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8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene

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Identification
Molecular formula
C13H9I
CAS number
139882-14-7
IUPAC name
8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
State
State

At room temperature, this compound is typically a solid, often found as a crystalline powder. It has adequate stability under normal conditions but should be handled with care due to the presence of iodine, which can be reactive with certain substances.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
239.09g/mol
Molar mass
239.0890g/mol
Density
1.4800g/cm3
Appearence

8-Iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene is typically a crystalline solid that displays a striking golden yellow color. It often crystallizes well and can have a shiny or glossy finish. The compound, being an iodonium salt, will exhibit a certain level of ionic character, which may influence its crystalline structure.

Comment on solubility

Solubility of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene (C13H9I)

The solubility of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene, characterized by its unique structural arrangement, is an intriguing topic in the field of chemical science. This compound, containing an iodine atom, presents interesting interactions with solvents. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Solvents: Given its hydrocarbon nature with significant iodine presence, it is likely to show better solubility in nonpolar solvents such as hexane or toluene.
  • Influence of Iodine: The presence of the halogen may lead to some level of dipole-dipole interactions, potentially enhancing solubility in moderately polar solvents.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature, facilitating dissolution in various solvents.
  • Overall Behavior: The unique structure may contribute to a relatively low solubility in water due to the lack of polar functional groups that typically enhance water solubility.

In summary, the solubility characteristics of C13H9I are influenced by its molecular structure, the inherent properties of iodine, and the nature of interactions with various solvents. As with many organic halides, it demonstrates a preference for nonpolar environments.

Interesting facts

Interesting Facts About 8-Iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene

8-Iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene is a fascinating compound that belongs to the family of polycyclic aromatic hydrocarbons. Here are some interesting aspects that highlight its significance in the field of organic chemistry:

  • Structural Complexity: This compound features a unique and intricate structure consisting of multiple interlocking rings, making it a valuable subject for studying ring strain and molecular stability.
  • Role of Iodine: The presence of iodine not only influences the reactivity of the compound but also imparts interesting electronic properties. Iodine can play a crucial role in various reactions, including electrophilic substitutions.
  • Polycyclic Aromatic Hydrocarbons: As a member of this family, it shares characteristics with other well-known compounds like naphthalene and anthracene, which have applications in materials science and organic electronics.
  • Potential Applications: Due to its unique properties, this compound could have potential applications in organic synthesis and might serve as an intermediate in the development of pharmaceuticals and advanced materials.
  • Importance in Research: Compounds with intricate structures such as this one can help chemists understand fundamental concepts of molecular interactions, stability, and reactivity. As a result, they are often the focus of advanced research in synthetic organic chemistry.

As with many complex organic compounds, the study of 8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene opens doors to a deeper understanding of chemical structures and reactivity, leading to potential innovations in various fields.

Synonyms
Diphenyleneiodonium
Dibenziodolium
244-54-2
Diphenylene iodonium
2,2'-Biphenylyleneiodonium
dibenzo[b,d]iodolium
(1,1'-Biphenyl)-2,2'-diyliodonium
Dibenzo[b,d]iodol-5-ium
diphenyl-iodonium hydrochloride
CHEBI:77986
6HJ411TU98
8-iodoniatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaene
CHEMBL397686
UNII-6HJ411TU98
Tocris-0504
1010-76-0
Lopac-D-2926
Lopac0_000367
BSPBio_001027
KBioGR_000367
KBioSS_000367
SCHEMBL219548
CHEMBL365739
KBio2_000367
KBio2_002935
KBio2_005503
KBio3_000713
KBio3_000714
QFXKXRXFBRLLPQ-UHFFFAOYSA-
DTXSID00924595
Bio1_000428
Bio1_000917
Bio1_001406
Bio2_000344
Bio2_000824
HMS1362C09
HMS1792C09
HMS1990C09
HMS3403C09
BDBM50206334
CCG-204462
IDI1_002099
QTL1_000031
NCGC00015334-01
NCGC00015334-02
NCGC00015334-03
NCGC00015334-04
NCGC00015334-05
NCGC00015334-06
NCGC00015334-07
NCGC00015334-09
NCGC00015334-13
NCGC00024620-01
NCGC00024620-02
NCGC00024620-03
NCGC00024620-04
NS00015673
BRD-K65814004-001-02-3
BRD-K65814004-003-01-1
BRD-K65814004-003-02-9
Q27147567
InChI=1/C12H8I/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H/q+1