Fe(III) meso-Tetra (p-aminophenyl) Porphine Chloride

Product Number: 41404; CAS Number: 99651-88-4

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Fe(III) meso-Tetra (p-aminophenyl) Porphine Chloride CAS: 99651-88-4 MDL: MFCD03453186

Molecular weight: 764.076 g/mol

Molecular Formula: C44H32ClFeN8

CAS Number: 99651-88-4

Storage: Store at room temperature, protect from light

Synonyms: Iron(3+) chloride 5,10,15,20-tetrakis(4-aminophenyl)porphine-21,22-diide (1:1:1), Benzenamine, 4,4′,4”,4”’-(21H,22H-porphine-5,10,15,20-tetrayl)tetrakis-, iron(3+) salt, hydrochloride (1:1:1), Chlorure 5,10,15,20-tétrakis(4-aminophényl)porphine-21,22-diide de fer(3+) (1:1:1), Eisen(3+)chlorid-5,10,15,20-tetrakis(4-aminophenyl)porphin-21,22-diid (1:1:1), Iron(3+) chloride 5,10,15,20-tetrakis(4-aminophenyl)porphine-21,22-diide (1:1:1), (SP-4-1)-((4,4′,4”,4”’-(21H,23H-Porpine-5,10,15,20-tetrayl)tetrakis(benzenaminato))(2-)-N21,N22,N23,N24)iron(1+)chloride, 5,10,15,20-TETRAKIS-(4-AMINOPHENYL)-PORPHYRIN-FE(III) CHLORIDE, 87097-67-4, 99651-88-4, Iron(1+), ((4,4′,4′‘,4”’-(21H,23H-porpine-5,10,15,20-tetrayl)tetrakis(benzenaminato))(2-)-N21,N22,N23,N24)-, chloride, (SP-4-1)-

Field of Interest: Catalysis, Covalent Organic Frameworks, Modified Electrodes

Background: Fe(III) meso-Tetra (p-aminophenyl) Porphine Chloride is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals. Fe(III) meso-Tetra (p-aminophenyl) Porphine Chloride  was used to modify the surfaces of electrodes for catalytic purposes.1,2

References: 

1.) Elliot, et al. Catalytic reduction of some alkyl halides by iron porphyrin modified carbon electrodes. Journal of Electroanalytical Chemistry and Interfacial Electrochemistry. Volume 119, Issue 2, 10 March 1981, Pages 395-401. https://doi.org/10.1016/S0022-0728(81)80071-X

2.) Goya, et al. Surface Effect on Fe (III)Poly-(Tetraaminophenyl) Porphyrin Modified Electrodes After Electrocatalytic Reactions. An Electrochemical and Atomic Force Microscopy Study. Int. J. Electrochem. Sci., 6 (2011) 4984 – 4998. 

3.) Xu, et al. Three-Dimensional Covalent Organic Frameworks with she Topology. J. Am. Chem. Soc. 2022, 144, 40, 18511–18517. https://doi.org/10.1021/jacs.2c07733

4.) Xeng, et al. Impregnation of metal ions into porphyrin-based imine gels to modulate guest uptake and to assemble a catalytic microfluidic reactor. J. Mater. Chem. A, 2016,4, 8328-8336. https://doi.org/10.1039/C6TA01035K

Categories

Porphyrins
Metal

Iron Porphyrins
Porphyrin Family

A4 Porphyrins, Amino Porphyrins, Metallo Porphyrins, Tetra-Phenyl Porphine Derivatives
Porphyrin Substitution

Amino-Phenyl Substituted Porphyrins, Meso-Substituted Porphyrins, Phenyl Substituted Porphyrins
Functional Groups

Amine, Amino

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