Manipulating charge transfer excited state relaxation and spin crossover in iron coordination complexes with ligand substitution. Issue 1 (8th September 2016)

• Record Type: Journal Article
• Authors: Zhang, Wenkai; Kjær, Kasper S.; Alonso-Mori, Roberto; Bergmann, Uwe; Chollet, Matthieu; Fredin, Lisa A.; Hadt, Ryan G.; Hartsock, Robert W.; Harlang, Tobias; Kroll, Thomas; Kubiček, Katharina; Lemke, Henrik T.; Liang, Huiyang W.; Liu, Yizhu; Nielsen, Martin M.; Persson, Petter; Robinson, Joseph S.; Solomon, Edward I.; Sun, Zheng; Sokaras, Dimosthenis; van Driel, Tim B.; Weng, Tsu-Chien; Zhu, Diling; Wärnmark, Kenneth; Sundström, Villy; Gaffney, Kelly J.
• Is Part Of: Chemical science. Volume 8:Issue 1(2017)
• Page Start: 515
• Page End: 523
• Publication Date: 2016-09-08
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6sc03070j
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Optical and X-ray free-electron laser measurements reveal ligand substitution in an Fe(ii )-centered complex extends its MLCT lifetime. Abstract : Developing light-harvesting and photocatalytic molecules made with iron could provide a cost effective, scalable, and environmentally benign path for solar energy conversion. To date these developments have been limited by the sub-picosecond metal-to-ligand charge transfer (MLCT) electronic excited state lifetime of iron based complexes due to spin crossover – the extremely fast intersystem crossing and internal conversion to high spin metal-centered excited states. We revitalize a 30 year old synthetic strategy for extending the MLCT excited state lifetimes of iron complexes by making mixed ligand iron complexes with four cyanide (CN − ) ligands and one 2, 2′-bipyridine (bpy) ligand. This enables MLCT excited state and metal-centered excited state energies to be manipulated with partial independence and provides a path to suppressing spin crossover. We have combined X-ray Free-Electron Laser (XFEL) Kβ hard X-ray fluorescence spectroscopy with femtosecond time-resolved UV-visible absorption spectroscopy to characterize the electronic excited state dynamics initiated by MLCT excitation of [Fe(CN)4 (bpy)] 2− . The two experimental techniques are highly complementary; the time-resolved UV-visible measurement probes allowed electronic transitions between valence states making it sensitive to ligand-centered electronic states such as MLCT states, whereas the Kβ fluorescence spectroscopy provides a sensitive measure of changes in the Fe spin state characteristic of metal-centered excited states. We conclude that the MLCT excited state of [Fe(CN)4 (bpy)] 2− decays with roughly a 20 ps lifetime without undergoing spin crossover, exceeding the MLCT excited state lifetime of [Fe(2, 2′-bipyridine)3 ] 2+ by more than two orders of magnitude.