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Updated: Jul 5, 2026

Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development
Published on: April 15, 2013
A host-induced intramolecular charge-transfer complex and light-driven radical cation formation of a molecular triad
Dapeng Zou1, Samir Andersson, Rong Zhang
1School of Chemical Science and Engineering, Department of Chemistry, Organic Chemistry, Royal Institute of Technology (KTH), Stockholm, Sweden.
Abstract:
The host-guest chemistry of systems containing a molecular triad Ru(bpy) 3-MV (2+)-naphthol complex (denoted as Ru (2+)-MV (2+)-Np, 1) and cucurbit[8]uril (CB[8]) is investigated by NMR, ESI-MS, UV-vis, and electrochemistry. The Ru (2+)-MV (2+)-Np guest and CB[8] host can form a stable 1:1 inclusion complex, in which the naphthalene residue is back-folded and inserted together with the viologen residue into the cavity of CB[8]. The selective binding of Ru (2+)-MV (2+)-Np guest with beta-CD and CB[8] host is also investigated. We find that CB[8] binds the Ru (2+)-MV (2+)-Np guest stronger than beta-CD. Upon light irradiation, a MV (+*) radical cation stabilized in the cavity of CB[8] accompanied by the naphthalene residue has been observed. This novel system may open a new way for design and synthesis of photoactive molecular devices.
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