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    Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/101133


    Title: Synthesis and two-photon properties of multi-branched fluorophores composed of ladder-type conjugated cores and functionalized diquinoxalinylamino peripheries
    Authors: 林子超;Lin, Tzu-Chau;Li, Mei-Ling;Liu, Che-Yu;Tsai, Ming-Yu;Lee, Ying-Hsuan;Febriani, Yuyun;Lin, Ja-Hon;Shen, Yu-Kai
    Contributors: 理學院化學學系
    Keywords: Fluorescence;Fluorophores;Lasers;Photonics;Two-photon absorption
    Date: 2014-03-01
    Issue Date: 2026-04-21 14:25:09 (UTC+8)
    Publisher: Wiley-VCH Verlag;Weinheim: WILEY-VCH Verlag
    Abstract: 摘要: Two multipolar fluorophores using ladder‐type oligo‐(p‐phenylene) units as the central π‐bridges and functionalized diquinoxalinylamino moieties as the peripheral groups have been synthesized and experimentally shown to manifest strong two‐photon absorption (2PA) and medium‐high up‐converted emission properties in the near‐IR (NIR) spectral region under the irradiation of femtosecond laser pulses. Tentative analysis of the structure–2PA property revealed that in the presented structural combination, diquinoxalinylamino units are useful 2PA‐enhancing subunits when properly incorporated. The π‐conjugation length of the central oligo‐(p‐phenylene) components was also found to be one of the key parameters that relates to the magnitude of the overall molecular 2PA properties in the studied molecular system, and this structural motif provides access to highly efficient two‐photon absorbers with large two‐photon action cross‐section values. A multi‐branched chromophore set, with ladder‐type oligo‐(p‐phenylenes) units as the central π‐bridges and functionalized diquinoxalinylamino moieties as the peripheries, has been synthesized and shown to exhibit strong two‐photon action cross‐section (ΦFδ) values and medium‐high up‐converted emission properties in the near‐IR (NIR) spectral region under the irradiation of femtosecond laser pulses.
    其他題名: Eur. J. Org. Chem
    出版者: Weinheim: WILEY-VCH Verlag
    出版日期: 2014-03
    出處: European journal of organic chemistry, 2014-03, Vol.2014 (8), p.1615-1621
    資源來源: Wiley Online Library - AutoHoldings Journals
    版權: Copyright © 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
    版權: Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
    識別號: ISSN: 1434-193X
    識別號: EISSN: 1099-0690
    識別號: DOI: 10.1002/ejoc.201301290
    Appears in Collections:[Department of Chemistry] journal & Dissertation

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