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Triphenylarsine sulfide

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Identification
Molecular formula
C18H15AsS2
CAS number
637-13-2
IUPAC name
phenyl-bis(phenylsulfanyl)arsane
State
State
At room temperature, Triphenylarsine sulfide is in a solid state. It often appears as a powder with a slightly greasy feel.
Melting point (Celsius)
82.00
Melting point (Kelvin)
355.00
Boiling point (Celsius)
402.00
Boiling point (Kelvin)
675.00
General information
Molecular weight
400.49g/mol
Molar mass
400.4910g/mol
Density
1.4200g/cm3
Appearence

Triphenylarsine sulfide appears as a light yellow, crystalline powder. It has a characteristic odor and can exhibit a greasy or waxy texture due to its organoarsenic structure.

Comment on solubility

Solubility of Phenyl-bis(phenylsulfanyl)arsane

Pheynl-bis(phenylsulfanyl)arsane, with its complex structure, presents unique challenges in terms of its solubility properties. Overall, it is important to note the following characteristics:

  • Polarity: The compound's polar and non-polar groups can significantly affect its solubility in solvents.
  • Solvent Interaction: It may exhibit better solubility in non-polar organic solvents due to its phenyl groups.
  • Hydrogen Bonding: The potential for hydrogen bonding can influence solubility in polar solvents.
  • Concentration Effects: Increasing the concentration of phenyl-bis(phenylsulfanyl)arsane can reach saturation points, leading to precipitation in certain solvents.

In conclusion, while specific solubility data for phenyl-bis(phenylsulfanyl)arsane may be limited, the general trends associated with similar arsanic compounds suggest it is primarily soluble in non-polar organic environments. As always, the exact solubility can be influenced heavily by the presence of other solutes, impurities, and the specific conditions of the solution.

Interesting facts

Interesting Facts about Phenyl-bis(phenylsulfanyl)arsane

Packed with intriguing features, phenyl-bis(phenylsulfanyl)arsane showcases the fascinating chemistry of arsenic compounds. Below are some key points highlighting its significance and applications:

  • Organometallic Chemistry: This compound serves as a pivotal example in the field of organometallic chemistry, demonstrating how organosulfur and organoarsenic compounds can interact.
  • Structural Insights: The unique arrangement of sulfanyl groups and their attachment to a central arsenic atom underscore the compound’s structural complexity. Such architectures can lead to interesting electronic properties.
  • Potential Applications: With its dual phenylsulfanyl groups, this compound exhibits potential in various fields, including materials science and biomedical research. Functional groups of this nature often impart stability and reactivity that can be harnessed in synthesis.
  • Ligand Behavior: Phenyl-bis(phenylsulfanyl)arsane may act as a bidentate ligand in coordination chemistry, forming complexes with transition metals, thus serving vital roles in catalysis.
  • Health and Environmental Impact: As an organoarsenic compound, it is important to consider the health implications associated with arsenic. Understanding these compounds assists scientists in evaluating their environmental consequences.

Overall, phenyl-bis(phenylsulfanyl)arsane is not just another compound; it represents a blend of utility and risk that makes it a topic of keen interest for researchers and students alike. Its multifaceted nature encourages ongoing study in the realms of chemistry and materials.

Synonyms
DIPHENYL PHENYLARSONODITHIOATE
24582-59-0
DTXSID00179326