TY - JOUR
T1 - Visualizing the three-dimensional arrangement of hydrogen atoms in organic molecules by Coulomb explosion imaging
AU - Green, Alice E
AU - Chen, Keyu
AU - Bhattacharyya, Surjendu
AU - Allum, Felix
AU - Usenko, Sergey
AU - Ashfold, Michael N R
AU - Baumann, Thomas M
AU - Borne, Kurtis D
AU - Brouard, Mark
AU - Burt, Michael
AU - Curchod, Basile F E
AU - Erk, Benjamin
AU - Forbes, Ruaridh J G
AU - Ibele, Lea M
AU - Ingle, Rebecca A
AU - Lam, Huynh Van Sa
AU - Li, Xiang
AU - Lin, Kang
AU - Mazza, Tommaso
AU - McManus, Joseph W
AU - Meyer, Michael
AU - Mullins, Terrence
AU - Nunes, Joao Pedro Figueira
AU - Rivas, Daniel
AU - Roerig, Aljoscha
AU - Rouzee, Arnaud
AU - Schmidt, Philipp
AU - Searles, John
AU - Senfftleben, Bjorn
AU - Stapelfeldt, Henrik
AU - Tanyag, Rico Mayro P
AU - Tranter, Florian
AU - Venkatachalam, Anbu Selvan
AU - Wang, Enliang
AU - Warne, Emily M
AU - Weber, Peter M
AU - Wolf, Thomas J A
AU - Jahnke, Till
AU - Rudenko, Artem
AU - Boll, Rebecca
AU - Rolles, Daniel
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/10/15
Y1 - 2025/10/15
N2 - Structure-sensitive methods based on femtosecond light or electron pulses are now making it possible to measure how molecular structures change during light-induced processes. Despite significant progress, high-fidelity imaging of nuclear positions remains a challenge even for relatively small molecular systems and, notably, regarding the positions of hydrogen atoms. As demonstrated in recent work, X-ray-induced Coulomb explosion imaging (CEI) may overcome this obstacle, as its sensitivity does not depend on the mass of the imaged atoms. The photoinduced ring opening of the heterocyclic molecule 2(5H)-thiophenone has attracted recent interest. Here, we show that CEI offers a powerful route to imaging the peripheral H atoms in this molecule and thus, more generally, to tracking detailed nuclear motions (e.g., isomerizations) in organic molecules on ultrafast time scales. Specifically, we record momentum-space Coulomb explosion images that report on the three-dimensional positioning of all nuclei within the molecule, for instance, distinguishing H atoms in C–H bonds that lie within or are directed out of the plane defined by the heavy atoms. The prospect of imaging peripheral H atoms to probe photochemical dynamics is explored by coupling ab initio molecular dynamics with classical Coulomb explosion simulations, thereby differentiating potential photoproduct isomers, including those whose structures primarily differ in the position of the hydrogens.
AB - Structure-sensitive methods based on femtosecond light or electron pulses are now making it possible to measure how molecular structures change during light-induced processes. Despite significant progress, high-fidelity imaging of nuclear positions remains a challenge even for relatively small molecular systems and, notably, regarding the positions of hydrogen atoms. As demonstrated in recent work, X-ray-induced Coulomb explosion imaging (CEI) may overcome this obstacle, as its sensitivity does not depend on the mass of the imaged atoms. The photoinduced ring opening of the heterocyclic molecule 2(5H)-thiophenone has attracted recent interest. Here, we show that CEI offers a powerful route to imaging the peripheral H atoms in this molecule and thus, more generally, to tracking detailed nuclear motions (e.g., isomerizations) in organic molecules on ultrafast time scales. Specifically, we record momentum-space Coulomb explosion images that report on the three-dimensional positioning of all nuclei within the molecule, for instance, distinguishing H atoms in C–H bonds that lie within or are directed out of the plane defined by the heavy atoms. The prospect of imaging peripheral H atoms to probe photochemical dynamics is explored by coupling ab initio molecular dynamics with classical Coulomb explosion simulations, thereby differentiating potential photoproduct isomers, including those whose structures primarily differ in the position of the hydrogens.
U2 - 10.1021/jacs.5c08730
DO - 10.1021/jacs.5c08730
M3 - Article (Academic Journal)
C2 - 41032373
SN - 0002-7863
VL - 147
SP - 37133−37143
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 41
ER -