335654-34-7

Usage

Uses

Used in Inks and Coatings Industry:
N,N-dibutyl-5,6,12,13-tetrakis(4-(1,1-dimethylethyl)phenoxy)-3,4,9,10-perylenedicarboximide is used as a colorant in the inks and coatings industry for its high tinting strength and durability. Its excellent solubility and stability contribute to the production of vibrant and long-lasting colors in various applications.
Used in Plastics Industry:
In the plastics industry, N,N-dibutyl-5,6,12,13-tetrakis(4-(1,1-dimethylethyl)phenoxy)-3,4,9,10-perylenedicarboximide serves as a colorant, providing stable and vibrant colors to plastic products. Its high tinting strength and durability ensure that the color remains consistent and resistant to fading over time.
Used in Organic Electronic Devices:
N,N-dibutyl-5,6,12,13-tetrakis(4-(1,1-dimethylethyl)phenoxy)-3,4,9,10-perylenedicarboximide has been studied for potential use in organic electronic devices due to its favorable electronic properties. Its unique structure and properties make it a promising candidate for applications such as organic light-emitting diodes (OLEDs), organic solar cells, and other electronic devices that require high-performance materials.

Upstream product

• 98-54-4 para-tert-butylphenol 
• 95689-64-8 N,N’-dibutyl-1,6,7,12-tetrachloroperylene-3,4:9,10-tetracarboxylic acid bisimide 
• 156028-26-1 1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride 

Downstream Products

• 156028-30-7 1,6,7,12-tetrakis(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid dianhydride 
• 266678-68-6 N,N'-Di(4-pyridyl)-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid bisimide 
• 1026156-95-5 C₇₈H₈₃N₃O₁₀ 
• 335654-28-9 N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide 

Relevant academic research and scientific papers

NOVEL POLYHEDRAL OLIGOMERIC SILSESQUIOXANE (POSS) BASED FLUORESCENT COLORANTS

Novel fluorescent polyhedral oligomeric silsesquioxane (POSS) colorants are provided. The colorants are strongly fluorescing and long lasting with excellent light stability. The novel colorants can be prepared from chromophores found in common pigments an

Intramolecular energy transfer in a tetra-coumarin perylene system: Influence of solvent and bridging unit on electronic properties

The synthesis and characterisation of a novel coumarin donor-perylene bisimide acceptor light-harvesting system is reported, in which an energy-transfer efficiency of >99% is achieved. Comparison of the excited-state properties of the donor-acceptor syste

Synthesis of diazadibenzoperylenes and characterization of their structural, optical, redox, and coordination properties

Tetraphenoxy-substituted diazadibenzoperylenes 5a,b were synthesized from tetrachloroperylene tetracarboxylic acid bisanhydride 1 through imidization with benzylamine, nucleophilic displacement of the four chlorine atoms by phenolates, carbonyl group reduction by LiA1H4/A1C13, and subsequent Pd/C-promoted debenzylation-dehydrogenation. The structural properties of these extended diazaarenes are discussed on the basis of a X-ray crystal structure of the N,N'-dibutylated diazadibenzoperylenium dication 6, which revealed a 25° twist of the central six-membered ring leading to an atropisomeric π-conjugated backbone. The chromophoric systems of 5 and 6 were characterized by optical absorption and fluorescence spectroscopy, which revealed an intense fluorescence with a quantum yield of 75% for 5 and 50% for 6. Cyclic voltammetry showed reversible oxidation and reduction waves for 6, whereas the oxidation of 5 afforded the irreversible deposition of a conductive film on the electrode surface. Finally, the potential use of ligands 5 in supramolecular chemistry has been evaluated by complexation experiments with carboxylic acids and zinc tetraphenylporphyrin (ZnTPP).