133253-56-2

Usage

Uses

Used in Organic Chemistry:
Ethanedione, bis(2-nitrophenyl)is used as a reagent in organic chemistry for the synthesis of heterocyclic compounds and pharmaceuticals. Its unique structure and properties make it a valuable component in the development of various organic compounds.
Used in Colorimetric Analysis:
Ethanedione, bis(2-nitrophenyl)is used as a colorimetric reagent for the determination of various metals. Its ability to react with metals and produce color changes allows for the accurate measurement and identification of metal concentrations in different samples.
Used in Plastics and Polymers Industry:
Ethanedione, bis(2-nitrophenyl)is used as a stabilizer in plastics and polymers. Its presence helps to prevent the degradation of these materials, thereby enhancing their durability and performance.
Safety Precautions:
It is important to handle Ethanedione, bis(2-nitrophenyl)with care, as it is a toxic compound. Exposure to it may cause irritation to the skin, eyes, and respiratory system. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize the risk of adverse effects.

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 25407-11-8 1,2-bis(2-nitrophenyl)ethyne 
• 134-81-6 benzil 
• 59163-44-9 2-hydroxy-1,2-bis(2-nitrophenyl)ethanone 
• 7697-37-2 nitric acid 
• 7664-93-9 sulfuric acid 
• 35010-10-7 1-(2-nitrophenyl)-2-phenylethane-1,2-dione 
• 609-73-4 o-nitroiodobenzene 
• 577-19-5 2-nitrophenyl bromide 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 75867-47-9 trimethyl((2-nitrophenyl)ethynyl)silane 
• 16433-96-8 2-ethynyl-1-nitrobenzene 
• 64-19-7 acetic acid 
• 16968-19-7 2,2'-dinitrobibenzyl 

Downstream Products

• 3682-85-7 5,10-dihydroindolo<3,2-b>indole 
• 92060-45-2 2-(2-amino-phenyl)-indol-3-one 
• 1189192-81-1 5,5-bis(2-nitrophenyl)imidazolidine-2,4-dione 
• 1314030-09-5 5,5-bis(2-nitrophenyl)-2-thioxoimidazolidin-4-one 
• 1345622-25-4 C₄₁H₂₇N₅ 
• 1345622-28-7 C₃₅H₂₃N₅ 

Relevant academic research and scientific papers

Solution processed bulk heterojunction solar cells based on A-D-A small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups

Four acceptor-donor-acceptor (A-D-A) small molecules with dihydroindoloindole (DINI) as the central donor unit and different acceptor end groups such as dicyanovinylene (DCV), indenedione (IND), cyanoacrylate (CA) and rhodanine (Rho) linked through bithiophene as the π-linker, DINI-DCV, DINI-IND, DINI-CA and DINI-Rho, were designed and synthesized for the application as donor materials along with PC71BM as an acceptor for solution processed organic bulk heterojunction solar cells. The effect of acceptor end groups on the photovoltaic performance was investigated. The organic solar cells (OSCs) based on as cast DINI-IND showed the highest power conversion efficiency of 3.04%, as cast DINI-CA showed the lowest PCE of 1.63% and the other two exhibit a PCE in between them. These results showed that acceptor end groups affect the overall performance of the cells. The PCE of OSCs has been further improved up to 7.04% and 6.16% employing two-step annealing (TSA) treated DIN-IND:PC71BM (1:2) and DIN-CN:PC71BM (1:2), respectively. The enhancement in the PCE of OSCs with TSA treated active layers is attributed to the better nanophase morphology, the increase in the crystalline nature and light harvesting efficiency and more balanced charge transport and charge collection probability.

Synthesis and Characterization of Indolo[3,2-b]indole Based Copolymers for Bulk Heterojunction Polymer Solar Cell

A series of donor-acceptor low band gap polymers (DINIBT-C8, DINIBT-C10 and DINIBT-EH) containing 5,10-dihydroindolo[3,2-b]indole (DINI) as an electron donating unit and benzothiadiazole (BT) as an electron accepting unit with various kinds of alkyl chain

Double anchor indolo[3,2-: B] indole-derived metal-free dyes with extra electron donors as efficient sensitizers for dye-sensitized solar cells

Two new di-acceptors metal-free organic dyes based on indolo[3,2-b]indole donor backbone with extra electron donors were designed, synthesized, and applied for dye-sensitized solar cells (DSSCs). In this study, the effect of the additional donors was inve

5,10-dihydroindolo[3,2-b]indole-based copolymers with alternating donor and acceptor moieties for organic photovoltaics

A series of new donor-acceptor π-conjugated copolymers incorporating 5,10-dihydroindolo[3,2-b]indole (DINI) as an electron donating unit have been designed, synthesized, and explored in bulk heterojunction solar cells with diketopyrrolopyrrole and thienop

Dicyanovinyl-substituted indolo[3,2-b] indole derivatives: Low-band-gap π-conjugated molecules for a single-component ambipolar organic field-effect transistor

A series of low-band-gap π-conjugated molecules comprising N,N′-dihexylindolo[3,2-b]indole as an electron donor (D) and dicyanovinyl as an electron acceptor (A) with A-π-D-π-A architecture have been designed and synthesized to fabricate a single-component

Dipyrrole derivative and preparation method thereof as well as organic light-emitting device

The invention provides a dipyrrole derivative and a preparation method thereof as well as an organic light-emitting device and belongs to the technical field of organic optoelectronic materials. According to the dipyrrole derivative disclosed by the inven

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A heterocyclic compound and an organic light-emitting device including the heterocyclic compound, the heterocyclic compound being represented by Formula 1:

ELECTROACTIVE MATERIALS

There is disclosed a compound having Formula (I), Formula (II), Formula (III), Formula (VIII), Formula (IX), or Formula (X) The variables are described in detail in the application.

Compound and organic light-emitting device comprising the same

Provided are a compound of Formula 1 and an organic light-emitting device including the compound of Formula 1: The compounds of Formula 1 are particularly useful as fluorescent dopants in the emission layer of the organic light-emitting device.

Synthesis and characterization of new dihydroindolo[3,2-b]indole and 5,6-Bis(octyloxy)-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole-based polymer for bulk heterojunction polymer solar cells

We have designed and developed a new ladder type tetrafused π-conjugated building block such as dihydroindolo[3,2-b]indole (DINI) and investigated its role as an electron rich unit. The photovoltaic properties of a new semiconducting π-conjugated polymer,