Two-photon excited deep-red and near-infrared emissive organic co-crystals

Two-photon excited deep-red and near-infrared emissive organic co-crystals
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DOI:
10.1038/s41467-020-18431-7
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发表时间:
2020-09
影响因子:
16.6
通讯作者:
Yu Wang;Huan-Bao Wu;Penghao Li;Su Chen;Leighton O. Jones;Martín A. Mosquera;Long Zhang;K. Cai-K.-Ca
Yu Wang;Huan-Bao Wu;Penghao Li;Su Chen;Leighton O. Jones;Martín A. Mosquera;Long Zhang;K. Cai-K.-Ca
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Yu Wang;Huan-Bao Wu;Penghao Li;Su Chen;Leighton O. Jones;Martín A. Mosquera;Long Zhang;K. Cai-K.-Ca

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Two-photon excited near-infrared fluorescence materials have garnered considerable attention because of their superior optical penetration, higher spatial resolution, and lower optical scattering compared with other optical materials. Herein, a convenient and efficient supramolecular approach is used to synthesize a two-photon excited near-infrared emissive co-crystalline material. A naphthalenediimide-based triangular macrocycle and coronene form selectively two co-crystals. The triangle-shaped co-crystal emits deep-red fluorescence, while the quadrangle-shaped co-crystal displays deep-red and near-infrared emission centered on 668 nm, which represents a 162 nm red-shift compared with its precursors. Benefiting from intermolecular charge transfer interactions, the two co-crystals possess higher calculated two-photon absorption cross-sections than those of their individual constituents. Their two-photon absorption bands reach into the NIR-II region of the electromagnetic spectrum. The quadrangle-shaped co-crystal constitutes a unique material that exhibits two-photon absorption and near-infrared emission simultaneously. This co-crystallization strategy holds considerable promise for the future design and synthesis of more advanced optical materials.