Olympics

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Structural formula
Structural formula of Olympic
General
Surname Olympics
other names

6 H -benzo [ cd ] pyrene

Molecular formula C 19 H 12
Brief description

yellow needles

External identifiers / databases
CAS number 191-33-3
PubChem 10977566
ChemSpider 9152767
Wikidata Q62033988
properties
Molar mass 240.31 g mol −1
Physical state

firmly

Melting point

123-124 ° C

safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Olympic is a hydrocarbon . The molecule consists of five rings, four of which are benzene rings, linked together similar to the shape of the Olympic rings.

The molecule was proposed in March 2010 by Graham Richards of the University of Oxford and Antony Williams in celebration of the 2012 London Olympics . It was first synthesized by Anish Mistry and David Fox from the University of Warwick in the UK. The relative energies of olympics and its isomers were initially predicted from quantum electronic structure calculations by Andrew Valentine and David Mazziotti of the University of Chicago .

Images of the molecule were made using scanning tunneling microscopy . More detailed images were made by IBM researchers in Zurich with the help of non-contact atomic force microscopy in 2012.

See also

Individual evidence

  1. a b Morgenthaler, J .; Ruechardt, C .: New Hydrogen Transfer Catalysts . In: Eur. J. Org. Chem. 1999, 2219-2230, doi : 10.1002 / (SICI) 1099-0690 (199909) 1999: 9 <2219 :: AID-EJOC2219> 3.0.CO; 2-D .
  2. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  3. ^ AJ Williams: The Story of Olympicene from Concept to Completion . In: ChemConnector . Royal Society of Chemistry . May 27, 2012.
  4. A. Mistry: Dehydration of 3,4-dihydro-5 H -benzo [ cd ] pyrene-5-ol; 6 H -benzo [ cd ] pyrene . In: ChemSpider . Royal Society of Chemistry . May 31, 2012.
  5. ^ AJ Williams: Step by Step to the Synthesis of Olympicene . In: ChemConnector . Royal Society of Chemistry . March 14, 2012.
  6. ^ AJS Valentine, DA Mazziotti: Theoretical Prediction of the Structures and Energies of Olympicene and its Isomers . In: J. Phys. Chem. A . 117, No. 39, 2013, pp. 9746-9752. doi : 10.1021 / jp312384b .
  7. J. Palmer: 'Olympic rings' molecule olympicene in striking image . BBC News . May 28, 2012.