The photochemical ring-opening of 1,3-cyclohexadiene imaged by ultrafast electron diffraction

• Published in: Nature chemistry 2019-06, Vol.11 (6), p.504-509
• Main Authors: Wolf, T. J. A., Sanchez, D. M., Yang, J., Parrish, R. M., Nunes, J. P. F., Centurion, M., Coffee, R., Cryan, J. P., Gühr, M., Hegazy, K., Kirrander, A., Li, R. K., Ruddock, J., Shen, X., Vecchione, T., Weathersby, S. P., Weber, P. M., Wilkin, K., Yong, H., Zheng, Q., Wang, X. J., Minitti, M. P., Martínez, T. J.
• Format: Article
• Language: English
• Subjects: 639/638/403; 639/638/439; 639/638/440; 639/638/563; Acceleration; Analytical Chemistry; Atmospheric chemistry; Biochemistry; Carbon; Chemical synthesis; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Electron diffraction; Electron states; Inorganic Chemistry; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Internal conversion; Organic Chemistry; Photochemicals; Physical Chemistry; Time dependence; Vitamin D
• ISSN: 1755-4330; 1755-4349
• DOI: 10.1038/s41557-019-0252-7

The ultrafast photoinduced ring-opening of 1,3-cyclohexadiene constitutes a textbook example of electrocyclic reactions in organic chemistry and a model for photobiological reactions in vitamin D synthesis. Although the relaxation from the photoexcited electronic state during the ring-opening has been investigated in numerous studies, the accompanying changes in atomic distance have not been resolved. Here we present a direct and unambiguous observation of the ring-opening reaction path on the femtosecond timescale and subångström length scale using megaelectronvolt ultrafast electron diffraction. We followed the carbon–carbon bond dissociation and the structural opening of the 1,3-cyclohexadiene ring by the direct measurement of time-dependent changes in the distribution of interatomic distances. We observed a substantial acceleration of the ring-opening motion after internal conversion to the ground state due to a steepening of the electronic potential gradient towards the product minima. The ring-opening motion transforms into rotation of the terminal ethylene groups in the photoproduct 1,3,5-hexatriene on the subpicosecond timescale. The photochemical electrocyclic ring-opening of 1,3-cyclohexadiene is a textbook organic chemistry reaction. Now, using ultrafast electron diffraction its reaction pathway has been resolved on the level of atomic distances and on its natural femtosecond timescale. Furthermore, coherent isomerization dynamics of the photoproduct 1,3,5-hexatriene were observed.