Vanadyl octaethylporphine

Product Number: VOO534; CAS Number: 27860-55-5

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Vanadyl octaethylporphine 2,3,7,8,12,13,17,18-Octaethyl-21H,23H-porphine vanadium (IV) oxide CAS: 27860-55-5 MDL: MFCD00058868

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Sizes Available:  100 mg, 25o mg, 1 g, 5 g and larger sizes available

Molecular weight: 599.702 g/mol

Molecular Formula: C36H44N4OV                        

CAS Number: 27860-55-5

Storage: Store at room temperature, protect from light

Synonyms: [2,3,7,8,12,13,17,18-Octaethylporphyrinato(2-)-κ2N21,N23](oxo)vanadium,[2,3,7,8,12,13,17,18-Octaethylporphyrinato(2-)-κ2N21,N23](oxo)vanadium, [2,3,7,8,12,13,17,18-Octaethylporphyrinato(2-)-κ2N21,N23](oxo)vanadium, [2,3,7,8,12,13,17,18-Octaéthylporphyrineato(2-)-κ2N21,N23](oxo)vanadium, 27860-55-5, MFCD00058868, Vanadium, [2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphinato(2-)-κN21,κN23]oxo-, 2,3,7,8,12,13,17,18-Octaethyl-21H,23H-porphine vanadium (IV) oxide, 2,3,7,8,12,13,17,18-Octaethyl-21H,23H-porphine vanadium(IV) oxide, VANADIUM OCTAETHYLPORPHINE OXIDE, Vanadyl octaethylporphine

Field of Interest: Models for Geoporphyrins, Photophysics

Background: Vanadyl octaethylporphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals. Vanadyl octaethylporphine is often used as a model for Vanadyl Petroporphyrins.

References:

1.) Kandrashkin, et al. Light-Induced Electron Spin Polarization in Vanadyl Octaethylporphyrin:  I. Characterization of the Excited Quartet State. J. Phys. Chem. A 2006, 110, 31, 9607–9616. https://doi.org/10.1021/jp0620365

2.) Kandrashkin, et al. Light-Induced Electron Spin Polarization in Vanadyl Octaethylporphyrin:  II. Dynamics of the Excited States. J. Phys. Chem. A 2006, 110, 31, 9617–9626. https://doi.org/10.1021/jp062037x 

3.) Bonnett, et al. Chemistry of Vanadyl Porphyrins. Tetrahedron. Volume 34, Issue 3, 1978, Pages 379-385. https://doi.org/10.1016/S0040-4020(01)93596-3

4.) Miyake, et al. Scanning tunneling microscopy investigation of vanadyl and cobalt(II) octaethylporphyrin self-assembled monolayer arrays on graphite. Colloids and Surfaces A: Physicochemical and Engineering Aspects. Volumes 313–314, 1 February 2008, Pages 230-233. https://doi.org/10.1016/j.colsurfa.2007.05.073

5.) Chen, et al. Metal Porphyrin Adsorption onto Asphaltene in Pentane Solution: A Comparison between Vanadyl and Nickel Etioporphyrins. Energy Fuels 2017, 31, 4, 3592–3601.https://doi.org/10.1021/acs.energyfuels.6b03100

6.) Ghosh, et al. Axial Ligand Coordination in Sterically Strained Vanadyl Porphyrins: Synthesis, Structure, and Properties. Inorg. Chem. 2008, 47, 21, 9848–9856. https://doi.org/10.1021/ic800714w

7.) Mironov, N.A., Milordov, D.V., Abilova, G.R. et al. Methods for Studying Petroleum Porphyrins (Review). Pet. Chem. 59, 1077–1091 (2019). https://doi.org/10.1134/S0965544119100074

8.) Mandal, et al. Non-catalytic vanadium removal from vanadyl etioporphyrin (VO-EP) using a mixed solvent of supercritical water and toluene: A kinetic study. Fuel. Volume 92, Issue 1, February 2012, Pages 288-294. https://www.sciencedirect.com/science/article/abs/pii/S0016236111003991

Categories

Porphyrins

Functional Groups

Alkyl

Metal

Vanadium Porphyrins

Porphyrin Family

Metallo Porphyrins, Octaethyl Porphyrins

Porphyrin Substitution

Alkyl Substituted Porphyrins, Beta Substituted Porphyrins

Purity %

>95%

Molecular Formula

C36H44N4OV

Molecular Weight

599.7

CAS #

27860-55-5

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