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9-(4-phenylphenyl)fluorene

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Identification
Molecular formula
C25H16
CAS number
30759-91-0
IUPAC name
9-(4-phenylphenyl)-9H-fluorene
State
State

At room temperature, 9-(4-phenylphenyl)-9H-fluorene is in a solid state. It is stable under normal conditions of use and storage.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
476.50
Boiling point (Kelvin)
749.65
General information
Molecular weight
320.41g/mol
Molar mass
320.4050g/mol
Density
1.1842g/cm3
Appearence

9-(4-phenylphenyl)-9H-fluorene typically appears as a white to off-white crystalline powder. Its structural complexity gives it a rigid, three-dimensional shape which is characteristic of aromatic hydrocarbons.

Comment on solubility

Solubility of 9-(4-phenylphenyl)-9H-fluorene

9-(4-phenylphenyl)-9H-fluorene, a polycyclic aromatic hydrocarbon, exhibits specific solubility characteristics that are influenced by its molecular structure. Understanding its solubility can be nuanced, and here are some key points to consider:

  • Solvent Polarity: This compound is generally insoluble in polar solvents such as water due to its large hydrophobic aromatic framework.
  • Non-Polar Solvents: It displays good solubility in non-polar or weakly polar organic solvents like benzene, toluene, and chloroform.
  • Temperature Dependence: Solubility may increase with temperature in organic solvents, making it potentially useful in certain thermal applications.
  • Structural Influence: The presence of phenyl groups enhances π-π stacking interactions, which may slightly affect solubility characteristics in mixed solvent systems.

In summary, 9-(4-phenylphenyl)-9H-fluorene is primarily soluble in non-polar organic solvents while remaining largely insoluble in polar environments. This property can greatly influence its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about 9-(4-phenylphenyl)-9H-fluorene

9-(4-phenylphenyl)-9H-fluorene is a fascinating compound that belongs to the class of organics known as fluorene derivatives. It showcases some unique properties and applications that make it noteworthy in the field of chemistry.

Key Features and Applications

  • Fluorescent Properties: This compound exhibits strong fluorescence, which is essential for various applications in organic light-emitting diodes (OLEDs) and fluorescent labeling.
  • Structural Diversity: The presence of multiple phenyl groups in its structure provides it with enhanced stability and potentially interesting electronic properties.
  • Material Science: Due to its photophysical properties, 9-(4-phenylphenyl)-9H-fluorene is studied for its use in developing advanced materials with specific optical characteristics.
  • Research Interest: Chemists are exploring this compound's potential in fields such as photonics and organic semiconductors, where manipulating light-absorbing and emitting behaviors is crucial.

In the Laboratory

Researchers often delve into the synthesis and modification of 9-(4-phenylphenyl)-9H-fluorene to enhance its properties. Its unique structure allows for:

  • Modification of electronic properties, which can lead to the development of new materials with tailored functionalities.
  • Study of charge transport mechanisms that are vital in understanding and designing next-generation electronic devices.

Why It Matters

Understanding compounds like 9-(4-phenylphenyl)-9H-fluorene expands our knowledge of organic chemistry and its practical applications in technology. Its combination of fluorescent properties and structural complexity presents endless possibilities for innovation.

In the words of a notable chemist, "The future of technology lies in our ability to manipulate organic compounds to achieve desired functionalities."

Synonyms
9-(4-phenylphenyl)-9H-fluorene
17165-86-5
9-(1,1'-BIPHENYL)-4-YL-9H-FLUORENE
9-(1,1/'-Biphenyl)-4-yl-9H-fluorene
SCHEMBL27372447
SCHEMBL27658287
DTXSID40169145