A simple AIE-active salicylideneaniline towards bimodal encryption-decryption with unique ESIPT-inhibited amorphous state

Xu Min Cai*, Weiren Zhong, Ziwei Deng, Yuting Lin, Zhenguo Tang, Xuedan Zhang, Jianyu Zhang, Wenjin Wang, Shenlin Huang, Zheng Zhao, Ben Zhong Tang

*Corresponding author for this work

Research output: Contribution to journalJournal Articlepeer-review

24 Citations (Scopus)

Abstract

Multimodal encryption-decryption with photochromism has been proved to ensure information security with great feasibility and operability. However, most of the photochromic materials are applied in single-mode encryption-decryption and highly dependent on crystallization, requiring long manufacturing time and lacking of controllability. Hence, amorphous materials with simple preparation and bimodal encryption-decryption are of good alternates. Herein, we have succeeded in developing an aggregation-induced emission-active and photochromic ATPA-SAB with crystalline form via introduction of the propeller-like and bulky triphenylamine (TPA). Expectedly, the amorphous materials can be obtained by fast precipitation. Examining its amorphous structures, the intramolecular N‧‧‧H distances of around 4.000 Å is largely over the normal intramolecular hydrogen bond of circa 1.800 Å, impeding the intrinsic excited-state intramolecular proton transfer process (ESIPT) for the first time, hence prohibiting photochromism. This work not only provides a strategy to construct amorphous materials and inhibit ESIPT process with TPA, but also applies both crystalline and amorphous materials for bimodal encryption-decryption to upgrade information security.

Original languageEnglish
Article number143353
JournalChemical Engineering Journal
Volume466
DOIs
Publication statusPublished - 15 Jun 2023
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2023 Elsevier B.V.

Keywords

  • Aggregation-induced emission
  • Amorphous
  • Bimodal encryption-decryption
  • Excited-state intramolecular proton transfer
  • Photochromism

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