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Acenaphthylene

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Identification
Molecular formula
C12H8
CAS number
208-96-8
IUPAC name
1,2-didehydro-1,2-dihydroacenaphthylene
State
State

At room temperature, acenaphthylene is in a solid state. It is a polycyclic aromatic hydrocarbon which tends to sublimate under certain conditions.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
279.00
Boiling point (Kelvin)
552.15
General information
Molecular weight
154.21g/mol
Molar mass
154.2070g/mol
Density
1.0240g/cm3
Appearence

Acenaphthylene appears as a pale yellow solid. It may come in the form of flakes or powder, depending on the method of preparation. At room temperature, it is typically stable but can emit an aromatic odor.

Comment on solubility

Solubility of 1,2-Didehydro-1,2-Dihydroacenaphthylene

1,2-Didehydro-1,2-dihydroacenaphthylene, a polycyclic aromatic hydrocarbon, showcases intriguing solubility characteristics due to its unique structure. In general, the solubility of such compounds can be influenced by several factors, including:

  • Polarity: Due to its nonpolar nature, 1,2-didehydro-1,2-dihydroacenaphthylene is primarily soluble in nonpolar solvents.
  • Temperature: Solubility often increases with temperature; therefore, heating the solvent may enhance the solubility of this compound.
  • Solvent Interaction: Compatible solvents such as toluene, benzene, or hexane can facilitate the dissolution process.

In essence, while 1,2-didehydro-1,2-dihydroacenaphthylene may exhibit limited solubility in polar solvents like water, it deeply engages with organic solvents. As always, *the key to effective solubility lies in the principle of "like dissolves like,"* emphasizing that similar polarities between solute and solvent lead to better solubility outcomes.

Interesting facts

Interesting Facts about 1,2-Didehydro-1,2-dihydroacenaphthylene

1,2-Didehydro-1,2-dihydroacenaphthylene is a fascinating compound in the field of organic chemistry, primarily known for its distinctive structure and intriguing properties. Here are some key points that highlight its significance:

  • Structural Characteristics: This compound features a unique arrangement of carbon atoms that allows for interesting reactivity patterns. The presence of double bonds introduces various electronic properties that chemists can exploit.
  • Isomeric Forms: 1,2-Didehydro-1,2-dihydroacenaphthylene has isomers that lead to different chemical behaviors and applications. Understanding these variations is crucial for chemists who are exploring potential uses in materials science.
  • Potential Applications: Compounds like 1,2-didehydro-1,2-dihydroacenaphthylene are often studied for their potential role in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
  • Reactivity: Given its structure, this compound exhibits intriguing reactivity under various conditions, allowing chemists to design experiments that can lead to novel derivatives with distinct properties.

As a student or scientist delving into the world of organic compounds, exploring 1,2-didehydro-1,2-dihydroacenaphthylene opens up discussions on structure-activity relationships, synthesis pathways, and the potential for creating new materials that could revolutionize technology. Studying this compound provides valuable insights into the fundamentals of organic chemistry and its applications in the modern world.