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Zero-kinetic-energy photoelectron spectroscopy from the ù Au state of acetylene: Renner–Teller interactions in the trans-bending vibration of C2H⁺2 X~²Πu

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.465888· OSTI ID:5922667
Double-resonance excitation via the ù Au state is used to record zero-kinetic-energy photoelectron spectra of acetylene. The analysis of these spectra leads to an improved value of 91 952±2cm⁻¹ for the adiabatic ionization potential to the C2H⁺2 X~²Πu ionic ground state. Because the ù Au intermediate state has a trans-bent geometry, transitions from it readily populate the trans-bending vibration of the ground state ion, leading to new information about this mode and its Renner--Teller interactions. The relative intensities of the Renner--Teller components and of the rotational structure within each component also provide information on the dynamics of the photoionization process.
Research Organization:
Argonne National Laboratory (ANL), Argonne, IL
Sponsoring Organization:
USDOE; Office of Health and Environmental Research (OHER)
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
5922667
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 9 Vol. 99; ISSN JCPSA6; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)
Country of Publication:
United States
Language:
English