1586038-80-3

Upstream product

• 550348-56-6 4-(4-bromo-5-methylthiophen-2-yl)benzaldehyde 
• 550348-57-7 3-bromo-5-(4-(1,3-dioxolan-2-yl)phenyl)-2-methylthiophene 
• 559-40-0 octaperfluorocyclopentene 
• 58863-48-2 3-bromo-2-methyl-1-benzofuran 
• 1427283-27-9 1-(2-methyl-1-benzofuran-3-yl)-2-[2-methyl-5-(4-1,3-dioxolane-phenyl)-3-thienyl]perfluorocyclopentene 
• 1586038-83-6 C₂₆H₁₆F₆O₂S 

Downstream Products

• 1586038-83-6 C₂₆H₁₆F₆O₂S 

Relevant academic research and scientific papers

Photochromism of a novel asymmetrical diarylethene with a (formyloxyethoxy)ethyl-linked naphthalimide moiety

A novel asymmetrical diarylethene with a (formyloxyethoxy)ethyl-linked naphthalimide unit was synthesized, and its photochromic and fluorescence properties were systematically investigated in both solution and a poly(metyl methacrylate) film. The diarylethene showed significant photochromism and notable fluorescence switching properties upon irradiation with ultraviolet/visible light. Compared with the parent diarylethene, introduction of the naphthalimide moiety was effective to increase the molar absorption coefficient, the fluorescence quantum yield, and fluorescent modulation efficiency of the diarylethene. Copyright

A multi-addressable molecular switch based on a novel diarylethene with an imidazo [4,5-f] [1,10] phenanthroline unit

A novel unsymmetrical diarylethene with an imidazo [4,5-f] [1,10] phenanthroline unit has been synthesized, and its properties including photochromism and fluorescence have been investigated. It showed favorable photochromism and functioned as notable fluorescence switches by photoirradiation in both solution and a poly (methylmethacrylate) film. Moreover, the interaction between the phenanthroline unit of its closed-ring isomer with trifluoroacetic acid caused a notable change in its absorption, accompanied by an evident color change from magenta to slateblue. Its fluorescence could be modulated by trifluoroacetic acid and triethylamine. By adding enough amount of trifluoroacetic acid in chloroform, its emission peak hypochromatic shifted from 501 nm to 456 nm, and the intensity increased significantly with a concomitant change of color from bright cyan to bright blue. However, its emission intensity decreased notably by 95% with a fluorescence color change from bright cyan to dark gray by the addition of triethylamine. Copyright