404871-21-2

Basic information

• Product Name: 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride
• Synonyms: 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride
• CAS NO: 404871-21-2
• Molecular Weight: 800.948
• Mol File: 404871-21-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride(CAS DataBase Reference)
• NIST Chemistry Reference: 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride(404871-21-2)
• EPA Substance Registry System: 1,7-(3’,5‘-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxydianhydride(404871-21-2)

Safety Data

• Hazardous Substances Data: 404871-21-2(Hazardous Substances Data)

Upstream product

• 1138-52-9 3,5-Di-tert-butylphenol 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 118129-60-5 1,7-dibromoperylene-3,4,9,10-tetracarboxylic dianhydride 

Downstream Products

• 768369-46-6 N'-(N,N-diethylaminophenyl)perylene-3,4-dicarboximide-9,10-dicarboxyanhydride 
• 404871-22-3 C₅₈H₅₉NO₇ 
• 457892-77-2 N-(2-ethylhexyl)-1,7-(3’,5’-di-t-butylphenoxy)perylene-3,4-dicarboxyanhydride-9,10-dicarboximide 
• 1185354-53-3 C₉₀H₉₂BrNO₇ 
• 1161933-75-0 C₇₆H₆₀N₄O₁₀ 
• 1207325-30-1 C₁₂₈H₁₁₄N₁₀O₁₄ 
• 1161933-80-7 C₁₈₀H₁₅₆N₈O₂₂ 
• 1161933-73-8 C₁₈₀H₁₇₈N₆O₁₈ 
• 865152-40-5 N-(1-ethylpropyl)-1,7-bis(3,5-di-tert-butylphenoxy)perylenedicarboxylic-3,4-anhydride 9,10-imide 
• 876301-65-4 5,12-bis-(3,5-di-tert-butyl-phenoxy)-2,9-bis-(2-ethyl-hexyl)-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 

Relevant articles and documents

ENERGY STORAGE MOLECULAR MATERIAL, CRYSTAL DIELECTRIC LAYER AND CAPACITOR

The present disclosure provides an energy storage molecular material, crystal dielectric layer and capacitor which may solve a problem of the further increase of volumetric and mass density of reserved energy associated with some energy storage devices, and at the same time reduce cost of materials.

Rigid oligoperylenediimide rods: Anion-π slides with photosynthetic activity

(Chemical Equation Presented) Slide rules: A new class of membrane-active rigid-rod molecules comprising π-acidic, n-semiconducting oligoperylene-diimides is introduced (see picture). They are able to combine passive anion transport across lipid bilayers with photoactive electron transport in the other direction across intact vesicle membranes. Thus, the compounds demonstrate artificial photosynthetic activity.

Self-assembly of supramolecular light-harvesting arrays from covalent multi-chromophore perylene-3,4:9,10=bis(dicarboximide) building blocks

We report on two multi-chromophore building blocks that self-assemble in solution and on surfaces into supramolecular light-harvesting arrays. Each building block is based on perylene-3,4:9,10-bis(dicarboximide) (PDI) chromophores. In one building block, N-phenyl PDI chromophores are attached at their para positions to both nitrogens and the 3 and 6 carbons of pyromellitimide to form a cross-shaped molecule (PI-PDI4). In the second building block, N-phenyl PDI chromophores are attached at their para positions to both nitrogens and the 1 and 7 carbons of a fifth PDI to produce a saddle-shaped molecule (PDI5). These molecules self-assemble into partially ordered dimeric structures (PI-PDI4)2 and (PDI5)2 in toluene and 2-methyltetrahydrofuran solutions with the PDI molecules approximately parallel to one another primarily due to π-π interactions between adjacent PDI chromophores. On hydrophobic surfaces, PDI5 grows into rod-shaped nanostructures of average length 130 nm as revealed by atomic force microscopy. Photoexcitation of these supramolecular dimers in solution gives direct evidence of strong π-π interactions between the excited PDI chromophore and other PDI molecules nearby based on the observed formation of an excimer-like state in 130 fs with a lifetime of about 20 ns. Multiple photoexcitations of the supramolecular dimers lead to fast singlet-singlet annihilation of the excimer-like state, which occurs with exciton hopping times of about 5 ps, which are comparable to those observed in photosynthetic light-harvesting proteins from green plants.