1338236-79-5Relevant articles and documents
Hole tunneling and hopping in a Ru(bpy)32+- phenothiazine dyad with a bridge derived from oligo-p-phenylene
Walther, Mathieu E.,Wenger, Oliver S.
, p. 10901 - 10907 (2011/12/14)
A molecular dyad was synthesized in which a Ru(bpy)3 2+ (bpy = 2,2′-bipyridine) photosensitizer and a phenothiazine redox partner are bridged by a sequence of tetramethoxybenzene, p-dimethoxybenzene, and p-xylene units. Hole transfer from the oxidized metal complex to the phenothiazine was triggered using a flash-quench technique and investigated by transient absorption spectroscopy. Optical spectroscopic and electrochemical experiments performed on a suitable reference molecule in addition to the above-mentioned dyad lead to the conclusion that hole transfer from Ru(bpy)33+ to phenothiazine proceeds through a sequence of hopping and tunneling steps: Initial hole hopping from Ru(bpy) 33+ to the easily oxidizable tetramethoxybenzene unit is followed by tunneling through the barrier imposed by the p-dimethoxybenzene and p-xylene spacers. The overall charge transfer proceeds with a time constant of 41 ns, which compares favorably to a time constant of 1835 ns associated with equidistant hole tunneling between the same donor-acceptor couple bridged by three identical p-xylene units. The combined hopping/tunneling sequence thus leads to an acceleration of hole transfer by roughly a factor of 50 when compared to a pure tunneling mechanism.
