Tunneling motion in (HCl)2 hydrogen-bonded dimer probed by electrostatic hexapole and doppler-selected TOF measurement for the internal energy distribution of [ClHCl]

Kohei Imura, H. Ohoyama, R. Naaman, D. C. Che, M. Hashinokuchi, T. Kasai

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

The tunneling motion in (HCl)2 hydrogen bonded dimer and its deuterate was probed by a 2 m long electrostatic hexapole field. The focusing curves of the dimers confirmed the existence of homo and heterodimers in the cluster beam. The homodimer, either H35Cl-H35Cl or H37Cl-H37Cl, undergoes a fast tunneling motion for the two hydrogen atoms in the dimer. The heterodimer, namely H35Cl-H37Cl, on the other hand, does not show such fast tunneling motion in the time scale of the experiment. The electric dipole moments for both (DCl)2 isotopomers were determined to be 1.5 ± 0.2 D, which is the same value for (HCl)2. The observed ratio of homo to heterodimer was estimated to be 30 ± 10, and this value differs largely from the natural abundance for the chlorine isotope. An experimental scheme to discern homo and heterodimers is proposed here. By looking at fragments in the (HCl)2 dimer photodissociation using a Doppler-selected time-of-flight (TOF) technique, internal energy distribution of the [ClHCl] fragment was measured in 121.6 nm photodissociation. The TOF spectrum consists of fast and slow velocity components for the dissociated H atoms. It is found that the slow H component that arises from the hydrogen escapes after many collisions. The fast H component that arises from the direct H escape without any collision, thus this component reflects an internal and/or electronic state of the counter part fragment, i.e. [ClHCl]. The vibrational structure of [ClHCl] was observed for the fast H component of the TOF spectrum. (C) 2000 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)137-145
Number of pages9
JournalJournal of Molecular Structure
Volume552
Issue number1-3
DOIs
Publication statusPublished - 2000 Sep 26
Externally publishedYes

Fingerprint

Static Electricity
internal energy
Dimers
Hydrogen
Electrostatics
energy distribution
dimers
electrostatics
Photodissociation
hydrogen
fragments
photodissociation
Chlorine
escape
Electric dipole moments
Isotopes
Atoms
Electronic states
collisions
electric moments

Keywords

  • Doppler-selected TOF
  • Electrostatic hexapole
  • Homo- and hetero-dimers
  • Hydrogen chloride dimer
  • Tunneling motion

ASJC Scopus subject areas

  • Structural Biology
  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Spectroscopy
  • Atomic and Molecular Physics, and Optics

Cite this

Tunneling motion in (HCl)2 hydrogen-bonded dimer probed by electrostatic hexapole and doppler-selected TOF measurement for the internal energy distribution of [ClHCl]. / Imura, Kohei; Ohoyama, H.; Naaman, R.; Che, D. C.; Hashinokuchi, M.; Kasai, T.

In: Journal of Molecular Structure, Vol. 552, No. 1-3, 26.09.2000, p. 137-145.

Research output: Contribution to journalArticle

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abstract = "The tunneling motion in (HCl)2 hydrogen bonded dimer and its deuterate was probed by a 2 m long electrostatic hexapole field. The focusing curves of the dimers confirmed the existence of homo and heterodimers in the cluster beam. The homodimer, either H35Cl-H35Cl or H37Cl-H37Cl, undergoes a fast tunneling motion for the two hydrogen atoms in the dimer. The heterodimer, namely H35Cl-H37Cl, on the other hand, does not show such fast tunneling motion in the time scale of the experiment. The electric dipole moments for both (DCl)2 isotopomers were determined to be 1.5 ± 0.2 D, which is the same value for (HCl)2. The observed ratio of homo to heterodimer was estimated to be 30 ± 10, and this value differs largely from the natural abundance for the chlorine isotope. An experimental scheme to discern homo and heterodimers is proposed here. By looking at fragments in the (HCl)2 dimer photodissociation using a Doppler-selected time-of-flight (TOF) technique, internal energy distribution of the [ClHCl] fragment was measured in 121.6 nm photodissociation. The TOF spectrum consists of fast and slow velocity components for the dissociated H atoms. It is found that the slow H component that arises from the hydrogen escapes after many collisions. The fast H component that arises from the direct H escape without any collision, thus this component reflects an internal and/or electronic state of the counter part fragment, i.e. [ClHCl]. The vibrational structure of [ClHCl] was observed for the fast H component of the TOF spectrum. (C) 2000 Elsevier Science B.V.",
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T1 - Tunneling motion in (HCl)2 hydrogen-bonded dimer probed by electrostatic hexapole and doppler-selected TOF measurement for the internal energy distribution of [ClHCl]

AU - Imura, Kohei

AU - Ohoyama, H.

AU - Naaman, R.

AU - Che, D. C.

AU - Hashinokuchi, M.

AU - Kasai, T.

PY - 2000/9/26

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N2 - The tunneling motion in (HCl)2 hydrogen bonded dimer and its deuterate was probed by a 2 m long electrostatic hexapole field. The focusing curves of the dimers confirmed the existence of homo and heterodimers in the cluster beam. The homodimer, either H35Cl-H35Cl or H37Cl-H37Cl, undergoes a fast tunneling motion for the two hydrogen atoms in the dimer. The heterodimer, namely H35Cl-H37Cl, on the other hand, does not show such fast tunneling motion in the time scale of the experiment. The electric dipole moments for both (DCl)2 isotopomers were determined to be 1.5 ± 0.2 D, which is the same value for (HCl)2. The observed ratio of homo to heterodimer was estimated to be 30 ± 10, and this value differs largely from the natural abundance for the chlorine isotope. An experimental scheme to discern homo and heterodimers is proposed here. By looking at fragments in the (HCl)2 dimer photodissociation using a Doppler-selected time-of-flight (TOF) technique, internal energy distribution of the [ClHCl] fragment was measured in 121.6 nm photodissociation. The TOF spectrum consists of fast and slow velocity components for the dissociated H atoms. It is found that the slow H component that arises from the hydrogen escapes after many collisions. The fast H component that arises from the direct H escape without any collision, thus this component reflects an internal and/or electronic state of the counter part fragment, i.e. [ClHCl]. The vibrational structure of [ClHCl] was observed for the fast H component of the TOF spectrum. (C) 2000 Elsevier Science B.V.

AB - The tunneling motion in (HCl)2 hydrogen bonded dimer and its deuterate was probed by a 2 m long electrostatic hexapole field. The focusing curves of the dimers confirmed the existence of homo and heterodimers in the cluster beam. The homodimer, either H35Cl-H35Cl or H37Cl-H37Cl, undergoes a fast tunneling motion for the two hydrogen atoms in the dimer. The heterodimer, namely H35Cl-H37Cl, on the other hand, does not show such fast tunneling motion in the time scale of the experiment. The electric dipole moments for both (DCl)2 isotopomers were determined to be 1.5 ± 0.2 D, which is the same value for (HCl)2. The observed ratio of homo to heterodimer was estimated to be 30 ± 10, and this value differs largely from the natural abundance for the chlorine isotope. An experimental scheme to discern homo and heterodimers is proposed here. By looking at fragments in the (HCl)2 dimer photodissociation using a Doppler-selected time-of-flight (TOF) technique, internal energy distribution of the [ClHCl] fragment was measured in 121.6 nm photodissociation. The TOF spectrum consists of fast and slow velocity components for the dissociated H atoms. It is found that the slow H component that arises from the hydrogen escapes after many collisions. The fast H component that arises from the direct H escape without any collision, thus this component reflects an internal and/or electronic state of the counter part fragment, i.e. [ClHCl]. The vibrational structure of [ClHCl] was observed for the fast H component of the TOF spectrum. (C) 2000 Elsevier Science B.V.

KW - Doppler-selected TOF

KW - Electrostatic hexapole

KW - Homo- and hetero-dimers

KW - Hydrogen chloride dimer

KW - Tunneling motion

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