ArticleJournal of the American Chemical Society2026
The Role of Chirality-Induced Spin Selectivity in Helicene-Based Photogenerated Radical Pairs.
Article in Journal of the American Chemical Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
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Authors and funding
10 authors.
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Abstract
Chirality-induced spin selectivity (CISS) revealed a close connection between molecular chirality and electron spin. Because CISS is observed even at room temperature, it offers a promising route toward spin-based technologies operable under ambient conditions. However, its microscopic origin remains the subject of debate. In recent theories, the parameters governing the electron motion through the chiral bridge play a key role in CISS efficiency. To disentangle this specific contribution from that arising from the overall intrinsic chirality of the molecule, we synthesized a new chiral donor-acceptor dyad (Dχ-B-A) incorporating a thia-bridged[4]helicene donor, known to have high CISS efficiency in transport experiments, and a perylene diimide (PDI) acceptor connected by a three-ethynylbenzene bridge. Transient absorption measurements at 85 K show that photoexcitation of PDI generates a long-lived radical pair (Dχ
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