Switchable antenna: a star-shaped ruthenium/osmium tetranuclear complex with azobis(bipyridine) bridging ligands |
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Authors: | Otsuki Joe Imai Arata Sato Katsuhiko Li Dong-Mei Hosoda Mayumi Owa Masao Akasaka Tetsuo Yoshikawa Isao Araki Koji Suenobu Tomoyoshi Fukuzumi Shunichi |
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Affiliation: | The College of Science and Technology, Nihon University, 1-8-14 Kanda Surugadai, Chiyoda-ku, Tokyo 101-8308, Japan. otsuki@chem.cst.nihon-u.ac.jp |
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Abstract: | A star-shaped Ru/Os tetranuclear complex, in which a central Os unit is linked to three peripheral Ru units by 4,4'-azobis(2,2'-bipyridine) (azobpy) bridging ligands, was prepared to examine the unique photodynamics regulated by its redox state. The Ru/Os tetranuclear complex exhibits Ru-based luminescence at 77 K, whereas the three-electron reduction (one for each azobpy) of the Ru/Os complex results in luminescence from the Os unit. The photoexcited state of the Ru/Os complex rapidly decays into low energy metal-to-ligand charge-transfer states, in which the excited electron is localized in the azobpy ligand in the form of azobpy(.-). Upon the one-electron reduction of the azobpy ligands, the above-mentioned low-energy states become unavailable to the photoexcited complex. As a result, an energy transfer from the Ru-based excited state to the Os-based excited state becomes possible. Ultrafast transient absorption measurements revealed that the energy transfer process consists of two steps; intramolecular electron transfer from the terminal bipyridine ligand (bpy(.-)) to form azobpy(2-) followed by a metal-to-metal electron transfer. Thus, the Ru/Os tetranuclear complex collects light energy into the central Os unit depending on the redox state of the bridging ligands, qualifying as a switchable antenna. |
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Keywords: | bridging ligands electron transfer photochemistry redox chemistry time‐resolved spectroscopy |
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