1246450-10-1

Basic information

• Product Name: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)
• Synonyms: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)
• CAS NO: 1246450-10-1
• Molecular Weight: 1150.84
• Mol File: 1246450-10-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)(CAS DataBase Reference)
• NIST Chemistry Reference: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)(1246450-10-1)
• EPA Substance Registry System: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis-(1-pyrenyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc(II)(1246450-10-1)

Safety Data

• Hazardous Substances Data: 1246450-10-1(Hazardous Substances Data)

Upstream product

• 215313-78-3 [10,20-bis-(3,5-di-tert-butylphenyl)-5,15-bis-bromoporphyrinato]zinc(II) 
• 349666-24-6 1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene 
• 187387-14-0 5,15-bis(3,5-di-tert-butylphenyl)porphyrin Zn^II 
• 215313-78-3 [5,15-dibromo-10,20-bis-(3,5-di-tert-butyphenyl)porphyrinato]zinc(II) 
• 294183-84-9 (5-bromo-10,20-bis(3,5-di-tert-butylphenyl)porphyrinato)zinc(II) 
• 187387-14-0 [5,15-bis-(3,5-di-tert-butylphenyl)porphyrinato]zinc(II) 

Downstream Products

• 1352088-84-6 [10-(3,5-di-tert-butylphenyl)-5,7,15,17-bis-(1,10-pyrendiyl)-porphyrinato]zinc(II) 
• 1352088-82-4 [10,20-bis-(3,5-di-tert-butylphenyl)-5,7,15,17-bis-(1,10-pyrendiyl)-porphyrinato]zinc(II) 

Relevant articles and documents

FUSING PORPHYRINS WITH POLYCYCLIC AROMATIC HYDROCARBONS AND HETEROCYCLES FOR OPTOELECTRIC APPLICATIONS

A compound that can be used as a donor material in organic photovoltaic devices comprising a non-activated porphyrin fused with one or more non-activated polycyclic aromatic rings or one or more non-activated heterocyclic rings can be obtained by a thermal fusion process. By heating the reaction mixture of non-activated porphyrins with non-activated polycyclic aromatic rings or heterocyclic rings to a fusion temperature and holding for a predetermined time, fusion of one or more polycyciic rings or heterocyclic rings to the non-activated porphyrin core in meso,β fashion is achieved resulting in hybrid structures containing a distorted porphyrin ring with annulated aromatic rings. The porphyrin core can be olygoporphyrins.

VISIBLE/NIR PHOTODETECTORS

Porphyrin compounds are provided. The compounds may further comprise a fused polycyclic aromatic hydrocarbon or a fused heterocyclic aromatic. Fused polycyclic aromatic hydrocarbon s and fused heterocyclic aromatics may extend and broaden absorption, and modify the solubility, crystallinity, and film-forming properties of the porphyrin compounds. Additionally, devices comprising porphyrin compounds are also provided. The porphyrin compounds may be used in a donor/acceptor configuration with compounds, such as C60.