What is the chemical structure of 5,6,12,13-tetrachloro-2,9-bis [2,6-bis (isopropyl) phenyl] isoquinone [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetrone?

In the magical realm of chemistry, there is a wonderful combination of 5% 2C6% 2C12% 2C13, in which "% 2C" is the separator number, and this quaternary number should have its own unique relationship. Related to this, there is mention of "tetraalkane", and the number 2% 2C9. Furthermore, there is the peculiar expression "Bis [2% 2C6 - di (isobutyl) benzyl] heterosquare [4 ', 5', 6 ': 6, 5, 10] nitrile [2, 1, 9 - def] heterosquare light - 1, 3, 8, 10 (2H, 9H) ". This complex description refers to a delicate chemical structure.

This structure is the chemical structure of tetraether. In the tetraether structure, the connection of ether bonds forms a unique structure. In the partial view of "bi [2% 2C6-bis (isobutyl) benzyl]", a specific substituent isobutyl is attached to the benzyl group and distributed at positions 2 and 6. "Heteroscale [4 ', 5', 6 ': 6,5,10]" indicates the existence of a special spatial arrangement, or is determined by the stereoisomerism relationship. "Nitrile [2,1,9-def]" means that the nitrile group is in a specific position, as determined by the def numbering rule. "Light" in "Heteroscale - 1,3,8,10 (2H, 9H) " may imply a specific optical property, while 2H, 9H in parentheses indicate the location of a specific hydrogen atom. Overall, the complex and accurate description of this chemical structure reveals the unique chemical composition and spatial configuration of tetraether, which is of great significance and characteristics in the field of chemical research.

What are the physical properties of 5,6,12,13-tetrachloro-2,9-bis [2,6-bis (isopropyl) phenyl] isoquinone [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone?

"Tiangong Kaiwu" said: "The genus of Fu hardware has different qualities and properties. Yusi Siwu, 5% 2C6% 2C12% 2C13, is also four corners, its quality is firm and heavy, and its properties are stable and difficult to change. 2,9, Bis [2,6-di (isobutyl) benzyl] hetero [4 ', 5', 6 ': 6,5,10] blue [2,1,9-def] hetero-square light, with unique optical properties, or related to electron transition. 1,3,8,10 (2H, 9H) -tetrazine, its structure contains nitrogen heterocycles, so it has certain stability and reactivity.

The physical properties of these four substances, 5% 2C6% 2C12% 2C13, have high density, often have metallic luster, good thermal conductivity and electrical conductivity, and are mostly good conductors. Bis [2,6-di (isobutyl) benzyl] hetero [4 ', 5', 6 ': 6,5,10] blue [2,1,9-def] hetero-square light, under specific wavelengths of light, or show special color changes, with fluorescent or phosphorescent properties unknown. 1,3,8,10 (2H, 9H) -tetrazine, melting point and boiling point vary depending on intermolecular forces, and because of its nitrogen content, it may participate in many organic reactions, showing unique chemical activities, and may have potential applications in materials, medicine.

What are the chemical properties of 5,6,12,13-tetrachloro-2,9-bis [2,6-bis (isopropyl) phenyl] isoquinone [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9-def] isoquinoline-1,3,8,10 (2H, 9H) -tetraketone?

5% 2C6% 2C12% 2C13 refers to tetrayne, 2% 2C9 refers to bis [2% 2C6 - bis (isobutyl) phenyl] hetero [4 ', 5', 6 ': 6,5,10] nitrile [2% 2C1% 2C9 - def] isoplast - 1% 2C3% 2C8% 2C10 (2H% 2C9H) - tetrazine These compounds have some unique chemical properties.

These tetrazine compounds often have high nitrogen content, and the presence of nitrogen allows them to release more energy during combustion, thus having potential high energy density characteristics, which may have important applications in the field of energetic materials. From a structural point of view, its unique ring structure endows it with certain stability, but due to the functional groups at specific positions, the compound can undergo chemical reactions under appropriate conditions. For example, substitution reactions may occur with nucleophiles, because atoms or groups at certain positions have certain activities and are easily attacked and replaced by nucleophiles.

At the same time, such compounds may have good thermal stability and can maintain structural integrity within a certain temperature range, which is due to the strength of their chemical bonds and intermolecular forces. However, when the temperature exceeds a certain threshold, a decomposition reaction may be initiated, and gas products such as nitrogen may be released during the decomposition process. In addition, in organic synthesis, the tetrazine compound may be used as a key intermediate for the construction of more complex organic molecular structures, through the rational design of reaction pathways, using its special structure to introduce specific functional groups or build unique carbon-nitrogen skeletons.

5,6,12,13 - tetrachloro - 2,9 - bis [2,6 - bis (isopropyl) phenyl] isoquinone [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9 - def] isoquinoline - 1,3,8,10 (2H, 9H) - What are the application fields of tetrone?

5% 2C6% 2C12% 2C13 - tetranitrogen - 2% 2C9 - bis [2% 2C6 - bis (isobutyl) benzyl] hetero [4 ', 5', 6 ': 6% 2C5% 2C10] blue [2% 2C1% 2C9 - def] hetero - 1% 2C3% 2C8% 2C10 (2H% 2C9H) - tetrazine has a wide range of application fields.

In the field of materials science, due to its unique molecular structure and electronic properties, it can be used to create advanced materials with special optical and electrical properties. For example, it can be used as a luminescent material in organic Light Emitting Diode (OLED) technology to help improve the luminous efficiency and color performance of display devices; in the field of photovoltaic materials, it can enhance the capture and conversion efficiency of solar cells for light energy, and promote the development of renewable energy.

In the field of medicinal chemistry, tetrazine compounds show potential biological activity. They may be used as lead compounds, modified and optimized to develop new therapeutic drugs for the fight against tumors, inflammation and other diseases. Its special structure can interact with specific targets in the body to achieve precise treatment.

In organic synthetic chemistry, tetrazine is often used as a highly efficient reaction reagent. For example, in the construction process of some complex organic molecules, tetrazine can participate in the formation of specific chemical bonds, which provides an effective way for the synthesis of organic compounds with special structures and functions, and helps to expand the methodology of organic synthesis.

In supramolecular chemistry, tetrazine can build supramolecular systems by virtue of its own structure and other molecules through non-covalent interactions, such as hydrogen bonds 、π - π stacking. These supramolecular systems have important applications in the fields of molecular recognition, self-assembly, etc., and can be used to design intelligent responsive materials, molecular sensors, etc.

5,6,12,13 - tetrachloro - 2,9 - bis [2,6 - bis (isopropyl) phenyl] isoquinone [4 ', 5', 6 ': 6,5,10] anthracene [2,1,9 - def] isoquinoline - 1,3,8,10 (2H, 9H) - What is the preparation method of tetrone?

The tetraethers to be prepared are 5% 2C6% 2C12% 2C13 tetraalkane, 2% 2C9 bis, and [2% 2C6 isobutylbenzyl] hetero [4 '% 2C5'% 2C6 '% 3A6% 2C5% 2C10] blue [2% 2C1% 2C9 - def] hetero, and 1% 2C3% 2C8% 2C10 (2H% 2C9H). The preparation method is as follows:

First take an appropriate amount of 5% 2C6% 2C12% 2C13 tetraalkane and place it in a clean container. Then, add 2% 2C9 bis to it slowly in a certain proportion, and heat it with moderate temperature, and stir continuously to ensure that the two are fully blended.

After the two are mixed evenly, then add [2% 2C6 isobutylbenzyl] heterosquare [4 '% 2C5'% 2C6 '% 3A6% 2C5% 2C10] blue [2% 2C1% 2C9 - def] heterosquare light under appropriate conditions. During this process, pay attention to the regulation of temperature, and do not make the temperature too high or too low, so as not to affect the reaction process.

Finally, add 1% 2C3% 2C8% 2C10 (2H% 2C9H) in a timely manner, continue to stir and maintain a specific reaction time. After the reaction is completed, through a series of purification, separation and other processes, pure tetraether can be obtained. The whole process needs to be handled carefully, paying attention to the proportion, temperature and reaction time of each substance to obtain high-quality tetraether.