Matrix-Modulated Protonation Decoupling in Acrylonitrile Fluorophores: Toluene-Swollen PMMA for Multilevel Encryption and Logic Gate Fabrication

Stimuli-responsive organic fluorophores are fundamental candidates for high-security information encryption and intelligent molecular devices. Nevertheless, conventional acid-responsive systems suffer from uncontrolled protonation kinetics, simple binary optical switching, and limited capability to regulate solid-state sequential protonation. Herein, we construct a library of thiophene-acrylonitrile proton-responsive fluorophores bearing pyridine and dimethylamino terminal groups. The acrylonitrile-conjugated scaffold tunes proton affinity and frontier orbital energies, enabling solvent-dependent sequential protonation with distinct acid thresholds for different basic sites. Combined spectroscopic characterizations and quantum chemical calculations reveal the structure-protonation-photophysics correlation, confirming that stepwise protonation at two independent sites triggers tunable absorption and emission shifts. The key novelty of this work lies in matrix-mediated decoupling of sequential protonation: embedding the fluorophore within poly(methyl methacrylate) (PMMA) drastically alters protonation behavior relative to solution, since the polymer matrix restricts molecular and proton diffusion and suppresses full dual protonation. Toluene vapor-induced matrix swelling relieves these physical constraints and reactivates the sequential protonation cascade, delivering unique acid-solvent dual responsiveness exclusively accessible in solid polymer films. Utilizing this switchable protonation pathway, we realize ternary information encryption and a molecular SR logic gate, enabling hierarchical information release, decoy information masking, and precise chemical-to-optical signal conversion for multi-level data storage. This work establishes a matrix-modulated strategy to manipulate stepwise protonation in solid-state media, offering a versatile platform for high-capacity anti-counterfeiting tags and intelligent molecular optical devices.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-09-15
DOI
https://doi.org/10.1021/acsami.6c11921
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Matrix-Modulated Protonation Decoupling in Acrylonitrile Fluorophores: Toluene-Swollen PMMA for Multilevel Encryption and Logic Gate Fabrication

马法运, Meijing Li, Zujin Zhao, Jian Li et al.
ACS Applied Materials & Interfaces
Luminescence and Fluorescent Materials
article

Matrix-Modulated Protonation Decoupling in Acrylonitrile Fluorophores: Toluene-Swollen PMMA for Multilevel Encryption and Logic Gate Fabrication

马法运, Meijing Li, Zujin Zhao, Jian Li, Shijie Zhen, Hong Chen, Yingxiu Chen
article en

Abstract

Stimuli-responsive organic fluorophores are fundamental candidates for high-security information encryption and intelligent molecular devices. Nevertheless, conventional acid-responsive systems suffer from uncontrolled protonation kinetics, simple binary optical switching, and limited capability to regulate solid-state sequential protonation. Herein, we construct a library of thiophene-acrylonitrile proton-responsive fluorophores bearing pyridine and dimethylamino terminal groups. The acrylonitrile-conjugated scaffold tunes proton affinity and frontier orbital energies, enabling solvent-dependent sequential protonation with distinct acid thresholds for different basic sites. Combined spectroscopic characterizations and quantum chemical calculations reveal the structure-protonation-photophysics correlation, confirming that stepwise protonation at two independent sites triggers tunable absorption and emission shifts. The key novelty of this work lies in matrix-mediated decoupling of sequential protonation: embedding the fluorophore within poly(methyl methacrylate) (PMMA) drastically alters protonation behavior relative to solution, since the polymer matrix restricts molecular and proton diffusion and suppresses full dual protonation. Toluene vapor-induced matrix swelling relieves these physical constraints and reactivates the sequential protonation cascade, delivering unique acid-solvent dual responsiveness exclusively accessible in solid polymer films. Utilizing this switchable protonation pathway, we realize ternary information encryption and a molecular SR logic gate, enabling hierarchical information release, decoy information masking, and precise chemical-to-optical signal conversion for multi-level data storage. This work establishes a matrix-modulated strategy to manipulate stepwise protonation in solid-state media, offering a versatile platform for high-capacity anti-counterfeiting tags and intelligent molecular optical devices.

ACS Applied Materials & Interfaces
Guilin University of Aerospace Technology (CN), Guilin University of Technology (CN), Guilin University of Electronic Technology (CN), South China University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 25%
Luminescence and Fluorescent Materials
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