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<p>Photochemical sensing demands systems that adjust their optical properties without altering chromophore structure. Here, we report CPCQ, a thermally activated delayed fluorescence (TADF)-active macrocycle, as a responsive platform for optical sensing. CPCQ shows a photoluminescence quantum yield (PLQY) of 78%, a delayed lifetime of 243 ns, and an efficient reverse intersystem crossing rate of 2.68 × 10⁷ s⁻¹. Unlike conventional fluorescent and TADF emitters, CPCQ with cyclic array of four TADF active donor-acceptors enables reversible state switching of its emission mechanism. Electron-deficient guests form exciplexes with reducing fluorescence and shifting emission. In contrast, electron-rich guests enhance delayed fluorescence (248 ns) via the heavy atom effect. Oxygen quenches charge-transfer emission and restores blue-shifted locally excited (LE) emission. Strikingly, hydrogen flips the effect, triples LE emission (k<sub>r</sub> = 2.07 × 10<sup>8 </sup>s<sup>-1</sup>, PLQY = 93%), and hints at superradiance from cooperative behavior of donor–acceptor units. These adaptive responses establish CPCQ as a highly sensitive and selective molecular tool for next-generation sensing and optoelectronic applications.</p><p></p>

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A state-switchable TADF macrocycle for multi-analyte sensing and hydrogen gas-driven emission enhancement

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年3月2日

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  • Raktim Deka,
  • Dinesh Singh,
  • Manjeet Singh,
  • Kshatresh Dutta Dubey,
  • Debdas Ray

摘要

Photochemical sensing demands systems that adjust their optical properties without altering chromophore structure. Here, we report CPCQ, a thermally activated delayed fluorescence (TADF)-active macrocycle, as a responsive platform for optical sensing. CPCQ shows a photoluminescence quantum yield (PLQY) of 78%, a delayed lifetime of 243 ns, and an efficient reverse intersystem crossing rate of 2.68 × 10⁷ s⁻¹. Unlike conventional fluorescent and TADF emitters, CPCQ with cyclic array of four TADF active donor-acceptors enables reversible state switching of its emission mechanism. Electron-deficient guests form exciplexes with reducing fluorescence and shifting emission. In contrast, electron-rich guests enhance delayed fluorescence (248 ns) via the heavy atom effect. Oxygen quenches charge-transfer emission and restores blue-shifted locally excited (LE) emission. Strikingly, hydrogen flips the effect, triples LE emission (kr = 2.07 × 108 s-1, PLQY = 93%), and hints at superradiance from cooperative behavior of donor–acceptor units. These adaptive responses establish CPCQ as a highly sensitive and selective molecular tool for next-generation sensing and optoelectronic applications.