144342-48-3

Usage

Uses

Used in Coordination Chemistry:
2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethylis utilized as a chelating ligand for the formation of stable complexes with metal ions. Its ability to bind with metals contributes to its use in the development of new coordination compounds with potential applications in catalysis, sensing, and materials science.
Used in Organic Synthesis:
In the field of organic synthesis, 2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethylserves as a versatile building block for the creation of novel organic molecules. Its unique furan ring and bipyridine structure allow for the synthesis of complex organic compounds with potential applications in pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Material Science:
2,2'-Bipyridine, 4,4'-di-2-furanyl-6,6'-dimethylis employed in material science for the development of new materials with specific properties. Its incorporation into polymers, for instance, can lead to materials with improved conductivity, stability, or other desirable characteristics, making it valuable for applications in electronics, sensors, and other advanced technologies.

Upstream product

• 92152-08-4 (1E,5E)-1,6-di(furan-2-yl)hexa-1,5-diene-3,4-dione 
• 42508-60-1 1-(2-oxopropyl)pyridinium chloride 
• 92152-08-4 1,6-di-furan-2-yl-hexa-1,5-diene-3,4-dione 
• 17282-41-6 N-acetonylpyridinium bromide 

Downstream Products

• 117330-40-2 dimethyl 6,6'-dimethyl-2,2'-bipyridine-4,4'-dicarboxylate 
• 117330-41-3 4,4'-dimethyl 6,6'-bis(bromomethyl)-[2,2'-bipyridine]-4,4'-dicarboxylate 
• 144342-49-4 6,6′-dimethyl-2,2′-bipyridine-4,4′-dicarboxylic acid 

Relevant academic research and scientific papers

Lanthanide-series compound and preparation method and application thereof

The invention provides a lanthanide-series compound and a preparation method and an application thereof; the lanthanide-series compound has the chemical structural formula described in the description. The lanthanide-series compound has no inversion center, is beneficial for the compound to generate higher-brightness fluorescence, and enables a strongest emission peak to be used in a fluorescence analysis peak of time-resolved fluorescence immunoassay; and at the same time, the compound has relatively strong stability, and still can be used for marking and testing after being placed for a certain time.

Copper(i) complexes of 6,6′-disubstituted 2,2′-bipyridine dicarboxylic acids: New complexes for incorporation into copper-based dye sensitized solar cells (DSCs)

Synthetic approaches to 6,6′-disubstituted-2,2′-bipyridine ligands bearing carboxylic acid substituents at the 4,4′ or 5,5′-positions are described. Copper(i) complexes with these ligands have been prepared for use in copper-based dye-sensitized solar cells. The single-crystal structures of 6,6′-dimethyl-2,2′-bipyridine-4, 4′-dicarboxylic acid (H24), [H36][CF 3CO2]·2CF3CO2H (H 26 = 6,6′-diphenyl-2,2′-bipyridine-4,4′- dicarboxylic acid) and 4[Cu(H22)(H2)]·3H2O (H 22 = 6,6′-dimethyl-2,2′-bipyridine-5,5′- dicarboxylic acid) are described, as well as those of the intermediates (1E,5E)-1,6-di(2-furyl)hexa-1,5-diene-3,4-dione and 4,4′-di(2-furyl)-6, 6′-dimethyl-2,2′-bipyridine (3), and the copper(i) complex [Cu(3)2][PF6]. The roles that classical and non-classical hydrogen bonding and π-stacking interactions play in determining the solid-state packing in these structures are discussed. Preliminary studies of DSCs with these complexes are reported. The Royal Society of Chemistry 2009.