Pyrrolo[3,4-c]pyrrole-1,4-dione, 3,6-bis[3-(dodecylsulfonyl)phenyl]-2,5-dihydro-

The name of this compound is 3,6-bis [3- (dodecyl sulfonyl) phenyl] -2,5-dihydropyrrole [3,4-c] pyrrole-1,4-dione. Its chemical structure is as follows:
The core structure of this compound is pyrrole [3,4-c] pyrrole-1,4-dione, which is formed by fusing two pyrrole rings, and there is a carbonyl group (= O) attached at the 1st and 4th positions. It is in the dihydro form at the 2,5 positions, which means that these two positions are saturated, each with a hydrogen atom.
The key substituent is at the 3,6 position, all connected to 3- (dodecyl sulfonyl) phenyl. More specifically, a phenyl group is a six-membered aromatic ring with a dodecyl sulfonyl group attached to it at 3 positions. In the dodecyl sulfonyl group, the dodecyl group is an alkyl chain composed of twelve carbon atoms connected in a straight chain, and the sulfonyl group is the -SO ² - structure, which connects the dodecyl group to the phenyl group. In this way, two 3- (dodecyl sulfonyl) phenyl groups are respectively connected to the 3,6 positions of pyrrole and [3,4-c] pyrrole-1,4-dione, forming a unique chemical structure of the compound. The overall structure endows the compound with specific physical and chemical properties, which may exhibit unique properties in fields such as materials science.

This is 3,6-bis [3- (dodecyl sulfonyl) phenyl] -2,5-dihydropyrrole [3,4-c] pyrrole-1,4-dione, and its physical properties are unique and considerable.
Looking at its shape, under normal circumstances, this substance is mostly in the shape of a solid state, like a powder, with fine texture and often light color. However, the specific color may vary slightly depending on the preparation method and purity.
Talking about the melting point, after many experiments, its melting point is within a specific range. Due to the complexity of the molecular structure and the complex interactions between atoms, the molecule needs to obtain specific energy in order to break the lattice binding and convert from solid to liquid. The value of this melting point is one of its important physical properties, which can be used for discrimination and purity determination.
In terms of solubility, the performance of this substance in organic solvents is also worthy of attention. In some organic solvents, such as aromatics, halogenated hydrocarbons, etc., it exhibits a certain solubility. This is because the molecular structure contains specific groups, which interact with organic solvent molecules, such as van der Waals forces, hydrogen bonds, etc., to help it disperse in solvents. In water, its solubility is poor, because the hydrophobic part of the molecule accounts for a large proportion, and the force on water molecules is weak, making it difficult to melt in water.
In addition, the density of the substance is also a key physical property. The determination of density can help to understand the relationship between its mass and volume, and is of great significance in practical applications, such as preparation, process design, etc. The value of its density is closely related to the way of molecular stacking and atomic mass, and accurate determination can lay the foundation for subsequent research and application.
The 3,6-bis [3- (dodecyl sulfonyl) phenyl] -2,5-dihydropyrrolido [3,4-c] pyrrole-1,4-dione has rich and diverse physical properties, and each property is related to each other, which together affect its behavior and application in different scenarios.

This compound is called 3,6-bis [3- (dodecyl sulfonyl) phenyl] -2,5-dihydropyrrole [3,4-c] pyrrole-1,4-dione. Its main use, as far as is known today, involves the field of materials science.
In optoelectronic devices, this compound has outstanding performance. Because of its unique structure, excellent electron transport and optical properties, it is often the choice of organic Light Emitting Diode (OLED) materials. It can improve the luminous efficiency of OLED, make the luminous color purer, and help the display image quality to improve, which is of great significance to the development of high-end display technology.
In the field of solar cells, it also has its own shadow. It can be used as an active layer material to enhance the absorption and conversion efficiency of light. With the good photoelectric properties endowed by its own structure, it promotes the effective separation and transmission of electrons and holes, improves the photoelectric conversion efficiency of solar cells, and contributes to the utilization of renewable energy.
Furthermore, in the field of organic semiconductor materials, it can be used to prepare organic field effect transistors (OFETs). Due to its excellent electrical properties, it can improve the carrier mobility of OFETs, enhance the stability and performance of devices, and play a key role in the development of next-generation electronic devices. In short, this compound has important application value in many advanced materials and promotes the continuous innovation and progress of related technologies.

There is a method for the synthesis of 3,6 -bis [3 - (dodecyl sulfonyl) phenyl] -2,5 -dihydropyrrolido [3,4 - c] pyrrole-1,4 -dione, and let me tell you one by one.
First, the choice of raw materials is crucial. Choose a suitable 3- (dodecyl sulfonyl) benzene derivative, which is the key starting material, which needs to be of high purity and few impurities to make the reaction smooth. Its preparation also needs to be fine, such as reacting dodecyl sulfonyl chloride with benzene derivatives under suitable conditions to obtain the target 3- (dodecyl sulfonyl) benzene substance.
Second, build a pyrrole [3,4-c] pyrrole-1,4-dione skeleton. Often clever organic synthesis strategies, such as specific cyclization reactions. Nitrogen-containing and carbonyl-containing compounds can be used in the presence of catalysts, through a series of reactions such as condensation and cyclization, to gradually form the basic structure of pyrrole [3,4-c] pyrrole-1,4-dione. In this process, the type and dosage of catalysts, reaction temperature and time are all key factors. If the temperature is too high or too low, the reaction rate can be abnormal and the product is impure; if the time is not properly controlled, it is difficult to obtain the ideal yield.
Furthermore, 3- (dodecyl sulfonyl) phenyl is introduced into the 3,6 position of pyrrole [3,4-c] pyrrole-1,4-dione. This step can be achieved by coupling reaction. Appropriate coupling reagents and catalyst systems are selected to effectively connect the 3- (dodecyl sulfonyl) benzene derivative with the constructed pyrrole [3,4-c] pyrrole-1,4-dione intermediate. The reaction conditions need to be precisely regulated, and an anhydrous and oxygen-free environment may be necessary to prevent the growth of side reactions.
Furthermore, after the reaction is completed, the separation and purification of the product should not be underestimated. A variety of separation methods can be comprehensively used, such as column chromatography, according to the difference in the partition coefficient between the product and the impurity in the stationary phase and the mobile phase, to achieve the purpose of separation; recrystallization method, by the different solubility of the product and the impurity at different temperatures, purify the product. After these steps, careful operation can be obtained with high purity of 3,6-bis [3- (dodecyl sulfonyl) phenyl] -2,5-dihydropyrrole [3,4-c] pyrrole-1,4-dione.

Ugh! There is a product called Pyrrolo [3,4-c] pyrrole-1,4-dione, 3,6-bis [3- (dodecylsulfonyl) phenyl] -2,5-dihydro -. The application of this product is quite extensive.
In the field of materials, it can be used as a key component of special functional materials. Due to its unique molecular structure and specific photoelectric properties, it can be used to prepare high-performance organic optoelectronic devices. For example, Organic Light Emitting Diode (OLED) can help improve its luminous efficiency and stability, making the display screen clearer, brighter, and more realistic, contributing greatly to the development of display technology. < Br >
In the context of scientific research and exploration, it is an important research object. Chemists can deeply explore the relationship between molecular structure and properties by modifying its structure and properties, providing ideas and references for the design and synthesis of new compounds, and promoting knowledge expansion and innovation in the field of organic chemistry.
In biomedicine, although it has not been widely used, it may have potential biological activity due to its special structure. After in-depth research and development, it may be found in disease diagnosis, therapeutic drug research and development, etc., opening up new paths for human health.
In the field of energy storage, due to its special photoelectric properties, it may be used to develop new energy storage materials, such as high-performance battery electrode materials, to improve the charging and discharging efficiency and service life of batteries, which is of great significance for alleviating the energy crisis and promoting sustainable energy development.
From this perspective, Pyrrolo [3,4-c] pyrrole - 1,4-dione, 3,6-bis [3- (dodecylsulfonyl) phenyl] - 2,5-dihydro - has potential applications in many fields, and it is worth further research and development.