What is the chemical structure of 2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone

The full name of this compound is long and the structure is complex. The following is your step-by-step analysis of its structure.

"2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisobenzofuran-1,3,8,10 (2H, 9H) -tetraketone". It can be seen from the name that the compound is based on anthracene as the core skeleton. The 2,9 positions in the anthracene structure are replaced by bis (3,5-dimethylphenyl), that is, a phenyl group containing two methyl groups (at the 3,5 positions) is connected to the 2,9 positions of the anthracycline, respectively. At the same time, anthracycline and two isobenzofuran-1,3,8,10 (2H, 9H) -tetraketone structures are connected by fusing, which involves [2,1,9-def: 6,5,10-d'e'f '] This specific fusing method is described, indicating the connection position and mode between the rings.

Overall, the compound structure contains multiple aromatic ring systems, including anthracycline, benzene ring and isobenzofuranone ring system. Its unique chemical structure is constructed through specific substitution and fusing methods, showing complex and highly conjugated characteristics of polycyclic aromatic hydrocarbon derivatives.

What are the physical properties of 2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone

2% 2C9-bis (3% 2C5-dimethylphenyl) naphthalene [2% 2C1% 2C9-def: 6% 2C5% 2C10-d'e'f '] diisoprene-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetrazine This compound has unique physical properties.

Its appearance may show a specific color and morphology. In terms of solubility, due to the presence of large aromatic groups in the structure of the compound, it may exhibit a certain solubility in common organic solvents such as toluene and dichloromethane. This is due to the principle of similar miscibility. The intermolecular force between its aromatic structure and the organic solvent prompts the dissolution process to occur.

From the point of view of melting point, the melting point is expected to be relatively high due to the strong π-π stacking and van der Waals force between molecules. This is because the closely arranged molecular structure requires higher energy to overcome the intermolecular forces, causing the lattice structure to disintegrate and undergo phase transition.

In terms of stability, due to the inclusion of multiple conjugate systems in the molecule, the conjugate effect can make the electron cloud distribution more uniform, thereby enhancing the stability of the compound. However, there may be certain reactivity check points in the diisoprene and tetrazine structures. Under certain conditions, such as strong oxidizing agents, reducing agents or high temperature environments, chemical reactions may occur, which may affect their stability. The optical properties of

are also quite interesting. Due to the existence of the conjugated system, the compound may have good fluorescence properties. Under the excitation of light, electrons transition in the conjugated system, and then emit specific wavelengths of fluorescence. It can be applied to fields such as fluorescent materials.

What are the application fields of 2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone

2% 2C9 -bis (3% 2C5 -dimethylphenyl) silicon [2% 2C1% 2C9 -def% 3A6% 2C5% 2C10 -d'e'f '] diisoprene-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone, this substance has a unique chemical structure and shows application potential in many fields.

In the field of organic synthesis, its complex and special molecular structure can be used as a key intermediate for the construction of more complex and novel organic compounds. With its specific electron cloud distribution and activity checking point, it can participate in a variety of organic reactions, such as nucleophilic substitution, electrophilic addition, etc., to help synthesize organic materials with special functions.

In the field of materials science, this substance may endow materials with unique electrical and optical properties due to its own rigid planar structure and the introduction of silicon atoms. It may be used to prepare high-performance optoelectronic materials, such as light-emitting layer materials in organic Light Emitting Diodes (OLEDs), which achieve efficient energy conversion and luminous efficiency due to their structural properties; or as active layer materials for field effect transistors (FETs), which exhibit unique carrier transport properties.

In the field of medicinal chemistry, its complex structure may provide new opportunities for drug research and development. By modifying its structure, compounds with specific biological activities can be designed to interact with specific targets in organisms, and new therapeutic drugs are expected to be developed, such as inhibitors of certain disease-related proteins.

In supramolecular chemistry, using its unique shape and electronic properties, it can be used as a host molecule to interact with suitable guest molecules through non-covalent interactions, such as hydrogen bonding 、π - π stacking, to form supramolecular assemblies and construct supramolecular systems with specific functions, which are applied in molecular recognition, catalysis and other fields.

In summary, 2% 2C9 -bis (3% 2C5 -dimethylphenyl) silicon [2% 2C1% 2C9 -def% 3A6% 2C5% 2C10 - d'e'f '] diisoprene-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone has potential applications in many fields such as organic synthesis, materials science, medicinal chemistry and supramolecular chemistry, providing new directions and possibilities for research and development in various fields.

What is the synthesis method of 2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone

2% 2C9 -bis (3% 2C5 -dimethylphenyl) naphthalene [2% 2C1% 2C9 - def% 3A6% 2C5% 2C10 - d'e'f '] diisoprene-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone is synthesized as follows:

First, a multi-step reaction is required to construct the naphthalene ring and connect the substituents such as dimethylphenyl. The choice of starting materials is crucial, and aromatic compounds with suitable activity check points can be selected.

First, the initial aromatic compound is halogenated at a specific position, and halogen atoms are introduced to facilitate subsequent nucleophilic substitution reactions. This step requires precise control of the reaction conditions, such as reaction temperature, solvent and catalyst, to ensure the selectivity of the halogenation position.

Subsequently, the halogenated product and the reagent containing dimethylphenyl are coupled under palladium catalysis and other conditions to form a connection structure between the naphthalene ring and dimethylphenyl. In this process, the type and dosage of palladium catalysts, the selection of ligands, etc., have a great impact on the reaction efficiency and selectivity.

Furthermore, the obtained intermediate is oxidized to construct the carbonyl structure in the target product. The conditions of the oxidation reaction need to be finely regulated. Different oxidizing agents, reaction temperatures, and times will affect the position and quantity of carbonyl formation.

After the above series of reactions, by gradually constructing the molecular structure, 2% 2C9-bis (3% 2C5-dimethylphenyl) naphthalene [2% 2C1% 2C9 - def% 3A6% 2C5% 2C10 - d'e'f '] diisoprene-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone can be obtained. After each step of the reaction, the products need to be separated and identified by chromatography, spectroscopy and other analytical methods to ensure that the reaction proceeds in the expected direction and obtain high-purity target products.

What is the market outlook for 2,9-bis (3,5-dimethylphenyl) anthracene [2,1,9-def: 6,5,10-d'e'f '] diisoquinoline-1,3,8,10 (2H, 9H) -tetraketone?

2% 2C9 -Bis (3% 2C5 -dimethylphenyl) naphthalene [2% 2C1% 2C9 -def: 6% 2C5% 2C10 -d'e'f '] diisobenzofuran-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone What is the market prospect of this substance? Let me answer you with the ancient saying of Tiangong Kaiwu.

The 2% 2C9-bis (3% 2C5-dimethylphenyl) naphthalene [2% 2C1% 2C9-def: 6% 2C5% 2C10-d'e'f '] diisobenzofuran-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone has promising prospects in various fields. In the field of materials, its unique molecular structure may give it specific optical and electrical properties. As "Tiangong Kaiwu" said, "All things in the world have their uses. If you are good at observing physical properties, you can do your best." This material may be used to create new types of optoelectronic materials to meet the urgent needs of high-performance materials in today's electronics, display and other industries.

Furthermore, on the road of scientific research and exploration, the novelty of its structure must lead scholars to explore its reaction mechanism and performance characteristics. This is just like the ancients who studied physical properties and exhausted their reasons to develop innovative methods. Through the deep cultivation of scientific research, more potential uses of it may be discovered, which will contribute to the development of materials science.

Although the market prospect is promising, many difficulties need to be taken into account. The method of preparation may need to be carefully controlled, and the cost is also related to the expansion of its market. Just like ancient skills, if you want to improve, you need to spend labor and time, and the cost will follow. Only by finding efficient and economical preparation methods can you stand out in the market competition. And it will take time for the market to accept new products. It needs to attract the attention of the industry and know its advantages in order to gradually enter the market and be widely used by people.

In summary, the market prospect of 2% 2C9-bis (3% 2C5-dimethylphenyl) naphthalene [2% 2C1% 2C9-def: 6% 2C5% 2C10-d'e'f '] diisobenzofuran-1% 2C3% 2C8% 2C10 (2H% 2C9H) -tetraketone, opportunities and challenges coexist. With time, good management and research and development may emerge and make achievements in materials and other fields.