70936-44-6

Upstream product

• 16456-81-8 meso-tetraphenylporphyrin iron(III) chloride 
• 100-63-0 phenylhydrazine 
• 119907-38-9 (tetraphenylporphyrine)Fe(III)CH₂C₆H₅ 
• 83219-61-8 Fe(C₂₀H₈N₃(C₆H₅)4N(C₆H₅))Cl 

Downstream Products

• 16456-81-8 meso-tetraphenylporphyrin iron(III) chloride 
• 16591-56-3 5,10,15,20-tetraphenyl porphyrin iron 
• 89672-69-5 {(C₂₀H₈(C₆H₅)4N₄)Fe(C₆H₅)(NO)} 
• 83219-61-8 Fe(C₂₀H₈N₃(C₆H₅)4N(C₆H₅))Cl 

Relevant academic research and scientific papers

Kinetics, mechanism and thermodynamics of iron carbon bond dissociation in organoiron porphyrin complexes

Thermolysis of Fe(P)R (P = octaethylporphyrinato dianion, R = C6H5, CH3, C2H5, CH2C(CH3)3; P = tetraphenylporphyrinato dianion, R = C6H5; P = tet

SYNTHESE ET CARACTERISATION PAR RMN 1H D'ALKYL(ARYL)FERRIPORPHYRINES A LIAISON ? METAL-CARBONE

A series of alkyl(aryl)iron(III) porphyrins with a metal-carbon ? bond has been prepared either by action of an organomagnesium compound on iron(III) chloride porphyrins or by oxidative addition of alkyl halides to iron(I) porphyrins. 1H NMR data have been used to characterize the products obtained.