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Charge reorganization energies (k) of inter-ring carbon-carbon (IRCC) bond connected conjugated polycyclics are shown to exhibit an electric-field-driven anisotropic character. An external electric field parallel to the IRCC linker(s) reduces k while the field vertical to the molecular plane does the opposite. This anisotropic character can be modulated by introducing inter-ring noncovalent locks into appropriate sites.
Danick Briand, Silvia Demuru, Xi Chen, Brince Paul Kunnel, Jaemin Kim
Giovanni Boero, Andras Kis, Jürgen Brugger, Georg Fantner, Nicola Marzari, Norma Rivano, Zhenyu Wang, Xia Liu, Ana Conde Rubio, Berke Erbas, Mitali Banerjee, Jin Jiang, Marcos Penedo Garcia
Philippe Schwaller, Junwu Chen