1089731-76-9

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 325142-81-2 4,4,5,5-tetramethyl-2-(2,3,4,5,6-pentafluorophenyl)-1,3,2-dioxaborolane 
• 1582-24-7 pentafluorophenylboronic acid 
• 879-05-0 2,3,4,5,6-pentafluorophenylmagnesium bromide 
• 84-65-1 9,10-phenanthrenequinone 
• 363-72-4 Pentafluorobenzene 

Downstream Products

• 1238896-86-0 C₆H₆*C₂₆H₈F₁₀ 
• 1238896-88-2 C₄H₈O₂*C₂₆H₈F₁₀ 

Relevant academic research and scientific papers

Palladium-Catalyzed Solid-State Polyfluoroarylation of Aryl Halides Using Mechanochemistry

The Suzuki–Miyaura cross-coupling between polyfluorinated arylboron nucleophiles and aryl halides enables the efficient construction of polyfluorinated structural motifs frequently found in organic materials and catalysts. A key challenge associated with

Blue/violet diphenylanthracene chemiluminescent fluorescers

Compounds are disclosed for the production of chemiluminescent light, particularly for the production of blue/violet light within the range of about 390 nm to less than 438 nm, and most particularly to the use of compounds composed of symmetrically and asymmetrically substituted anthracenes which are effective for increasing the production of such blue/violet light when used as fluorescers in conjunction with chemiluminescent systems. These systems utilize derivatives of 9,10-diphenylanthracene containing one or more fluorines As shown in General Formulae 1-3. The variables shown in Formulae 1-3 are defined in the specification.

Blue/violet diphenylanthracene chemiluminescent fluorescers

Compounds are disclosed for the production of chemiluminescent light, particularly for the production of blue/violet light within the range of about 390 nm to less than 438 nm, and most particularly to the use of compounds composed of symmetrically and asymmetrically substituted anthracenes which are effective for increasing the production of such blue/violet light when used as fluorescers in conjunction with chemiluminescent systems. These systems utilize derivatives of 9,10-diphenylanthracene containing one or more fluorines As shown in General Formulae 1-3. The variables shown in Formulae 1-3 are defined in the specification.

Meso-disubstituted anthracenes with fluorine-containing groups: Synthesis, light-emitting characteristics, and photostability

(Chemical Equation Presented) Synthesis, photophysical properties, and photostability of 9,10-disubstituted anthracenes with fluorine-containing groups (FCG) are described. The values of Φf and λem greatly go up by the meso-substitution with FCG, and a nice corelationship between Φf and Aπ (magnitude of π conjugation length in the excited single state) is observed. The C6F5 group at the meso positions exhibits an excellent ability in the photostability as well as in the emission efficiency.