445027-76-9

Usage

Uses

Used in Chemical Reactions:
2,2'-Bipyridine, 4,4'-diheptylis used as a complexing agent for metal ions, facilitating the formation of stable metal complexes in various chemical reactions. This enhances the reactivity and selectivity of the reactions, making it a valuable tool in coordination chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, 2,2'-bipyridine, 4,4'-diheptylis used as a ligand to form metal complexes that can act as catalysts. These catalysts can improve the efficiency and selectivity of organic reactions, leading to the production of desired compounds with fewer side products.
Used in Pharmaceuticals:
2,2'-Bipyridine, 4,4'-diheptylis used in the pharmaceutical industry as a building block for the synthesis of various drug molecules. Its ability to form stable metal complexes can be exploited to create new drugs with improved properties, such as increased stability, solubility, or bioavailability.
Used in Materials Science:
In materials science, 2,2'-bipyridine, 4,4'-diheptylis used to create new materials with unique properties. Its ability to form metal complexes can be utilized to develop materials with enhanced electrical conductivity, magnetic properties, or optical characteristics, which can be applied in various technological applications.

Upstream product

• 1134-35-6 4,4'-dimethyl-2,2'-bipyridines 
• 110-53-2 1-Bromopentane 

Downstream Products

• 1587640-98-9 C₅₃H₅₃F₆N₃PtS₂ 
• 1587640-97-8 C₅₁H₄₈F₆N₂PtS₂ 
• 1587641-04-0 C₅₃H₅₃F₆N₃PtS₂ 
• 1587641-03-9 C₅₁H₄₈F₆N₂PtS₂ 

Relevant academic research and scientific papers

New insights into the reaction of t-butylhydroperoxide with dichloro- and dimethyl(dioxo)molybdenum(VI)

Lewis-base adducts of dichlorodioxomolybdenum(VI) and dimethyldioxomolybdenum(VI) react in an equilibrium reaction with excess t-butylhydroperoxide (TBHP) under the formation of a seven-coordinated molybdenum(VI) complexes displaying a η1-alkyl

Self-assembled bilayers as an anchoring strategy: Catalysts, chromophores, and chromophore-catalyst assemblies

Anchoring strategies for immobilization of molecular catalysts, chromophores, and chromophorecatalyst assemblies on electrode surfaces play an important role in solar energy conversion devices such as dyesensitized solar cells and dye-sensitized photoelectrosynthesis cells. They are also important in interfacial studies with surface-bound molecules including electron-transfer dynamics and mechanistic studies related to small molecule activation catalysis. Significant progress has been made in this area, but many challenges remain in terms of stability, synthetic complexity, and versatility. We report here a new anchoring strategy based on selfassembled bilayers. This strategy takes advantage of noncovalent interactions between long alkyl chains chemically bound to a metal-oxide electrode surface and long alkyl chains on the molecule being anchored. The new methodology is applicable to the heterogenization of both catalysts and chromophores as well as to the in situ "synthesis" of chromophore-catalyst assemblies on the electrode surface.

Amphiphilic polypyridyl ruthenium complexes: Synthesis, characterization and aggregation studies

Synthesis and characterization of five amphiphilic ruthenium(II) complexes of the type [Ru(Cn)3].(PF6)2 (Cn = 4,4′-dialkyl-2,2′-bipyridine, n = 5(4,4′-dipentyl), 6(4,4′-dihexyl), 7(4,4′-diheptyl), 8(4,4′-dioctyl), 9(4,4′-dinonyl)) have been investigated. Single crystal X-ray structures of 4,4′-dipentyl-2,2′-bipyridine (C5), 4,4′-dioctyl-2,2′-bipyridine (C8) ligands and [Ru(C5)3](PF6)2 complex are elucidated. Structural inferences are corroborated through the density functional theory. Molecular aggregations in these systems in aqueous and non-aqueous media have further been analyzed from FESEM experiments.