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  Synthesis of Nonsymmetric NBN-Embedded [6]- and [7]Helicenes with Amplified Activities

Jiao, Y., Sun, Z., Wang, Z., Fu, Y., & Zhang, F. (2023). Synthesis of Nonsymmetric NBN-Embedded [6]- and [7]Helicenes with Amplified Activities. Organic Letters, 25(48), 8766-8770. doi:10.1021/acs.orglett.3c03800.

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Jiao, Yang1, Author
Sun, Zuobang1, Author
Wang, Zhiheng1, Author
Fu, Yubin2, Author                 
Zhang, Fan1, Author
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1external, ou_persistent22              
2Department of Synthetic Materials and Functional Devices (SMFD), Max Planck Institute of Microstructure Physics, Max Planck Society, ou_3316580              

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 Abstract: Two C1-symmetric heterohelicenes were constructed by nonsymmetrically extending the ortho-fused structures of a C2v-symmetric NBN-embedded phenalene derivative and featured intense luminescence, large Stokes shifts, and successive reversible redox behaviors. Increasing one fused phenyl unit in such a helical structure led to a 10-fold-enhanced dissymmetry factor. Their strong double hydrogen-bond-donating capability makes them distinctly red-shifted in absorption, emission, and CD and CPL spectra upon the addition of fluoride anion.

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 Dates: 2023-11-222023-12-08
 Publication Status: Issued
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Title: Organic Letters
  Abbreviation : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 25 (48) Sequence Number: - Start / End Page: 8766 - 8770 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338