Photochromic compounds have attracted much attention for their potential applications in photo-actuators, optoelectronic devices and optical recording techniques. This interest is driven by their key photochemical and photophysical properties, which can be reversibly modulated by light irradiation. Among them, diarylethene compounds have garnered extensive investigation due to their excellent thermal stability of both open- and closed-form isomers, robust fatigue resistance, high photocyclization quantum yield and good photochromic performance in both solution and solid phases. However, a notable limitation in expanding the utility of diarylethene compounds is the necessity for ultraviolet light to induce their photochromism. This requirement poses challenges, as ultraviolet light can be detrimental to biological tissues, and its penetration is often restricted in various media. This review provides an overview of design strategies employed in the development of visible-light-responsive diarylethene compounds. These design strategies serve as a guideline for molecular design, with the potential to significantly broaden the applications of all-visible-light-activated diarylethene compounds in the realms of materials science and biomedical science.
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http://dx.doi.org/10.3390/molecules29215202 | DOI Listing |
ACS Omega
December 2024
Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, Virginia 23529, United States.
Diarylethenes (DAEs) are an important class of photoswitchable compounds that typically undergo reversible photochemical conversions between the open and closed cyclized forms upon treatment with UV light or visible light. In this study, we introduced thioacid functional groups to several photochromic dithienylethene (DTE) derivatives and established a method that can be used to prepare these photoswitchable thioacids. Four thioacid-functionalized diarylethene derivatives were synthesized through the activation of carboxylic acids with -hydroxysuccinimide, followed by reactions with sodium hydrosulfide with yields over 90%.
View Article and Find Full Text PDFInorg Chem
November 2024
Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Liangxiang Campus, Beijing Institute of Technology, Beijing 102488, People's Republic of China.
A diarylethene ligand-anchored two-dimensional Hofmann-type compound [Fe(BTEPy){Pt(CN)}](CHOH) (BTEPy = 1,2-bis[2-methyl-5-(4-pyridyl)-3-thienyl]cyclopentene) is synthesized, which undergoes a two-step spin-state transition and dual photoinduced magnetic switching.
View Article and Find Full Text PDFMolecules
November 2024
School of Pharmacy, Jining Medical University, Rizhao 276826, China.
Photochromic compounds have attracted much attention for their potential applications in photo-actuators, optoelectronic devices and optical recording techniques. This interest is driven by their key photochemical and photophysical properties, which can be reversibly modulated by light irradiation. Among them, diarylethene compounds have garnered extensive investigation due to their excellent thermal stability of both open- and closed-form isomers, robust fatigue resistance, high photocyclization quantum yield and good photochromic performance in both solution and solid phases.
View Article and Find Full Text PDFChem Sci
September 2024
Université Paris-Saclay, ENS Paris-Saclay, CNRS, PPSM 91190 Gif-sur-Yvette France
Photochromic compounds are promising for a variety of applications, including molecular solar thermal (MOST) energy storage. The energy release step and cyclability are critical issues to be addressed for the development of this technology. We report herein the synthesis and characterization of two diarylethene molecules featuring one (1) or two (2) pyridine groups as protonatable moieties.
View Article and Find Full Text PDFChemphyschem
September 2024
Division of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara, 630-0192, Japan.
Two novel diarylethene-fused subporphyrinoids were prepared and characterized. A mono diarylethene derivative was obtained via a statistical condensation reaction with 2 eq. of 1,2-dicyanobenzene and 1 eq.
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