Deciphering Charge Transfer Processes in Transition Metal Complexes from the Perspective of Ultrafast Electronic and Nuclear Motions

• Published in: The journal of physical chemistry letters 2024-05, Vol.15 (19), p.5250-5258
• Main Authors: Mara, Michael W., Weingartz, Nicholas P., Leshchev, Denis, Hsu, Darren, Valentine, Andrew, Mills, Alexis, Roy, Subhangi, Chakraborty, Arnab, Kim, Pyosang, Biasin, Elisa, Haldrup, Kristoffer, Kirschner, Matthew S., Rimmerman, Dolev, Chollet, Matthieu, Glownia, James M., van Driel, Timothy B., Castellano, Felix N., Li, Xiaosong, Chen, Lin X.
• Format: Article
• Language: English
• Subjects: Physical Insights into Light Interacting with Matter
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/acs.jpclett.4c00735

Chemical transformations in charge transfer states result from the interplay between electronic dynamics and nuclear reorganization along excited-state trajectories. Here, we investigate the ultrafast structural dynamics following photoinduced electron transfer from the metal–metal-to-ligand charge transfer state of an electron donor, a Pt dimer complex, to a covalently linked electron acceptor group using ultrafast time-resolved wide-angle X-ray scattering and optical transient absorption spectroscopy methods to disentangle the interdependence of the excited-state electronic and nuclear dynamics. Following photoexcitation, Pt–Pt bond formation and contraction takes up to 1 ps, much slower than the corresponding process in analogous complexes without electron acceptor groups. Because the Pt–Pt distance change is slow with respect to excited-state electron transfer, it can affect the rate of electron transfer. These results have potential impacts on controlling electron transfer rates via structural alterations to the electron donor group, tuning the charge transfer driving force.