1353896-27-1

Basic information

• Product Name: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis(3-benzomienyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc (II)
• Synonyms: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis(3-benzomienyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc (II)
• CAS NO: 1353896-27-1
• Molecular Weight: 1014.73
• Mol File: 1353896-27-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis(3-benzomienyl)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(3-benzomienyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc (II)(1353896-27-1)
• EPA Substance Registry System: 10,20-bis(3,5-di-tert-butylphenyl)-5,15-bis(3-benzomienyl)porphyrinato(2-)-κN21,κN22,κN23,κN24 zinc (II)(1353896-27-1)

Safety Data

• Hazardous Substances Data: 1353896-27-1(Hazardous Substances Data)

Upstream product

• 215313-78-3 [5,15-dibromo-10,20-bis-(3,5-di-tert-butyphenyl)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.