10129-71-2

Usage

Uses

Used in Photochemical Reactions:
2,6-bis(2-phenylvinyl)pyridine is used as a sensitizer to enhance the efficiency of photochemical reactions. Its ability to absorb light and transfer energy to other molecules makes it a key component in processes that require light-induced chemical transformations.
Used in Organic Light-Emitting Diodes (OLEDs):
In the electronics industry, 2,6-bis(2-phenylvinyl)pyridine serves as a phosphorescent emitter in OLEDs. Its high quantum yield and fluorescence properties contribute to the development of high-performance display and lighting technologies, offering improved energy efficiency and brightness.
Used in Advanced Technology Development:
2,6-bis(2-phenylvinyl)pyridine is utilized in the research and development of new technologies in electronics and photonics. Its unique properties make it a promising candidate for applications that require high-performance materials with specific light-emitting or light-sensitive characteristics.
Despite the potential applications of 2,6-bis(2-phenylvinyl)pyridine, ongoing research is essential to fully explore and maximize its capabilities in various technological and scientific domains.

InChI:InChI=1/C21H17N/c1-3-8-18(9-4-1)14-16-20-12-7-13-21(22-20)17-15-19-10-5-2-6-11-19/h1-17H/b16-14+,17-15+

Upstream product

• 109-06-8 α-picoline 
• 100-52-7 benzaldehyde 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 108-48-5 2,6-dimethylpyridine 
• 1195-59-1 2.6-bis(hydroxymethyl)pyridine 
• 140-29-4 phenylacetonitrile 
• 100-42-5 styrene 
• 626-05-1 2,6-Dibromopyridine 

Downstream Products

• 818377-18-3 Norlobelane 
• 2893-33-6 pyridine-2,6-dinitrile 
• 5431-44-7 2,6-Pyridinedicarboxaldehyde 
• 31250-16-5 [2-(2-chloro-2-oxoethoxy)phenoxy]acetyl chloride 
• 856849-90-6 2,6-bis-(α,β-dibromo-phenethyl)-pyridine 
• 68031-94-7 2,6-bis (2-phenylethyl) pyridine 

Relevant academic research and scientific papers

Tandem Acceptorless Dehydrogenative Coupling-Decyanation under Nickel Catalysis

The development of new catalytic processes based on abundantly available starting materials by cheap metals is always a fascinating task and marks an important transition in the chemical industry. Herein, a nickel-catalyzed acceptorless dehydrogenative coupling of alcohols with nitriles followed by decyanation of nitriles to access diversely substituted olefins is reported. This unprecedented C=C bond-forming methodology takes place in a tandem manner with the formation of formamide as a sole byproduct. The significant advantages of this strategy are the low-cost nickel catalyst, good functional group compatibility (ether, thioether, halo, cyano, ester, amino, N/O/S heterocycles; 43 examples), synthetic convenience, and high reaction selectivity and efficiency.

Synthesis of dicyanopyridines

Synthesis of the title compounds in four steps using inexpensive collidine and lutidine as starting materials is described.

Organostannoxane-supported Pd(0) nanoparticles as efficient catalysts for Heck-coupling reactions

A new functional organostannoxane cage, SnP, that contains phosphine ligands in its periphery has been structurally utilized as support palladium(0) nanoparticles SnPPd. The latter was shown to catalyze the Heck coupling reactions of wide variety of functionalities efficiently.