecond X-ray liquidography. In: ChemPhysChem. 2013 ; Vol. 14, No. 16. pp. 3687-3697.
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abstract = "The mechanism of a photochemical reaction involves the formation and dissociation of various short-lived species on ultrafast timescales and therefore its characterization requires detailed structural information on the transient species. By making use of a structurally sensitive X-ray probe, time-resolved X-ray liquidography (TRXL) can directly elucidate the structures of reacting molecules in the solution phase and thus determine the comprehensive reaction mechanism with high accuracy. In this work, by performing TRXL measurements at two different wavelengths (400 and 267 nm), the reaction mechanism of I3 - photolysis, which changes subtly depending on the excitation wavelength, is elucidated. Upon 400 nm photoexcitation, the I3 - ion dissociates into I 2 - and I. By contrast, upon 267 nm photoexcitation, the I3 - ion undergoes both two-body dissociation (I 2 -+I) and three-body dissociation (I-+2I) with 7:3 molar ratio. At both excitation wavelengths, all the transient species ultimately disappear in 80 ns by recombining to form the I3 - ion nongeminately. In addition to the reaction dynamics of solute species, the results reveal the transient structure of the solute/solvent cage and the changes in solvent density and temperature as a function of time. An eye for an I: By performing time-resolved X-ray liquidography measurements at two different excitation wavelengths, the wavelength dependence of the reaction mechanism of I3 - photodissociation is elucidated (see picture). In addition to the reaction dynamics of solute species, the results reveal the transient structure of the solute/solvent cage and the changes in solvent density and temperature as a function of time.",
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Global reaction pathways in the photodissociation of I3 - ions in solution at 267 and 400 nm studied by picosecond X-ray liquidography. / Kim, Kyung Hwan; Ki, Hosung; Oang, Key Young; Nozawa, Shunsuke; Sato, Tokushi; Kim, Joonghan; Kim, Tae Kyu; Kim, Jeongho; Adachi, Shin Ichi; Ihee, Hyotcherl.

In: ChemPhysChem, Vol. 14, No. 16, 11.11.2013, p. 3687-3697.

Research output: Contribution to journalArticle

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AU - Kim, Kyung Hwan

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AU - Oang, Key Young

AU - Nozawa, Shunsuke

AU - Sato, Tokushi

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AU - Kim, Tae Kyu

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AU - Adachi, Shin Ichi

AU - Ihee, Hyotcherl

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