meso-Tetra (2-pyridyl) porphine

meso-Tetra (2-pyridyl) porphine 5,10,15,20-Tetra-2-pyridinyl-21H,23H-porphine CAS: 40904-90-3 MDL: MFCD00600954

SDS

Sizes Available:  100 mg, 1 g, 5 g, 10 g and larger sizes available

Molecular weight: 618.688 g/mol

Molecular Formula: C₄₀H₂₆N₈

CAS Number: 40904-90-3

Storage: Store at room temperature, protect from light

Synonyms: meso-Tetrakis(2-pyridyl)porphine, 21H,23H-Porphine, 5,10,15,20-tetra-2-pyridinyl- , 40904-90-3, 5,10,15,20-Tetra(2-pyridinyl)porphyrin,  5,10,15,20-Tetra(2-pyridinyl)porphyrin, 5,10,15,20-Tétra(2-pyridinyl)porphyrine, meso-Tetrakis(2-pyridyl)porphine, MFCD00600954, 2,7,12,17-TETRA(2-PYRIDINYL)-21,22,23,24-TETRAAZAPENTACYCLO[16.2.1.1(3,6).1(8,11).1(13,16)]TETRACOSA-1,3,5,7,9,11(23),12,14,16,18(21),19-UNDECAENE, 5,10,15,20-tetra(pyridin-2-yl)porphyrin, 5,10,15,20-tetra(pyridyl)porphyrin, 5,10,15,20-Tetra-2-pyridinyl-21H,23H-porphine, 5,10,15,20-Tetra-2-pyridylporphine, 5,10,15,20-Tetrakis(2-pyridyl)porphyrin, 5,10,15,20-Tetrakis(2-pyridyl)porphyrine, 5,10,15,20-Tetrapyridinylporphyrin, 5,10,15,20-tetrapyridylporphine, 5,10,15,20-tetrapyridylporphyrin, meso-Tetra (2-pyridyl) porphine, meso-Tetra (2-pyridyl)porphine, meso-Tetra(2-pyridyl)porphine, MFCD27978539, tetrapyridylporphyrin

Field of Interest: Synthetic Porphyrins, Water Soluble Porphyrins, Supramolecular Chemistry

Background: meso-Tetra (2-pyridyl) porphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals.

References:

1.) Nakazawa, et al. Encapsulation of Small Molecules by a Cavitand Porphyrin Self-Assembled via Quadruple Hydrogen Bonds. Org. Lett. 2006, 8, 19, 4275–4278. https://doi.org/10.1021/ol061561j

2.) Zakavi, et al. Effects of Core and/or Peripheral Protonation of meso-Tetra(2-, 3-, and 4-pyridyl)Porphyrin and meso-Tetra(3-methylpyridyl)Porphyrin on Their UV-vis Spectra. Journal of Spectroscopy. Volume 2013 Article ID 713745  https://doi.org/10.1155/2013/713745

3.) Neri, et al. Electrochemical reduction of some tetrapyridylporphines. Anal. Chem. 1973, 45, 3, 442–445. https://doi.org/10.1021/ac60325a011

4.) Matson, et al. Distant protonated pyridine groups in water-soluble iron porphyrin electrocatalysts promote selective oxygen reduction to water. Chem. Commun., 2012,48, 11100-11102. https://doi.org/10.1039/C2CC35576K

5.) De Luca, et al. Role of Counteranions in Acid-Induced Aggregation of Isomeric Tetrapyridylporphyrins in Organic Solvents. J. Phys. Chem. B 2005, 109, 15, 7149–7158. https://doi.org/10.1021/jp0448797

6.) Drain, et al. Self-Organized Porphyrinic Materials. Chem. Rev. 2009, 109, 5, 1630–1658. https://doi.org/10.1021/cr8002483