257933-26-9

Upstream product

• 1129-30-2 2,6-Diacetylpyridine 
• 579-66-8 2,6-diethylaniline 
• 420119-94-4 2,6-bis-[1-(2,6- diethylphenylimino)ethyl]pyridine 

Downstream Products

• 863328-52-3 iron(II)(bis(2,6-diethylphenyl-iminomethyl)pyridine) monomethyl 
• 863328-56-7 iron(II)(bis(2,6-Et₂-phenyl-iminomethyl)pyridine)(CH₂SiMe₃) 
• 863328-55-6 iron(II)(bis(2,6-Et₂-phenyl-iminomethyl)pyridine)(CH₂SiMe₃)2 
• 863328-49-8 iron(II)(bis(2,6-diethylphenyl-iminomethyl)pyridine) monochloride 
• 1005483-58-8 ((Et)PDI)FeCH₂CMe₃ 

Relevant academic research and scientific papers

Electronic Effects of the Backbone on Bis(imino)pyridyliron(II)-Catalyzed Ethylene Polymerization

A series of bis(imino)pyridyl iron(II) complexes 1–5 with electron-donating and -withdrawing substituents on the backbone of the ligand have been synthesized and characterized. Activated with methylaluminoxane (MAO), ethylene polymerization by these iron(

New bis(imino)pyridine complexes of iron(II) and iron(III), and their catalytic-activity in the mukaiyama aldol reaction

New iron(II) and iron(III) complexes bearing bis(imino)pyridine ligands were synthesized and successfully applied to the Mukaiyama aldol reaction. The two complexes [FeCl2 L] (L = bis(imino)pyridine ligand, 55% isolated yield) and [LFe(μCl)sub

Heterogenized iron(II) complexes as highly active ethene polymerization catalysts

The synthesis of new iron(II) diiminopyridine complexes and their heterogenization to give highly active ethene polymerization catalysts is described. The ligands are characterized by 1H NMR, 13C NMR spectroscopy and GC/MS. The compl