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Usage

Uses

Used in Coordination Chemistry:
1,2-Bis(dicyclohexylphosphino)benzene is used as a ligand for forming stable complexes with transition metals, which is crucial for enhancing the reactivity and stability of metal ions in various chemical reactions.
Used in Catalysis:
In the catalysis industry, 1,2-bis(dicyclohexylphosphino)benzene is used as a ligand to create catalysts that facilitate and expedite chemical reactions. Its ability to chelate with metal ions contributes to the development of efficient and selective catalysts.
Used in Organic Synthesis:
1,2-Bis(dicyclohexylphosphino)benzene is utilized in organic synthesis as a ligand to support the formation of complex organic molecules. Its structural properties enable the stabilization of metal-mediated reactions, leading to the successful synthesis of desired products.
Used in Materials Science:
In materials science, 1,2-bis(dicyclohexylphosphino)benzene is employed in the development of new materials with specific properties. Its role as a ligand in metal complexes can influence the physical and chemical characteristics of these materials, making it an important component in material design and innovation.

Upstream product

• 82495-67-8 1,2-bis(dichlorophosphanyl)benzene 
• 931-50-0 cyclohexylmagnesium bromide 
• 108-85-0 1-bromocyclohexane 

Relevant academic research and scientific papers

Nickel-catalyzed amination of aryl fluorides with primary amines

The Ni-catalyzed cross-coupling reaction between aryl fluorides and primary amines was enabled by the 1,2-bis(dicyclohexylphosphino)benzene (DCYPBz) or 1,2-bis(dicyclohexylphosphino)ethane (DCYPE) ligands. Both N-alkyl- and N-aryl-substituted primary amin

Method for synthesizing alpha, beta-unsaturated acid by using formic acid and alkine

The invention relates to a method for synthesizing alpha, beta-unsaturated acid by using formic acid and alkine, in particular to a method for synthesizing alpha, beta-unsaturated acid by using formic acid and alkine under the effect of a nickel catalyst. The consumption of the catalyst is 0.01 to 2 mol percent of the quantity of a substrate substance; the consumption of estolide is 3 to 30 mol percent of the quantity of the substrate substance; the pressure of acetylene gas is 1 to 10 MPa; the reaction temperature is 25 to 100 DEG C; the reaction time is 5 to 12 hours. The method has the advantages that the existing alkine hydrocarboxylation defects are overcome; the use of toxic carbon monoxide gas does not needed; the reaction conditions of the whole process are mild; the efficiency is high; the selectivity is good; the method belongs to a method for preparing the alpha, beta-unsaturated acid with the advantages that the method conforms to green chemistry and has good application aspects; good industrial application prospects are realized.