Long-lived photoinduced charge separation in adamantane-bridged donor-acceptor dyads: A case of adamantane bridge conferring orthogonal donor-acceptor orientation and restricted rotation

Design of compact donor -acceptor dyads that can exhibit charge separated (CS) state lifetimes extending to the microsecond time domain remains a major challenge even today. A simple but effective design strategy that can lead to long CS state lifetimes, in at least a few compact dyads, is still elusive. Herein we propose that use of adamantane (AD) as bridge can enhance CS state lifetimes in small molecule donor -acceptor dyads. This paper reports AD -bridged dyads, AN -AD -NB and PY-AD-NB, wherein the anthracene (or pyrene) donor and nitrobenzene acceptor are attached to bridgehead positions of AD. The singlet CS states generated upon irradiation were long-lived (lifetimes >1 mu s) and decayed to the ground and local triplet states, simultaneously. Electron transfer reactions of the CS state with secondary donor and acceptor established that the CS state is sufficiently long-lived to participate in intermolecular reactions. X-ray crystal structure of the AN -AD -NB dyad reveals that the donor and acceptor are orthogonally oriented, which reduces the donor -acceptor interaction, and thereby the charge recombination rate, significantly. By analysing the X-ray structure, we predict that all adamantane-bridged compact dyads will have orthogonal donor -acceptor orientation and exhibit long-lived CS states. We also report studies with bisadamantyl-substituted dyads and the results confirmed that the local triplets are formed from the CS state through hyperfine interaction. Based on our work we propose that the hyperfine interaction, which is not expected to occur in compact dyads because of the short donor -acceptor separation, can indeed occur if the CS state is sufficiently long-lived.