Why and how could an aliphatic bridge allow for a longrange photoinduced charge separation in Tröger’s bases derivatives

PRISCILA A. LANZA; DIEGO DUSSO; MENA LEANDRO; ALEJANDRO PARISE; E. LAURA MOYANO; CARLOS A. CHESTA; D. MARIANO A. VERA

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY

ELSEVIER SCIENCE SA

Lugar: Amsterdam; Año: 2023

1010-6030

Tröger’s bases (TBs) have shown great potential to be used in different fields of science, such as biology, organic synthesis, photoelectronic applications, among others. As we have recently shown, a series of asymmetrically substituted Tröger’s base derivatives showed unexpected pullpush behavior. The aliphatic diazocine heterocycle which connect an electron donor and an electron acceptor moiety efficiently couples both electronic subsystems as if it were a typical π-conjugated linker. A thorough computational study was intended to shed light on the origin of the observed photophysical properties. A modified version of the CAM-B3LYP functional yielded an accurate prediction of the absorption and emission spectra of these species. In contrast, range-corrected and classical hybrid approaches showed too high and remarkably too low excited states energies, respectively. Unlike the typical π-linked donor/acceptor systems, a threshold was found in the redox gap of the centers in order to obtain a full charge separation. The role of the aliphatic bridge was found to be related to the unusual topology of the frontier orbitals involved, to the tension and particular molecular shape of the Tröger bicycle and to a contribution due to homoconjugation as well.Calculations on the actual Tröger derivatives and specific models were able to quantify the magnitude of the different contributions that make possible the charge separation.