Axle length effect on photoinduced electron transfer in triad rotaxane with porphyrin, [60]fullerene, and triphenylamine.

Photoinduced multiple electron-transfer processes of a newly synthesized rotaxane with one acceptor and two donors are studied with the time-resolved fluorescence and absorption methods. In this rotaxane, zinc porphyrin (ZnP) with a crown-ether necklace is employed as a photosensitized electron donor; through the crown-ether, a short axle with C(60) and triphenylamine (TPA) at both terminals is penetrating as an electron acceptor and a hole-shift, respectively (abbreviated as (ZnP;C(60)-(A(S))-TPA)(Rot)). The time-resolved fluorescence and transient absorption measurements reveal that the through-space electron-transfer processes take place via the excited states of the ZnP unit to the spatially arranged C(60) moiety, giving the radical ion pair (ZnP(*+);C(60)(*-)-(A(S))-TPA)(Rot) in polar solvents. Consecutively, (ZnP;C(60)(*-)-(A(S))-TPA(*+))(Rot) is also generated by the through-space hole-shift between ZnP and TPA, in addition to the through-bond charge separation via the excited state of the C(60) moiety. Both radial ion pairs have lifetimes of 320-420 ns, which are longer than those of the previously reported similar rotaxane with cationic longer axle (150-170 ns).