Jump to Main Content
Dipole-Mediated Rectification of Intramolecular Photoinduced Charge Separation and Charge Recombination
- Bao, Duoduo, Upadhyayula, Srigokul, Larsen, Jillian M., Xia, Bing, Georgieva, Boriana, Nuñez, Vicente, Espinoza, Eli M., Hartman, Joshua D., Wurch, Michelle, Chang, Andy, Lin, Chung-Kuang, Larkin, Jason, Vasquez, Krystal, Beran, Gregory J. O., Vullev, Valentine I.
- Journal of the American Chemical Society 2014 v.136 no.37 pp. 12966-12973
- electric field, electron transfer, electronics, energy conversion, light, magnetic materials, molecular dynamics, nanotechnology
- Controlling charge transfer at a molecular scale is critical for efficient light harvesting, energy conversion, and nanoelectronics. Dipole-polarization electrets, the electrostatic analogue of magnets, provide a means for “steering” electron transduction via the local electric fields generated by their permanent electric dipoles. Here, we describe the first demonstration of the utility of anthranilamides, moieties with ordered dipoles, for controlling intramolecular charge transfer. Donor–acceptor dyads, each containing a single anthranilamide moiety, distinctly rectify both the forward photoinduced electron transfer and the subsequent charge recombination. Changes in the observed charge-transfer kinetics as a function of media polarity were consistent with the anticipated effects of the anthranilamide molecular dipoles on the rectification. The regioselectivity of electron transfer and the molecular dynamics of the dyads further modulated the observed kinetics, particularly for charge recombination. These findings reveal the underlying complexity of dipole-induced effects on electron transfer and demonstrate unexplored paradigms for molecular rectifiers.