 | |
| Names | |
|---|---|
| IUPAC name Cyclonona-1,3,5,7-tetraene | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| |
| |
| Properties | |
| C9H10 | |
| Molar mass | 118.179 g·mol−1 |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Cyclononatetraene is anorganic compound with the formula C9H10. It was first prepared in 1969 by protonation of the corresponding aromatic anion (described below).[1] It is unstable and isomerizes with a half-life of 50 minutes at room temperature to 3a,7a-dihydro-1H-indene via a thermal 6π disrotatory electrocyclic ring closing.[2] Upon exposure to ultraviolet light, it undergoes a photochemical 8π electrocyclic ring closing to give bicyclo[6.1.0]nona-2,4,6-triene.[3]
Cyclononatetraenyl anion is a 10π aromatic system. Two isomers of the cyclononatetraenyl anion are known: thetrans,cis,cis,cis isomer ("Pac-Man"-shaped) and the all-cis isomer (a convexenneagon). The former is less stable and isomerizes to the latter upon warming from –40 °C to room temperature.[4]
The all-cis isomer of C9H9− can be prepared by treatment of 9-chlorobicyclo[6.1.0]nona-2,4,6-triene (1) with lithium or potassium metal.[5] Despite thering strain resulting from having C–C–C bond angles of 140° instead of the ideal 120° for sp2 carbon, this species is believed to be planar and to possessD9h symmetry. The lithium salt was found to be react with cyclopentadiene to give lithium cyclopentadienide, showing that cyclononatetraene is a weaker acid than cyclopentadiene.[6]
Cyclononatetraenyl cation is an 8π system. Its intermediacy is implicated in the solvolysis of1. The facile solvolysis of1 suggests that the cation is stabilized. Computation and experimental evidence suggest that C9H9+ is a rare example of a ground state species that exhibitsMöbius aromaticity.[7][8]
