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10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)

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  • Chemical Name:10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)
  • CAS No.:1246450-05-4
  • Molecular Formula:C64H60N4Zn
  • Molecular Weight:950.597
  • Hs Code.:
  • Mol file:1246450-05-4.mol
10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)

Synonyms:10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)

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Chemical Property of 10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II) Edit
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Technology Process of 10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)

There total 3 articles about 10,20-bis(3,5-di-tert-butylphenyl)-5-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
5,15-bis(3,5-di-tert-butylphenyl)porphyrin ZnII; With pyridine; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); In dichloromethane; at -10 - 0 ℃; for 0.25h; Reflux; Inert atmosphere;
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene; With pyridine; caesium carbonate; tetrakis(triphenylphosphine) palladium(0); In toluene; for 12h; Reflux; Inert atmosphere;
Guidance literature:
[5,15-bis-(3,5-di-tert-butylphenyl)porphyrinato]zinc(II); With N-Bromosuccinimide; sodium chloride; In pyridine; dichloromethane; at -10 - 0 ℃; Inert atmosphere;
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene; With tetrakis(triphenylphosphine) palladium(0); caesium carbonate; In toluene; at 110 ℃; for 12h; Inert atmosphere;
DOI:10.1002/anie.201002669
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