457892-77-2

Basic information

• Product Name: N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide
• Synonyms: N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide
• CAS NO: 457892-77-2
• Molecular Weight: 912.179
• Mol File: 457892-77-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide(457892-77-2)
• EPA Substance Registry System: N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide(457892-77-2)

Safety Data

• Hazardous Substances Data: 457892-77-2(Hazardous Substances Data)

Upstream product

• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 104-75-6 2-Ethylhexylamine 
• 404871-21-2 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride 

Relevant articles and documents

Making a Molecular Wire: Charge and Spin Transport through para-Phenylene Oligomers

Functional molecular wires are essential for the development of molecular electronics. Charge transport through molecules occurs primarily by means of two mechanisms, coherent superexchange and incoherent charge hopping. Rates of charge transport through

ORGANIC COMPOUND, PHOTOVOLTAIC LAYER AND ORGANIC PHOTOVOLTAIC DEVICE

The present invention relates generally to the field of organic chemistry and particularly to the organic compound for organic photovoltaic devices. More specifically, the present invention is related to the organic compounds and the organic photovoltaic devices based on these compounds. In one preferred embodiment, this organic compound has the general structural formula (I) where Het1 is a predominantly planar polycyclic molecular system of first type; Het2 is a predominantly planar polycyclic molecular system of second type; A is a bridging group providing a lateral bond of the molecular system Het1 with the molecular system Het2 via strong chemical bonds; n is 1, 2, 3, 4, 5, 6, 7 or 8; B1 and B2 are binding groups; i is 0, 1, 2, 3, 4, 5, 6, 7 or 8; j is 0, 1, 2, 3, 4, 5, 6, 7 or 8; S1 and S2 are groups providing solubility of the organic compound; k is 0, 1, 2, 3, 4, 5, 6, 7 or 8; m is 0, 1, 2, 3, 4, 5, 6, 7 or 8; D1 and D2 are substituents independently selected from a list comprising -CH3, -C2H5, -NO2, -Cl, -Br, -F, - CF3, -CN, -OH, -OCH3, -OC2H5, -OCOCH3, -OCN, -SCN -NH2, -NHCOCH3, -C2Si(CH3)3, and -CONH2; y is 0, 1, 2, 3, 4, 5, 6, 7 or 8; and z is 0, 1, 2, 3, 4, 5, 6, 7 or 8. Said organic compound absorbs electromagnetic radiation in at least one predetermined spectral subrange within a wavelength range from 400 to 3000 nm and is capable to form supramolecules. The molecular system Het1, the bridging group A, and the molecular system Het2 are capable to form a donor - bridge - acceptor system providing dissociation of excited electron-hole pairs. A solution of the organic compound or its salt is capable of forming a solid photovoltaic layer on a substrate.

Charge transport in photofunctional nanoparticles self-assembled from zinc 5,10,15,20-tetrakis(perylenediimide)porphyrin building blocks

Molecules designed to carry out photochemical energy conversion typically employ several sequential electron transfers, as do photosynthetic proteins. Yet, these molecules typically do not achieve the extensive charge transport characteristic of semicondu