The rotationally resolved infrared (IR) spectrum of the He– complex has been measured in a cryogenic ion trap experiment at a nominal temperature of 4 K. Predissociation of the stored complex has been invoked by excitation of the degenerate ν2 mode of the sub-unit using a pulsed optical parametric oscillator system. An assignment of the experimental spectrum became possible through one-to-one correlations with bands of the spectrum theoretically predicted in Paper I [Harding et al., J. Chem. Phys. 156, 144307 (2022)]. 19 bands have been assigned and analyzed, and the energy term diagram of the lower states of this floppy molecular complex has been derived from combination differences (CDs) in the experimental spectrum. Ground state combination differences (GSCDs) reveal a large part of the energy term diagram for the He– complex in its vibrational ground state, v = 0. Experimental and theoretical term energies agree within experimental accuracy for the rotational fine structure associated with the total angular momentum quantum number J and the parity e/f as well as for the coarse spacing of the lowest K states of the complex. This favorable comparison shows that the potential energy surface (PES) calculated in Paper I is accurate. The barriers between the three equivalent global minima in this PES are relatively low and the He– complex is extremely floppy, with nearly unhindered internal rotation of the sub-unit. The resulting Coriolis interactions couple the internal and end-over-end rotation of the complex and contribute significantly to the energy terms. They are observed both in experiment and theory and are, e.g., the origin of different rotational constants for states of e and f parity. Also in this respect, experiment and theory agree very well. Despite the assignment and analysis of many bands of the extremely rich IR spectrum of He–, higher levels of excitation, including the complex stretching mode, need further attention.
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14 April 2022
Research Article|
April 13 2022
The He– complex. II. Infrared predissociation spectrum and energy term diagram
Thomas Salomon
;
Thomas Salomon
1
I. Physikalisches Institut, Universität zu Köln
, Zülpicher Str. 77, D-50937 Köln, Germany
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Stefan Brackertz
;
Stefan Brackertz
1
I. Physikalisches Institut, Universität zu Köln
, Zülpicher Str. 77, D-50937 Köln, Germany
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Oskar Asvany
;
Oskar Asvany
1
I. Physikalisches Institut, Universität zu Köln
, Zülpicher Str. 77, D-50937 Köln, Germany
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Igor Savić
;
Igor Savić
2
Department of Physics, Faculty of Sciences, University of Novi Sad
, Novi Sad, Serbia
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Dieter Gerlich
;
Dieter Gerlich
3
Department of Physics, Technische Universität Chemnitz
, D-09107 Chemnitz, Germany
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Michael E. Harding
;
Michael E. Harding
4
Institut für Nanotechnologie, Karlsruher Institut für Technologie (KIT), Campus Nord
, Postfach 3640, D-76021 Karlsruhe, Germany
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Filippo Lipparini
;
Filippo Lipparini
5
Dipartimento di Chimica e Chimica Industriale, Università di Pisa
, Via G. Moruzzi 13, I-56124 Pisa, Italy
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Jürgen Gauss
;
Jürgen Gauss
6
Department Chemie, Johannes Gutenberg-Universität Mainz
, Duesbergweg 10-14, D-55128 Mainz, Germany
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Ad van der Avoird
;
Ad van der Avoird
a)
7
Theoretical Chemistry, Institute for Molecules and Materials, Radboud University
, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands
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Stephan Schlemmer
Stephan Schlemmer
b)
1
I. Physikalisches Institut, Universität zu Köln
, Zülpicher Str. 77, D-50937 Köln, Germany
b)Author to whom correspondence should be addressed: schlemmer@ph1.uni-koeln.de
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b)Author to whom correspondence should be addressed: schlemmer@ph1.uni-koeln.de
J. Chem. Phys. 156, 144308 (2022)
Article history
Received:
February 05 2022
Accepted:
March 21 2022
Connected Content
This is a companion to:
The He– complex. I. Vibration-rotation-tunneling states and transition probabilities
Citation
Thomas Salomon, Stefan Brackertz, Oskar Asvany, Igor Savić, Dieter Gerlich, Michael E. Harding, Filippo Lipparini, Jürgen Gauss, Ad van der Avoird, Stephan Schlemmer; The He– complex. II. Infrared predissociation spectrum and energy term diagram. J. Chem. Phys. 14 April 2022; 156 (14): 144308. https://doi.org/10.1063/5.0087427
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