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January 14, 2026RSC Advances0 citationsOpen Access

Molecular mechanism of biocompatible clusteroluminogens from citric acid and l -lysine

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QZQiannan ZhangPSPingchuan SunBLBaohui Li

Key Points

  • The research aims to elucidate the molecular mechanisms behind clusteroluminogens synthesized from citric acid and L-lysine.
  • One-step synthesis of luminescent materials using citric acid and L-lysine.
  • Assessment of fluorescence and afterglow properties of the synthesized materials.
  • Analysis of ionic bond interactions affecting electron transitions.
  • Achieved 43.2% fluorescence in the materials.
  • Observed ultralong room temperature phosphorescence (RTP) lasting 5 seconds.
  • Interactions between molecular components enhance electron transitions, facilitating clusteroluminescence.

Abstract

One-step synthesis of dual-mode luminescent materials using CA/Lys gives high fluorescence (43.2%) and ultralong RTP (5 s). Study shows interactions/ionic bonds boost electron transitions, explaining clusteroluminescence in non-conjugated systems.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/696719c1c0d1e3cfbfce92d9https://doi.org/10.1039/d5ra09240j
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