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

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 use...

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Published in:Nature communications 2020-09, Vol.11 (1), p.4633-4633, Article 4633
Main Authors: Wang, Yu, Wu, Huang, Li, Penghao, Chen, Su, Jones, Leighton O, Mosquera, Martín A, Zhang, Long, Cai, Kang, Chen, Hongliang, Chen, Xiao-Yang, Stern, Charlotte L, Wasielewski, Michael R, Ratner, Mark A, Schatz, George C, Stoddart, J Fraser
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Language:eng
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Summary: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.
ISSN:2041-1723
2041-1723