| Literature DB >> 32270586 |
Dongyi Liu1, Ahmed M El-Zohry2, Maria Taddei3, Clemens Matt4, Laura Bussotti3, Zhijia Wang1, Jianzhang Zhao1, Omar F Mohammed2, Mariangela Di Donato3,5, Stefan Weber4.
Abstract
We prepared conceptually novel, fully rigid, spiro compact electron donor (Rhodamine B, lactam form, RB)/acceptor (naphthalimide; NI) orthogonal dyad to attain the long-lived triplet charge-transfer (3 CT) state, based on the electron spin control using spin-orbit charge transfer intersystem crossing (SOCT-ISC). Transient absorption (TA) spectra indicate the first charge separation (CS) takes place within 2.5 ps, subsequent SOCT-ISC takes 8 ns to produce the 3 NI* state. Then the slow secondary CS (125 ns) gives the long-lived 3 CT state (0.94 μs in deaerated n-hexane) with high energy level (ca. 2.12 eV). The cascade photophysical processes of the dyad upon photoexcitation are summarized as 1 NI*→1 CT→3 NI*→3 CT. With time-resolved electron paramagnetic resonance (TREPR) spectra, an EEEAAA electron-spin polarization pattern was observed for the naphthalimide-localized triplet state. Our spiro compact dyad structure and the electron spin-control approach is different to previous methods for which invoking transition-metal coordination or chromophores with intrinsic ISC ability is mandatory.Entities:
Keywords: charge transfer; electron spin control; intersystem crossing; time-resolved EPR; triplet state
Year: 2020 PMID: 32270586 DOI: 10.1002/anie.202003560
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336