Research output: Contribution to journal › Article › peer-review
Efficient Spin Orbit Charge Transfer Intersystem Crossing and Slow Intramolecular Triplet-Triplet Energy Transfer in Bodipy-Perylenebisimide Compact Dyads and Triads. / Chen, Xi; Rehmat, Noreen; Kurganskii, Ivan V et al.
In: Chemistry - A European Journal, Vol. 29, No. 61, e202302137, 02.11.2023.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Efficient Spin Orbit Charge Transfer Intersystem Crossing and Slow Intramolecular Triplet-Triplet Energy Transfer in Bodipy-Perylenebisimide Compact Dyads and Triads
AU - Chen, Xi
AU - Rehmat, Noreen
AU - Kurganskii, Ivan V
AU - Maity, Partha
AU - Elmali, Ayhan
AU - Zhao, Jianzhang
AU - Karatay, Ahmet
AU - Mohammed, Omar F
AU - Fedin, Matvey V
N1 - Acknowledgements: J.Z. thanks the NSFC (U2001222), the Research and Innovation Team Project of Dalian University of Technology (DUT2022TB10), the Fundamental Research Funds for the Central Universities (DUT22LAB610) and the State Key Laboratory of FineChemicals for financial support. M. F. and I. K. thank the Ministry of Science and Higher Education of the Russian Federation (Grant No. 075-15-2020-779). © 2023 Wiley-VCH GmbH.
PY - 2023/11/2
Y1 - 2023/11/2
N2 - We prepared Bodipy (BDP)-perylenebisimide (PBI) donor-acceptor dyads/triad to study the spin orbit charge transfer intersystem crossing (SOCT-ISC). For BDP-PBI-3, in which BDP was attached at the imide position of PBI, higher singlet oxygen quantum yield (FD = 85%) was observed than the bay-substituted derivative BDP-PBI-1 (FD = 30%). Femtosecond transient absorption spectra indicate slow Förster resonance energy transfer (FRET; 40.4 ps) and charge separation (CS; 1.55 ns) in BDP-PBI-3, while for BDP-PBI-1, CS takes 2.8 ps. For triad BDP-PBI-2, ultrafast FRET (149 fs) and CS (4.7 ps) process were observed, the subsequent charge recombination (CR) takes 5.8 ns and long lived 3PBI* (179.8 µs) state is populated. Nanosecond transient absorption spectra of BDP-PBI-3 show that the CR gives upper triplet excited state (3BDP*) and subsequently, via a slow intramolecular triplet energy transfer (14.5 µs), the 3PBI* state is finally populated, indicating that upper triplet state is involved in SOCT-ISC. Time resolved electron paramagnetic resonance spectroscopy revealed that both radical pair ISC (RP ISC) and SOCT-ISC contribute to the ISC. A rare electron spin polarization of (e, e, e, e, e, e) was observed for the triplet state formed via the RP ISC mechanism, due to the S-T+1/T0 states mixing.
AB - We prepared Bodipy (BDP)-perylenebisimide (PBI) donor-acceptor dyads/triad to study the spin orbit charge transfer intersystem crossing (SOCT-ISC). For BDP-PBI-3, in which BDP was attached at the imide position of PBI, higher singlet oxygen quantum yield (FD = 85%) was observed than the bay-substituted derivative BDP-PBI-1 (FD = 30%). Femtosecond transient absorption spectra indicate slow Förster resonance energy transfer (FRET; 40.4 ps) and charge separation (CS; 1.55 ns) in BDP-PBI-3, while for BDP-PBI-1, CS takes 2.8 ps. For triad BDP-PBI-2, ultrafast FRET (149 fs) and CS (4.7 ps) process were observed, the subsequent charge recombination (CR) takes 5.8 ns and long lived 3PBI* (179.8 µs) state is populated. Nanosecond transient absorption spectra of BDP-PBI-3 show that the CR gives upper triplet excited state (3BDP*) and subsequently, via a slow intramolecular triplet energy transfer (14.5 µs), the 3PBI* state is finally populated, indicating that upper triplet state is involved in SOCT-ISC. Time resolved electron paramagnetic resonance spectroscopy revealed that both radical pair ISC (RP ISC) and SOCT-ISC contribute to the ISC. A rare electron spin polarization of (e, e, e, e, e, e) was observed for the triplet state formed via the RP ISC mechanism, due to the S-T+1/T0 states mixing.
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85172703667&origin=inward&txGid=9cf607ed67eb7bd0b2a7f4e735474446
UR - https://www.mendeley.com/catalogue/d8c66555-e0d7-3be1-83a4-e9674e58f554/
U2 - 10.1002/chem.202302137
DO - 10.1002/chem.202302137
M3 - Article
C2 - 37553294
VL - 29
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
SN - 0947-6539
IS - 61
M1 - e202302137
ER -
ID: 53739847