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Phenanthrenediamine

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Identification
Molecular formula
C14H10N2
CAS number
716-02-5
IUPAC name
phenanthrene-9,10-diimine
State
State

At room temperature, phenanthrene-9,10-diimine is a solid. It is slightly soluble in water but can be more soluble in organic solvents due to its aromatic structure.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
194.24g/mol
Molar mass
194.2370g/mol
Density
1.0700g/cm3
Appearence

Phenanthrene-9,10-diimine typically appears as a light yellow solid. This compound, being a diamine, is less typically encountered than phenanthrene, which is a polycyclic aromatic hydrocarbon appearing as colorless crystalline scales with blue fluorescence.

Comment on solubility

Solubility of Phenanthrene-9,10-diimine (C14H10N2)

Pheanthrene-9,10-diimine is an intriguing compound when it comes to solubility. The solubility of organic compounds, especially those containing nitrogen, can often be influenced by their structural characteristics. In the case of phenanthrene-9,10-diimine, several factors impact its solubility:

  • Molecular structure: The conjugated double bonds in the aromatic system may lead to limited solubility in polar solvents.
  • Polarity: Phenanthrene-9,10-diimine is primarily non-polar, which may present challenges in dissolving it in polar solvents like water.
  • Solvent interactions: It is more likely to be soluble in organic solvents such as benzene or dichloromethane due to similar polarity characteristics.

In summary, while phenanthrene-9,10-diimine might exhibit low solubility in polar solvents, it holds better solubility potential in non-polar organic solvents. As with many compounds, the interplay of structure and solvent type is key in determining how a specific substance will behave in solution.

Interesting facts

Interesting Facts about Phenanthrene-9,10-diimine

Pheanthrene-9,10-diimine is a fascinating organic compound that belongs to the class of aromatic amines and polycyclic aromatic hydrocarbons. This compound has drawn significant interest within the scientific community due to its unique structural features and chemical properties. Here are some key highlights:

  • Structural Significance: Phenanthrene-9,10-diimine contains two imine functional groups that enhance its reactivity and ability to participate in various chemical reactions.
  • Quinonoid Character: The presence of the imine groups contributes to the compound's quinonoid character, which is crucial for its role in electronic and optical applications.
  • Biological Activity: Some studies indicate that phenanthrene derivatives, including phenanthrene-9,10-diimine, exhibit biological activity. This includes potential anti-cancer properties, making it an interesting candidate for pharmaceutical research.
  • Photochemical Properties: The compound can absorb light in the ultraviolet range, leading to interesting applications in photochemistry and materials science, particularly in designing organic light-emitting diodes (OLEDs).
  • Research Applications: Researchers are exploring the use of phenanthrene-9,10-diimine as a ligand in coordination chemistry, forming complexes that could be used in catalysis or as sensors in analytical chemistry.

As noted by scholars in the field, "The diverse properties of polycyclic aromatic compounds make them suitable for a broad range of applications." Therefore, the study of phenanthrene-9,10-diimine continues to inspire new research avenues and practical uses in the context of modern chemistry.

Synonyms
Phenanthrene-9,10-diimine
9,10-Phenanthrenediimine
5665-52-1
NSC684322
8K49MB8V38
NSC-684322
NSC 684322
UNII-8K49MB8V38
SCHEMBL3141116
CHEMBL1981091
9,10-phenanthrenequinone diimine
NCI60_030272