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(tetraphenylporphinato)Fe-O-O-Fe(tetraphenylporphinato) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73146-62-0

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73146-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73146-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,4 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73146-62:
(7*7)+(6*3)+(5*1)+(4*4)+(3*6)+(2*6)+(1*2)=120
120 % 10 = 0
So 73146-62-0 is a valid CAS Registry Number.

73146-62-0Downstream Products

73146-62-0Relevant academic research and scientific papers

Fluoride Ion Coordination Chemistry of Iron(II) Porphyrins: Unique Spectral Properties and Associated Dioxygen Activation Chemistry of the Fluoroiron(II) Complex

Yu, Byung-Soo,Goff, Harold M.

, p. 6558 - 6562 (1989)

Fluoroiron(II) porphyrin anionic complexes are generated in a variety of organic solvents by addition of tetrabutylammonium fluoride to the respective square-planar iron(II) porphyrin.The paramagnetic fluoroiron(II) tetraphenylporphyrin pyrrole proton NMR chemical shift value of 30.3 ppm resembles that for the corresponding hydroxide ion complex and is consistent with a high-spin iron(II) configuration.This even-spin complex surprisingly exhibits a broad 750 G X-band EPR signal at liquid helium temperature.Such a signal is expected only for a complex with alow-symmetry ligand field component.A very large Moessbauer quadrupole splitting parameter of 4.06 mm/s (78 K) serves to demonstrate further the strong ligand field perturbation by an axial fluoride ligand.The five-coordinate fluoroiron(II) porphyrin complex also exhibits unique reactivity with dioxygen, in that the detectable products at ambient temperature are the peroxoiron(III) porphyrin and the difluoroiron(III) porphyrin anionic complexes.This observation is in contrast to the usual dioxygen conversion of simple iron(II) porphyrins to the dinuclear oxo-bridged iron(III) porphyrin.

Synthetic model approach to the active site of cytochrome c Oxidase: Studies of a heterodinuclear iron(III) porphyrin-copper(II) tripeptide complex

Elliott, C. Michael,Jain, Nemi C.,Cranmer, Brian K.,Hamburg, Arlene W.

, p. 3655 - 3659 (2008/10/08)

The reaction in THF of iron(II) meso-tetraphenylporphyrin, FeIITPP, with CuIII(aib3), where aib3 is the tripeptide of α-amino-isobutyric acid, results in the formation of a neutral heterodinuclear complex, [FeIII(TPP)CuII(aib3)] (1). Optical, conductance, electrochemical, magnetic, EPR, and Mo?ssbauer data are reported for the dinuclear complex 1. Isosbestic behavior is exhibited at 600, 525, and 415 nm by solutions of FeIITPP to which varying amounts of CuIII(aib3) are added, indicating the formation of 1. EPR and Mo?ssbauer spectra provide evidence for the presence of a high-spin (S = 5/2) iron(III) and (S = 1/2) copper(II) in complex 1. A weak antiferromagnetic interaction between the iron and copper is evident from the EPR measurements. While the magnetic interaction is weak, electrochemical and conductometric results indicate that the anionic CuII(aib3)- complex is moderately strongly bound to the FeIIITPP+.

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