Generation of phosphorescent triplet states via photoinduced electron transfer: Energy and electron transfer dynamics in pt porphyrin-rhodamine b dyads

摘要

Control over generation and dynamics of excited electronic states is fundamental to their utilization in all areas of technology. We present the first example of multichromophoric systems in which emissive triplet states are generated via a pathway involving photoinduced electron transfer (ET), as opposed to local intrachromophoric processes. In model dyads, PtP-Ph _n-pRhB ~+ (1-3, n = 1-3), comprising platinum(II) meso-tetraarylporphyrin (PtP) and Rhodamine B piperazine derivative (pRhB ~+), linked by oligo-p-phenylene bridges (Ph _n), upon selective excitation of pRhB ~+ at a frequency below that of the lowest allowed transition of PtP, room-temperature T _1→S _0 phosphorescence of PtP was observed. The pathway leading to the emissive PtP triplet state includes excitation of pRhB ~+, ET with formation of the singlet radical pair, intersystem crossing within that pair, and subsequent radical recombination. Because of the close proximity of the triplet energy levels of PtP and pRhB ~+, reversible triplet-triplet (TT) energy transfer between these states was observed in dyads 1 and 2. As a result, the phosphorescence of PtP was extended in time by the long decay of the pRhB ~+ triplet. Observation of ET and TT in the same series of molecules enabled direct comparison of the distance attenuation factors ? between these two closely related processes.