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Cited by 170

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Spin-Allowed Transitions Control the Formation of Triplet Excited States in Orthogonal Donor-Acceptor Dyads

Open access
Buck, Jason T., Boudreau, Andrew M., DeCarmine, André, Wilson, Reid W., Hampsey, James, Mani, Tomoyasu·2019·Chem

Abstract

Summary Triplet excited states (triplets) serve as key intermediates in critical technologies and processes ranging from organic synthesis to biomedicine to molecular electronics. Production of triplets of π-conjugated organic molecules without heavy atoms remains challenging. Spin-orbit, charge-transfer intersystem crossing (SOCT-ISC) directly converts singlet charge-separated states to triplets in an electron donor-acceptor (D-A) pair. Here, using a series of orthogonal D-A type boron dipyrromethene (BODIPY) derivatives as a model system, we show that the formation of triplets is largely controlled by the spin-allowed transitions rather than by SOCT-ISC. Yet, the SOCT-ISC process can still proceed much faster than ordinary ISC between (π, π*) states because the spin-orbit coupling of SOCT-ISC is 2 orders of magnitude stronger. We further show that such a process can produce triplets in a non-triplet-forming molecule, perylene. Our findings reveal a clear physical basis for this spin-forbidden process and provide guidelines for future molecular designs exploiting the process.

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Metadata

Authors
Buck, J. T., Boudreau, A. M., DeCarmine, A., Wilson, R. W., Hampsey, J., & Mani, T.
Venue
Chem
Publisher
Elsevier BV
Published
2019-01
Volume
5
Issue
1
Pages
138-155
ISSN
2451-9294 (ISSN-L)
OpenAlex
W2898401022
Cited by
170
References
2
FWCI
8.27
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Spin-Allowed Transitions Control the Formation of Triplet Excited States in Orthogonal Donor-Acceptor Dyads. https://app.cochat.ai/papers/10.1016/j.chempr.2018.10.001
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Buck, J. T., Boudreau, A. M., DeCarmine, A., Wilson, R. W., Hampsey, J., & Mani, T. (2019). Spin-Allowed Transitions Control the Formation of Triplet Excited States in Orthogonal Donor-Acceptor Dyads. Chem. https://doi.org/10.1016/j.chempr.2018.10.001

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