meso-Tetra(4-tert-butylphenyl) Porphine

meso-Tetra(4-tert-butylphenyl) Porphine CAS: 110452-48-7 MDL: MFCD20502349

Molecular weight: 839.16 g/mol

Molecular Formula: C₆₀H₆₂N₄

CAS Number: 110452-48-7

Storage: Store at room temperature, protect from light.

Synonyms: 21H,23H-Porphine, 5,10,15,20-tetrakis[4-(1,1-dimethylethyl)phenyl]-, 5,10,15,20-Tetrakis(4-tert-butylphenyl)porphyrin, 5,10,15,20-Tetrakis[4-(2-methyl-2-propanyl)phenyl]porphyrin, 5,10,15,20-Tetrakis[4-(2-methyl-2-propanyl)phenyl]porphyrin, 5,10,15,20-Tétrakis[4-(2-méthyl-2-propanyl)phényl]porphyrine, 110452-48-7, 2,7,12,17-tetrakis(4-tert-butylphenyl)-21,22,23,24-tetraazapentacyclo[16.2.1.13,?.1?,11.113,1?]tetracosa-1,3,5,7,9,11(23),12,14,16,18(21),19-undecaene, 5,10,15,20-Tetrakis(4-(1,1-dimethylethyl)phenyl)-21H,23H-porphine, 5,10,15,20-Tetrakis(4-tert.-butylphenyl)porphyrin, meso-Tetra(4-tert-butylphenyl) Porphine, MFCD20502349

Fields of Interest: Synthetic Porphyrins

Background: meso-Tetra(4-tert-butylphenyl) Porphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals.

References:

1.) Richeter, et al. Synthesis and structural characterisation of the first N-heterocyclic carbene ligand fused to a porphyrin. Chemical Communications, 2007, # 21, p. 2148 – 2150. https://doi.org/10.1039/B704681B

2.) Samankumara, et al. Syntheses, structures, modification, and optical properties of meso-tetraaryl-2,3-dimethoxychlorin, and two isomeric meso-tetraaryl-2,3,12,13- tetrahydroxybacteriochlorins. Organic and Biomolecular Chemistry, 2010, vol. 8, # 8, p. 1951 – 1965. https://doi.org/10.1039/B924539A

3.) Lefebvre, et al. Synthesis, characterization, and electronic properties of metalloporphyrins annulated to exocyclic imidazole and imidazolium rings. European Journal of Organic Chemistry, 2010, # 10, p. 1912 – 1920. https://doi.org/10.1002/ejoc.200901310

4.) Shi, et. al. Porphyrin-containing D-π-A conjugated polymer with absorption over the entire spectrum of visible light and its applications in solar cells. Journal of Materials Chemistry, 2012, vol. 22, # 22, p. 11006 – 11008. https://doi.org/10.1039/C2JM31649H

5.) Deshpande, et al. Opp-dibenzoporphyrins as a light-harvester for dye-sensitized solar cells. Chemistry – An Asian Journal, 2012, vol. 7, # 11, p. 2662 – 2669,8. https://doi.org/10.1002/asia.201200507

6.) Prakash, et al. Facile synthesis of β-functionalized “push-pull” Zn(II) porphyrins for DSSC applications. Dyes and Pigments, 2017, vol. 147, p. 56 – 66. https://doi.org/10.1016/j.dyepig.2017.07.053