DNA hairpins having both a tethered
anthraquinone (Aq) end-capping
group and a perylenediimide (PDI) base surrogate were synthesized,
wherein Aq and PDI are each separated from a G-C base pair hole trap
by A-T and I-C base pairs (G = guanine, A = adenine, T= thymine, C
= cytosine, I = inosine). Selective photoexcitation of PDI at 532
nm generates a singlet radical ion pair (RP), <sup>1</sup>(G<sup>+•</sup>-PDI<sup>–•</sup>), while selective photoexcitation
of Aq at 355 nm generates the corresponding triplet RP, <sup>3</sup>(G<sup>+•</sup>-Aq<sup>–•</sup>). Subsequent
radical pair intersystem crossing within these spin-correlated RPs
leads to mixed spin states that exhibit spin-polarized, time-resolved
EPR spectra in which the singlet- and triplet-initiated RPs have opposite
phases. These results demonstrate that a carefully designed DNA hairpin
can serve as a photodriven molecular spin switch based on wavelength-selective
formation of the singlet or triplet RP without significant competition
from undesired energy transfer processes