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Diphenylhexatriene

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Identification
Molecular formula
C18H14
CAS number
1730-10-3
IUPAC name
6-phenylhexa-1,3,5-trienylbenzene
State
State

At room temperature, diphenylhexatriene exists as a crystalline solid. The solid has a distinct yellow color characteristic of compounds with conjugated double bond systems.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
379.30
Boiling point (Kelvin)
652.45
General information
Molecular weight
230.31g/mol
Molar mass
230.3100g/mol
Density
1.0337g/cm3
Appearence

Diphenylhexatriene is typically a yellow crystalline solid. It acquires this color due to the conjugated system extending over a series of double bonds, which participate in extensive delocalization of pi electrons. These characteristics contribute to its significant spectroscopic properties.

Comment on solubility

Solubility of 6-phenylhexa-1,3,5-trienylbenzene

6-phenylhexa-1,3,5-trienylbenzene, a compound characterized by its conjugated double bonds and aromatic system, exhibits some intriguing solubility properties:

  • Non-polar Solvents: This compound is primarily soluble in non-polar organic solvents due to its hydrophobic nature. Solvents such as hexane, toluene, and diethyl ether are often suitable for dissolving 6-phenylhexa-1,3,5-trienylbenzene.
  • Polar Solvents: Conversely, it demonstrates poor solubility in polar solvents like water or alcohols. This is attributed to the inability of these solvents to effectively interact with the non-polar regions of the molecule.
  • Temperature Dependence: The solubility can also be influenced by temperature. Generally, higher temperatures may enhance solubility in organic solvents due to increased molecular motion.
  • Applications: Understanding the solubility characteristics is crucial for utilizing this compound in various chemical reactions and formulations, particularly in organic synthesis and material science.

In summary, for optimal solubility of 6-phenylhexa-1,3,5-trienylbenzene, one should prioritize non-polar solvents while taking into account temperature adjustments to enhance dissolution.

Interesting facts

Interesting Facts About 6-phenylhexa-1,3,5-trienylbenzene

6-phenylhexa-1,3,5-trienylbenzene is a fascinating compound that belongs to the family of polycyclic aromatic hydrocarbons (PAHs). Its unique structure and properties open up diverse avenues for exploration:

  • Conjugation and Stability: This compound features a highly conjugated system with alternating double bonds, which enhances its stability and allows for interesting electronic properties.
  • Photophysical Properties: Due to its conjugated structure, 6-phenylhexa-1,3,5-trienylbenzene exhibits remarkable photophysical behavior, including fluorescence, making it a candidate for various photonic applications.
  • Applications in Organic Electronics: The compound's ability to conduct electricity due to its π-electron system makes it valuable in the development of organic semiconductors, sensors, and light-emitting diodes (LEDs).
  • Synthesis Pathways: Researchers have developed innovative synthetic strategies to create this compound, which often involves cross-coupling reactions and other modern organic synthesis techniques.

In summary, the study of 6-phenylhexa-1,3,5-trienylbenzene not only enriches our understanding of aromatic compounds but also paves the way for advancements in the fields of materials science and organic electronics. By investigating its properties, researchers can uncover potential new applications that might revolutionize technology.

Synonyms
DTXSID9061912
DTXCID8035502
6-phenylhexa-1,3,5-trienylbenzene
1,6-diphenyl-1,3,5-hextriene
BOBLSBAZCVBABY-UHFFFAOYSA-N
PD130242
NS00025641
(1E ,3E ,5E )-1,6-Diphenylhexa-1,3,5-triene