733746-88-8

Upstream product

• 185223-97-6 1′-(diphenylphosphino)-1-bromoferrocene 
• 814-49-3 diethyl chlorophosphate 

Downstream Products

• 916899-19-9 [Hg(μ-Br)Br(diethyl [1'-(diphenylphosphanyl)ferrocenyl]phosphonate]-κP2)]2 
• 916899-16-6 [ZnBr2(diethyl [1'-(diphenylphosphanyl)ferrocenyl]phosphonate]-κ2O1,P2)] 
• 916899-14-4 trans-[Pd(μ-Cl)Cl(diethyl [1'-(diphenylphosphanyl)ferrocenyl]phosphonate]-κP2)]2 
• 733746-87-7 1-diphenylphosphino-1'-phosphinoferrocene 

Relevant academic research and scientific papers

Synthesis and structural characterisation of palladium and group-12 metal complexes with a hybrid phosphanylphosphonate ferrocene ligand

Diethyl [1′-(diphenylphosphanyl)ferrocenyl]phosphonate (1) was synthesised by stepwise metallation/functionalisation of 1,1′- dibromoferrocene and studied as a ligand for palladium(II) and group-12 metals. Treatment of [PdCl2(cod)] (cod = ηsup

Synthesis and structural characterisation of 1’-(diphenylphosphino)ferrocene-1-phosphonic acid, its ammonium salts and Pd(II) complexes

A new polar phosphinoferrocene ligand, viz. 1’-(diphenylphosphino)ferrocene-1-phosphonic acid (H2L), was prepared by hydrolysis of the corresponding phosphonate ethyl ester. However, the compound is relatively unstable, gradually decomposing up