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Corannulene

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Identification
Molecular formula
C20H10
CAS number
191-55-3
IUPAC name
hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene
State
State

Corannulene at room temperature is a crystalline solid.

Melting point (Celsius)
268.00
Melting point (Kelvin)
541.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
300.36g/mol
Molar mass
300.3610g/mol
Density
1.9000g/cm3
Appearence

Corannulene is often encountered as crystalline solid having a yellow to orange appearance. It has a distinctive concave shape due to its bowl-like structure, which arises from the non-planar arrangement of five fused benzene rings.

Comment on solubility

Solubility of Hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene

Hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene is a fascinating compound, known for its complex structure and unique chemical properties. When considering its solubility, several key factors come into play:

  • Polarity: The solubility of a substance greatly depends on the polarity of the molecule. In general, like dissolves like, so polar compounds tend to dissolve well in polar solvents, while nonpolar compounds are more soluble in nonpolar solvents.
  • Structure: The intricate cyclic arrangement of hexacyclo-tetracosa contributes to its limited interaction with standard solvents. The compact nature of the compound results in a low likelihood of solvation.
  • Solvent Choice: This compound is expected to exhibit low solubility in common solvents such as water due to its nonpolar characteristics. However, it may demonstrate better solubility in nonpolar organic solvents like hexane or chloroform.
  • Temperature: As with many organic compounds, solubility may increase with temperature, making it important to consider thermal conditions when attempting to dissolve the compound.

In conclusion, the solubility of hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene is likely limited in polar environments but may find pathways to solubility in nonpolar solvents. Understanding these solubility dynamics is essential for researchers working with this intricate compound.

Interesting facts

Interesting Facts about Hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene

This complex compound, known as hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene, represents a fascinating area of study in organic chemistry due to its unique structure and properties. Here are several intriguing aspects:

  • Structural Intricacies: The compound features multiple fused rings and a highly condensed framework, making it an example of a polycyclic compound with extensive carbon connectivity.
  • Potential Applications: Its unique structural properties may position it as a candidate for various applications, including organic photovoltaics, materials science, and medicinal chemistry.
  • Synthetic Challenges: The synthesis of such a complex molecule often presents significant challenges in terms of selectivity, yield, and reaction conditions, making it a compelling target for synthetic chemists.
  • Research Interest: Compounds with such intricate structures are often studied for their electronic properties, as they can exhibit interesting behaviors such as luminescence and conductivity, useful in electronic applications.

As scientists continue to explore the depths of organic compounds, hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene serves as a reminder of the **endless possibilities** within the field and the **unexplored frontiers** of molecular design.


In the words of famous chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This encapsulates the spirit of exploring complex compounds, where each intriguing structure can lead to revolutionary discoveries.

Synonyms
Dibenzo[e,l]pyrene
192-51-8
Dibenzo[fg,op]naphthacene
Dibenzo[fg,op]tetracene
Dibenzo(e,l)pyrene
1,2:6,7-Dibenzpyrene
DIBENZO(FG,OP)NAPHTHACENE
1,2:6,7-Dibenzpyrene (VAN)
R1OAU0KNG7
NSC 87522
CCRIS 8722
UNII-R1OAU0KNG7
NSC-87522
Dibenzo(fg,op)naphthacene (8CI)(9CI)
DTXSID40172750
DIBENZO(E,L)PYRENE [IARC]
hexacyclo[10.10.2.02,7.08,24.013,18.019,23]tetracosa-1(23),2,4,6,8(24),9,11,13,15,17,19,21-dodecaene
Dibenzo(fg,op)tetracene
DIBENZO(E,L)PYRENE (IARC)
Dibenzo[fg,op]naphthacene; Dibenzo(e,l)pyrene; Dibenzo[fg,op]tetracene;
Dibenzo(fg,op)naphthacene (8CI)
1,7-Dibenzpyrene
NSC87522
dibenzo[fg, op]naphthacene
DTXCID6095241
CHEBI:82443
DB-220322
NS00120443
C19394
Q27155943