1282518-74-4

Usage

Molecular structure

2,5-dibutyl-3,6-bis(4'-formylphenyl)pyrrolo[3,4-c]pyrrole-1,4-dione has a complex molecular structure, which is a pyrrolopyrrole derivative containing two butyl groups and two formylphenyl groups.

Semiconducting properties

This chemical compound exhibits semiconducting properties, making it suitable for use in organic electronic devices.

Building block for high charge carrier mobility materials

Due to its semiconducting nature, 2,5-dibutyl-3,6-bis(4'-formylphenyl)pyrrolo[3,4-c]pyrrole-1,4-dione can be used as a building block for constructing materials with high charge carrier mobility.

Potential use in organic photovoltaic cells

The compound has been studied for its potential use in the development of organic photovoltaic cells, which are devices that convert sunlight into electricity.

Optoelectronic applications

2,5-dibutyl-3,6-bis(4'-formylphenyl)pyrrolo[3,4-c]pyrrole-1,4-dione is also being researched for its potential use in other optoelectronic applications, which involve the interaction of light with electronic materials.

Ongoing research and evaluation

The exact properties and potential applications of 2,5-dibutyl-3,6-bis(4'-formylphenyl)pyrrolo[3,4-c]pyrrole-1,4-dione are still being researched and evaluated, as it is a relatively new compound in the field of organic electronics.

Upstream product

• 105-07-7 4-cyanobenzaldehyde 
• 66739-89-7 4-(1,3-dioxolan-2-yl)benzonitrile 
• 1282518-71-1 2,5-dibutyl-3,6-bis[4-(1,3-dioxolan-2-yl)phenyl]pyrrolo-[3,4-c]pyrrole-1,4-dione 

Downstream Products

• 1346149-57-2 C₃₄H₂₈N₆O₂ 

Relevant academic research and scientific papers

Pyrrole-pyrroledione-based derivative fluorescent probe and application thereof

The invention discloses a pyrrole-pyrrole-dione-based derivative as shown in the formula I. R Is selected from - CH. 3 . - (CH)2 )n CH3 , (CH)2 )m CH2 X, CH (CH)3 )su

Donor-acceptor covalent organic frameworks of nickel(ii) porphyrin for selective and efficient CO2reduction into CO

Donor-acceptor two-dimensional covalent organic frameworks, PD-COF-23 and PD-COF-23-Ni, are constructed and applied for selective CO2 reduction with CO conversion rates of 20.9 μmol g-1 h-1 and 40.0 μmol g-1 h-1, respectively, in the absence of any additional photosensitizers and noble metal co-catalysts within an operation time of 25 h. The multilayer nanosheet structure, efficient charge separation and transport, and internal reductive quenching cycle of the NiTAPP fragments of PD-COF-23-Ni result in its higher photocatalytic efficiency than that of PD-COF-23. This journal is

Two new colorimetric and ratiometric fluorescent probes based on diketopyrrolopyrrole (DPP) for detecting and imaging of mitochondrial SO2 derivatives in cancer cells

Two new fluorescent probes (DPP-FI/DPP-BI) based on diketopyrrolopyrrole (DPP) were designed and synthesized for colorimetric and ratiometric detection of SO2 derivatives. Both of them displayed obvious ratiometric changes with about 21 folds o

Colorimetric and ratiometric fluorescent chemosensor based on diketopyrrolopyrrole for selective detection of thiols: An experimental and theoretical study

A colorimetric and ratiometric fluorescent thiol probe was devised with diketopyrrolopyrrole (DPP) fluorophore. The probe gives absorption and emission at 523 and 666 nm, respectively. In the presence of thiols, such as cysteine, the absorption and emissi

Synthesis of novel diketopyrrolopyrrole-based luminophores showing crystallization-induced emission enhancement properties

A series of diketopyrrolopyrrole-based luminophores were synthesized and characterized. Their photoluminescent properties were affected significantly by the change of π-conjugated units and alkyl groups linked to the diketopyrrolopyrrole-ring. 2,5-Dialkyl