96159-14-7

Upstream product

• 20541-49-5 bis(p-chlorophenyl) diselenide 
• 84632-65-5 3,6-bis(4-chlorophenyl)-2,5-dihydro-1,4-diketopyrrolo[3,4-c]pyrrole 
• 74-88-4 methyl iodide 

Downstream Products

• 1404233-88-0 C₄₀H₃₄N₄O₂ 
• 1404233-87-9 C₃₂H₁₄F₁₀N₂O₂ 
• 1404233-89-1 C₅₂H₃₄N₁₂O₂ 
• 1404233-86-8 C₃₂H₃₈B₂N₂O₆ 

Relevant academic research and scientific papers

Synthesis and characterization of dioxopyrrolopyrrole derivatives having electron-withdrawing groups

New dioxopyrrolopyrrole (DPP) derivatives bearing electron-withdrawing groups have been synthesized, and their photophysical properties and redox behaviors have been examined. The electron-accepting abilities of the derivatives were elucidated by cyclic voltammetry (CV) and redox titration analysis. The introduction of the electron-withdrawing groups modulated the redox properties of the DPP core, and the addition of the 1,1,4,4- tetracyanobutadiene (TCBD) moieties created a multi-redox system. The application of TD-DFT (time-dependent density functional theory) revealed the HOMO and LUMO of the compounds, and the calculation results were consistent with the photophysical and electrochemical properties of the compounds. The TCBD moieties provided the dye molecule with unique physical properties such as broad charge-transfer absorption bands and reversible multi-redox behavior. Copyright

Fluorescent diketopyrrolopyrroles

The present invention relates to fluorescent diketopyrrolopyrroles of formula I and processes for its preparation, its uses and compositions comprising the compounds of formula I.