335654-28-9

Upstream product

• 109-73-9 N-butylamine 
• 156028-30-7 1,6,7,12-tetrakis(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid dianhydride 
• 335654-34-7 N,N'-dibutyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid bisimide 

Downstream Products

• 478491-50-8 2-butyl-5,6,12,13-tetrakis-(4-tert-butyl-phenoxy)-9-(4-[2,2';6',2'']terpyridin-4'-yl-phenyl)-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 
• 1196670-76-4 C₉₀H₁₀₀N₂O₈S₈ 
• 1411700-49-6 N-butyl-tetra(tert-butylphenoxy)methoxybenzo[c,d]perylenone 
• 1574527-41-5 C₈₂H₈₁N₅O₈ 
• 1400874-45-4 N-n-butyl-N-p-phenylenediamine-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic diimide 
• 1400874-43-2 C₁₀₆H₉₁N₅O₁₃ 
• 1259371-46-4 C₇₄H₇₀BF₂N₃O₇ 

Relevant academic research and scientific papers

Synthesis and properties of a covalently linked angular perylene imide dimer

Utilizing the unexplored chemistry of a monocarbon analog to perylene bisimide, a covalently linked angular perylene dimer was synthesized. On the basis of measured optical properties and molecular modeling, the spectral changes relative to a monomeric reference perylene can be explained by an angle-dependent oblique exciton coupling model. With a roughly trigonal interchromophore arrangement, the dimer building block is promising for larger, cyclic assemblies to mimic naturally occurring light harvesting complexes.

Highly soluble perylene tetracarboxylic diimides (PDI)-tetrathiafulvalene (TTF) dyad and TTF-PDI-TTF triad

(Chemical Equation Presented) Two highly soluble donor-σ-acceptor and donor-σ-accepter-σ-donor type fluorescence switches consisting tetrathiafulvalene (TTF) and 3,4,9,10-perylene tetracarboxylic diimides (PDI) were synthesized. The structure of the dyad

Tuning energy transfer in switchable donor-acceptor systems

The synthesis and characterisation of a coumarin-dithienylcyclopentene- coumarin symmetric triad (CSC) and a perylene bisimide-dithienylcyclopentene- coumarin asymmetric triad (PSC) are reported. In both triads the switching function of the photochromic dithienylcyclopentene unit is retained. For CSC an overall 50% quenching of the coumarin fluorescence is observed upon ring-closure of the dithienylcyclopentene component, which, taken together with the low PSS (a 60% decrease in sensitized perylene bisimide emission intensity is observed due to competitive quenching of the coumarin excited state and partial quenching of the perylene excited state by the closed dithienylcyclopentene unit. This modulation of energy transfer is reversible over several cycles for both the symmetric and asymmetric tri-component systems. The Royal Society of Chemistry.

Novel fluorescent dyes with fused perylene tetracarboxlic diimide and BODIPY analogue structures

(Chemical Equation) Two novel fluorescent dyes based on perylene tetracarboxylic diimides and BODIPY were designed and synthesized. Significant features, such as longer wavelength absorption and emission, high fluorescence quantum yields, and strong elect