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4CzIPN

4CzIPN structure

4CzIPN 

structure
  • CAS No:

    1416881-52-1

  • Formula:

    C56H32N6

  • Chemical Name:

    4CzIPN

  • Synonyms:

    4CzIPN;(4r,6r)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile;2,4,5,6-Tetra-9H-carbazol-9-yl-1,3-benzenedicarbonitrile;2,4,5,6-Tetra(9H-carbazol-9-yl)isophthalonitrile;2,4,5,6-tetrakis(carbazol-9-yl)-1,3-dicyanobenzene;1,2,3,5-Tetrakis(carbazol-9-yl)-4,6-dicyanobenzene

  • Categories:

    Pharmaceutical Intermediates  >  Oled Material Intermediate

Description

4CzIPN is an organic compound that is widely used in the field of photosensitive materials due to its unique chemical structure and properties. This compound typically appears as a white to pale yellow solid and possesses excellent optical and electrical characteristics. Its optical properties allow it to perform exceptionally well in optoelectronic devices, such as organic light-emitting diodes (OLEDs) and solar cells, where 4CzIPN effectively absorbs and emits light, thereby enhancing device performance. Additionally, its electrical properties provide potential application value in semiconductor materials, enabling efficient charge transport and carrier mobility. Due to these outstanding characteristics, 4CzIPN is gaining significant attention in the field of optoelectronic materials, becoming a focal point for research and development.

4CzIPN Basic Attributes

788.89348

788.269

0

Characteristics

67.3

13.7

1.32±0.1 g/cm3(Predicted)

Safety Information

|Warning|H302 (33.33%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 3 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene

4CzIPN Use and Manufacturing

Methods of Manufacturing

480 mg (12.0 mmol) of 60percent sodium hydride was placed in a 100-mE three-neck flask, the interior of the flask was substituted with nitrogen, and 40 mE, of N, N-dimethylformamide was added thereto, followed by stirring. 1.67 g (10.0 mmol) of 9H-carbazole was added to the mixture, which was stirred under a nitrogen stream at room temperature for 30 minutes. Afier stirring, 400 mg (2.00 mmol) of tetrafluoroisophthalonitrile was added to the mixture, and the mixture was stirred under a nitrogen atmosphere at 60° C. for 10 hours. Afier stirring, 5.0 mE of water was added to the mixture, which was then stirred. Afier stirring, N, Ndimethylformamide was removed from the mixture. After the removal, 200 mE of water was added to the mixture, to which ultrasonic waves were applied. Afier the application, the mixture was suction-filtered to provide a solid mattet The resulting solid matter was purified by silica gel colunmchromatography. In the column chromatography, a mixed solvent of chloroform and hexane (1/5) was firstly used as a developing solvent, and then a mixed solvent of chloroform and hexane (1/2) was used as a developing solvent. The resulting fraction was concentrated to provide a solid matter, which was then recrystallized from a mixed solvent of acetone, and hexane, thereby providing a yellow powdered solid matter in a yield amount of 311 mg and a yield of19.7percent.

Uses

As a compound widely used in optoelectronic devices and organic photovoltaic materials, 4CzIPN is recognized for its exceptional photosensitive and luminescent properties, making it a valuable photosensitizer and luminescent material. This material plays a crucial role in the development of new electronic devices, particularly in areas such as organic light-emitting diodes (OLEDs) and organic solar cells. The unique properties of 4CzIPN provide significant advantages in improving the efficiency, stability, and lifespan of electronic devices, thereby offering strong support for the research and application of next-generation electronic products. With ongoing technological advancements and the emergence of new materials, the application prospects of 4CzIPN in optoelectronic devices and organic photovoltaic materials are expected to expand further, potentially driving innovation and development in electronic devices.

Computed Properties

Molecular Weight:788.9
XLogP3:13.7
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:788.26884505
Monoisotopic Mass:788.26884505
Topological Polar Surface Area:67.3
Heavy Atom Count:62
Complexity:1560
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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