000465192 001__ 465192 000465192 005__ 20250716150450.0 000465192 0247_ $$2doi$$a10.1039/D1CP02462K 000465192 0247_ $$2ISSN$$a1463-9076 000465192 0247_ $$2ISSN$$a1463-9084 000465192 0247_ $$2datacite_doi$$a10.3204/PUBDB-2021-03802 000465192 0247_ $$2altmetric$$aaltmetric:107699665 000465192 0247_ $$2pmid$$apmid:34346440 000465192 0247_ $$2arXiv$$aarXiv:2106.08071 000465192 0247_ $$2WOS$$aWOS:000680882400001 000465192 0247_ $$2openalex$$aopenalex:W3168402428 000465192 037__ $$aPUBDB-2021-03802 000465192 041__ $$aEnglish 000465192 082__ $$a540 000465192 088__ $$2arXiv$$aarXiv:2106.08071 000465192 1001_ $$0P:(DE-H253)PIP1087223$$aNalin, Giammarco$$b0$$eCorresponding author 000465192 245__ $$aPhotoelectron circular dichroism of O 1s-photoelectrons of uniaxially oriented trifluoromethyloxirane: energy dependence and sensitivity to molecular configuration 000465192 260__ $$aCambridge$$bRSC Publ.$$c2021 000465192 3367_ $$2DRIVER$$aarticle 000465192 3367_ $$2DataCite$$aOutput Types/Journal article 000465192 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1632386540_4155 000465192 3367_ $$2BibTeX$$aARTICLE 000465192 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000465192 3367_ $$00$$2EndNote$$aJournal Article 000465192 520__ $$aThe 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. 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