TY  - JOUR
A1  - Robinson, Matthew Scott
A1  - Niebuhr, Mario
A1  - Lever, Fabiano
A1  - Mayer, Dennis
A1  - Metje, Jan
A1  - Gühr, Markus
T1  - Ultrafast photo-ion probing of the ring-opening process in trans-stilbene oxide
JF  - Chemistry - a European journal
N2  - The ultrafast photo-induced ring opening of the oxirane derivative trans-stilbene oxide has been studied through the use of ultrafast UV/UV pump-probe spectroscopy by using photo-ion detection. Single- and multiphoton probe paths and final states were identified through comparisons between UV power studies and synchrotron-based vacuum ultraviolet (VUV) single-photon ionization studies. Three major time-dependent features of the parent ion (sub-450 fs decay, (1.5 +/- 0.2) ps, and >100 ps) were observed. These decays are discussed in conjunction with the primary ring-opening mechanism of stilbene oxide, which occurs through C-C dissociation in the oxirane ring. The appearance of fragments relating to the masses of dehydrogenated diphenylmethane (167 amu) and dehydrogenated methylbenzene (90 amu) were also investigated. The appearance of the 167 amu fragment could suggest an alternative ultrafast ring-opening pathway via the dissociation of one of the C-O bonds within the oxirane ring.
KW  - femtochemistry
KW  - mass spectrometry
KW  - photochemistry
KW  - small ring systems
KW  - stilbene oxide
Y1  - 2021
U6  - https://doi.org/10.1002/chem.202101343
SN  - 1521-3765
VL  - 27
IS  - 44
SP  - 11418
EP  - 11427
PB  - Wiley-VCH
CY  - Weinheim
ER  -