Skip to main content

1-Phenylphenanthrene

ADVERTISEMENT
Identification
Molecular formula
C20H14
CAS number
203-80-5
IUPAC name
1-phenylphenanthrene
State
State

At room temperature, 1-Phenylphenanthrene is a solid. The crystalline nature of the compound is due to the stacked arrangement of its planar aromatic molecules, enhancing its solid-state stability.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
464.00
Boiling point (Kelvin)
737.15
General information
Molecular weight
254.34g/mol
Molar mass
254.3390g/mol
Density
1.1290g/cm3
Appearence

1-Phenylphenanthrene appears as white to off-white crystalline solid. It is an aromatic hydrocarbon and displays a crystalline structure typical of such aromatic compounds.

Comment on solubility

Solubility of 1-phenylphenanthrene

1-phenylphenanthrene, with its aromatic structures, exhibits particular solubility characteristics that are noteworthy. Its solubility can be influenced by several factors:

  • Solvent Polarity: Being largely non-polar due to its extensive aromatic system, 1-phenylphenanthrene tends to dissolve better in non-polar organic solvents such as hexane, benzene, and toluene.
  • Temperature: Increased temperature often enhances solubility for many organic compounds, including 1-phenylphenanthrene, as higher kinetic energy can help overcome intermolecular forces.
  • Presence of Functional Groups: While 1-phenylphenanthrene lacks polar functional groups, the presence of other polar substituents in related compounds can significantly alter solubility behavior.

In conclusion, it is important to remember that the solubility of 1-phenylphenanthrene is generally limited in polar solvents such as water, making it a compound predominantly soluble in hydrophobic environments. Consequently, its behavior in solution will mostly exhibit trends characteristic of non-polar aromatic compounds.

Interesting facts

Interesting Facts About 1-Phenylphenanthrene

1-Phenylphenanthrene is an intriguing compound that belongs to the family of polycyclic aromatic hydrocarbons (PAHs). Often studied for its unique structure and properties, this compound offers a plethora of insights:

  • Structural Significance: The compound consists of a phenyl group attached to a phenanthrene skeleton, which is a fused three-ring aromatic system. This unique arrangement contributes to its stability and reactivity.
  • Fluorescent Properties: 1-Phenylphenanthrene exhibits notable fluorescence, making it a subject of interest in photophysical studies and applications in organic light-emitting diodes (OLEDs).
  • Environmental Impact: As a member of the PAH family, it is essential to consider the environmental implications of 1-phenylphenanthrene. Some PAHs are known to be carcinogenic, highlighting the need for careful handling and study in environmental science.
  • Chemical Transformations: This compound is often utilized in research to understand chemical transformations, such as electrophilic substitutions, due to its reactive aromatic system.
  • Potential Applications: Beyond its scientific curiosity, 1-phenylphenanthrene can potentially be exploited in materials science, particularly in the development of new organic materials that possess desirable photophysical properties.

In scientific literature, compounds like 1-phenylphenanthrene are often described using phrases like "the bridge between classical chemistry and modern applications," showcasing its role in advancing our understanding of organic compounds. Researchers continue to explore its properties and applications, making it a stimulating topic in the field of chemistry.

Synonyms
1-PHENYLPHENANTHRENE
Phenanthrene, 1-phenyl-
4325-76-2
DTXSID4075247
DTXCID5040251
rklromdzxdqsdf-uhfffaoysa-n
phenylphenanthrene
-Phenyl phenanthrene
AB-131/42301021