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@ARTICLE{Nalin:465192,
author = {Nalin, Giammarco and Fehre, Kilian and Trinter, Florian and
Novikovskiy, Nikolay M. and Anders, Nils and Trabert, Daniel
and Grundmann, Sven and Kircher, Max and Khan, Arnab and
Tomar, Raghu and Hofmann, Max and Waitz, Markus and
Vela-Pérez, Isabel and Kastirke, Gregor and Siebert,
Juliane and Tsitsonis, Dimitrios and Fukuzawa, Hironobu and
Ueda, Kiyoshi and Williams, Joshua and Kargin, Denis and
Maurer, Martin and Kuestner-Wetekam, Catmarna and Marder,
Lutz and Viehmann, Johannes and Knie, Andre and Jahnke, Till
and Ilchen, Markus and Doerner, Reinhard and Pietschnig,
Rudolf and Demekhin, Philipp and Schoeffler, Markus},
title = {{P}hotoelectron circular dichroism of {O} 1s-photoelectrons
of uniaxially oriented trifluoromethyloxirane: energy
dependence and sensitivity to molecular configuration},
journal = {Physical chemistry, chemical physics},
volume = {23},
number = {32},
issn = {1463-9084},
address = {Cambridge},
publisher = {RSC Publ.},
reportid = {PUBDB-2021-03802, arXiv:2106.08071},
pages = {17248 - 17258},
year = {2021},
abstract = {The photoelectron circular dichroism (PECD) of the O
1s-photoelectrons of trifluoromethyloxirane (TFMOx) is
studied experimentally and theoretically for different
photoelectron kinetic energies. The experiments were
performed employing circularly polarized synchrotron
radiation and coincident electron and fragment ion detection
using cold target recoil ion momentum spectroscopy. The
corresponding calculations were performed by means of the
single center method within the relaxed-core Hartree–Fock
approximation. We concentrate on the energy dependence of
the differential PECD of uniaxially oriented TFMOx
molecules, which is accessible through the employed
coincident detection. We also compare the results for the
differential PECD of TFMOx to those obtained for the
equivalent fragmentation channel and similar photoelectron
kinetic energy of methyloxirane (MOx), studied in our
previous work. Thereby, we investigate the influence of the
substitution of the methyl group by the trifluoromethyl
group at the chiral center on the molecular chiral response.
Finally, the presently obtained angular distribution
parameters are compared to those available in the
literature.},
cin = {FS-PETRA-S / UFrankf. / DOOR ; HAS-User},
ddc = {540},
cid = {I:(DE-H253)FS-PETRA-S-20210408 /
$I:(DE-H253)UFrankf_-20120814$ /
I:(DE-H253)HAS-User-20120731},
pnm = {631 - Matter – Dynamics, Mechanisms and Control
(POF4-631) / 6G3 - PETRA III (DESY) (POF4-6G3)},
pid = {G:(DE-HGF)POF4-631 / G:(DE-HGF)POF4-6G3},
experiment = {EXP:(DE-H253)P-P04-20150101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34346440},
eprint = {2106.08071},
howpublished = {arXiv:2106.08071},
archivePrefix = {arXiv},
SLACcitation = {$\%\%CITATION$ = $arXiv:2106.08071;\%\%$},
UT = {WOS:000680882400001},
doi = {10.1039/D1CP02462K},
url = {https://bib-pubdb1.desy.de/record/465192},
}