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Photoelectron circular dichroism in core level ionization of randomly oriented pure enantiomers of the chiral molecule camphor

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Hergenhahn,  Uwe
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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Rennie,  Emma E.
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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Kugeler,  Oliver
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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Marburger,  Simon
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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Lischke,  Toralf
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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引用

Hergenhahn, U., Rennie, E. E., Kugeler, O., Marburger, S., Lischke, T., Powis, I., & García, G. (2004). Photoelectron circular dichroism in core level ionization of randomly oriented pure enantiomers of the chiral molecule camphor. Journal of Chemical Physics, 120(10), 4553-4556. doi:10.1063/1.1651474.


引用: https://hdl.handle.net/11858/00-001M-0000-0011-0D3A-A
要旨
The inner-shell photoionization of unoriented camphor molecules by circularly polarized light has been investigated from threshold to a photoelectron kinetic energy of ~65 eV. Photoelectron spectra of the carbonyl C 1s orbital, recorded at the magic angle of 54.7° with respect to the light propagation direction, show an asymmetry of up to 6% on change of either the photon helicity or molecular enantiomer. These observations reveal a circular dichroism in the angle resolved emission with an asymmetry between forward and backward scattering (i.e., 0° and 180° to the light beam) which can exceed 12%. Since the initial state is an atomiclike spherically symmetric orbital, this strongly suggests that the asymmetry is caused by final-state effects dependent on the chiral geometry of the molecule. These findings are confirmed by electron multiple scattering calculations of the photoionization dynamics in the electric-dipole approximation.