Eisspeedway

Hexa-cata-hexabenzocoronene

Hexa-cata-hexabenzocoronene
Names
Preferred IUPAC name
Trinaphtho[1,2,3,4-fgh:1′,2′,3′,4′-pqr:1′′,2′′,3′′,4′′-za1b1]trinaphthylene
Other names
Hexabenzo[a,d,g,j,m,p]coronene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.012.641 Edit this at Wikidata
UNII
  • InChI=1S/C48H24/c1-2-14-26-25(13-1)37-27-15-3-4-16-28(27)39-31-19-7-8-20-32(31)41-34-22-10-12-24-36(34)42-35-23-11-9-21-33(35)40-30-18-6-5-17-29(30)38(26)44-43(37)45(39)47(41)48(42)46(40)44/h1-24H
    Key: XHJPOZDMDBETDO-UHFFFAOYSA-N
  • C1=CC=C2C(=C1)C3=C4C5=C2C6=CC=CC=C6C7=C5C8=C(C9=CC=CC=C97)C1=CC=CC=C1C1=C8C4=C(C2=CC=CC=C23)C2=CC=CC=C21
Properties
C48H24
Molar mass 600.720 g·mol−1
Appearance Yellow–orange solid[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hexa-cata-hexabenzocoronene (hexabenzo[a,d,g,j,m,p]coronene) is a polycyclic aromatic hydrocarbon with the molecular formula C48H24. It consists of a central coronene molecule, with an additional benzene ring fused onto each ring around the periphery.

Hexa-cata-hexabenzocoronene has a contorted structure due to steric crowding among the benzene rings around the edge,[2] analogous to the situation in benzo[c]phenanthrene.

See also

References

  1. ^ Xiao, Shengxiong; Myers, Matthew; Miao, Qian; Sanaur, Sébastien; Pang, Keliang; Steigerwald, Michael L.; Nuckolls, Colin (2005). "Molecular Wires from Contorted Aromatic Compounds". Angew. Chem. Int. Ed. Engl. 44 (45): 7390–7394. doi:10.1002/anie.200502142. PMID 16173105.
  2. ^ Chiu, Chien-Yang; Kim, Bumjung; Gorodetsky, Alon A.; Sattler, Wesley; Wei, Sujun; Sattler, Aaron; Steigerwald, Michael; Nuckolls, Colin (2011). "Shape-shifting in contorted dibenzotetrathienocoronenes". Chem. Sci. 2: 1480–1486. doi:10.1039/C1SC00156F.