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Harnessing Molecular Isomerization in Polymer Gels for Sequential Logic Encryption and Anticounterfeiting

Overview
Journal Sci Adv
Specialties Biology
Science
Date 2022 Nov 2
PMID 36322650
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Abstract

Using smart photochromic and luminescent tissues in camouflage/cloaking of natural creatures has inspired efforts to develop synthetic stimuli-responsive materials for data encryption and anticounterfeiting. Although many optical data-encryption materials have been reported, they generally require only one or a simple combination of few stimuli for decryptions and rarely offer output corruptibility that prevents trial-and-error attacks. Here, we report a series of multiresponsive donor-acceptor Stenhouse adducts (DASAs) with unprecedented switching behavior and controlled reversibility via diamine conformational locking and substrate free-volume engineering and their capability of sequential logic encryption (SLE). Being analogous to the digital circuits, the output of DASA gel-based data-encryption system depends not only on the present input stimulus but also on the sequence of past inputs. Incorrect inputs/sequences generate substantial fake information and lead attackers to the point of no return. This work offers new design concepts for advanced data-encryption materials that operate via SLE, paving the path toward advanced encryptions beyond digital circuit approaches.

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References
1.
Noirbent G, Xu Y, Bonardi A, Duval S, Gigmes D, Lalevee J . New Donor-Acceptor Stenhouse Adducts as Visible and Near Infrared Light Polymerization Photoinitiators. Molecules. 2020; 25(10). PMC: 7287840. DOI: 10.3390/molecules25102317. View

2.
Broman S, Petersen M, Tortzen C, Kadziola A, Kilsa K, Brondsted Nielsen M . Arylethynyl derivatives of the dihydroazulene/vinylheptafulvene photo/thermoswitch: tuning the switching event. J Am Chem Soc. 2010; 132(26):9165-74. DOI: 10.1021/ja103235g. View

3.
Lee J, Seo S, Kim J . Rapid Light-Driven Color Transition of Novel Photoresponsive Polydiacetylene Molecules. ACS Appl Mater Interfaces. 2018; 10(4):3164-3169. DOI: 10.1021/acsami.7b17104. View

4.
Mao L, Wang Z, Duan Y, Xiong C, He C, Deng X . Designing of Rewritable Paper by Hydrochromic Donor-Acceptor Stenhouse Adducts. ACS Nano. 2021; 15(6):10384-10392. DOI: 10.1021/acsnano.1c02629. View

5.
Minkin V . Photo-, thermo-, solvato-, and electrochromic spiroheterocyclic compounds. Chem Rev. 2004; 104(5):2751-76. DOI: 10.1021/cr020088u. View