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 (3CT) 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 3NI* state. Then the slow secondary CS (125 ns) gives the long-lived 3CT 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 1NI*→1CT→3NI*→3CT. 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.
| Original language | English |
|---|---|
| Pages (from-to) | 11591-11599 |
| Number of pages | 9 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 59 |
| Issue number | 28 |
| DOIs | |
| State | Published - 6 Jul 2020 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
- charge transfer
- electron spin control
- intersystem crossing
- time-resolved EPR
- triplet state
ASJC Scopus subject areas
- Catalysis
- General Chemistry
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