Cyclooctadecanonaene

"Herringbone" crystal structure of [18]annulene
Names
Preferred IUPAC name (1Z,3E,5E,7Z,9E,11E,13Z,15E,17E)-Cyclooctadeca-1,3,5,7,9,11,13,15,17-nonaene
Identifiers
CAS Number	2040-73-5 N
3D model (JSmol)	Interactive image
ChemSpider	120988 N
PubChem CID	137294
InChI InChI=1S/C18H18/c1-2-4-6-8-10-12-14-16-18-17-15-13-11-9-7-5-3-1/h1-18H/b2-1-,3-1+,4-2+,5-3+,6-4+,7-5-,8-6-,9-7+,10-8+,11-9+,12-10+,13-11-,14-12-,15-13+,16-14+,17-15+,18-16+,18-17- N Key: STQWAGYDANTDNA-DWSNDWDZSA-N N InChI=1/C18H18/c1-2-4-6-8-10-12-14-16-18-17-15-13-11-9-7-5-3-1/h1-18H/b2-1-,3-1+,4-2+,5-3+,6-4+,7-5-,8-6-,9-7+,10-8+,11-9+,12-10+,13-11-,14-12-,15-13+,16-14+,17-15+,18-16+,18-17- Key: STQWAGYDANTDNA-DWSNDWDZBB
SMILES C1=CC=CC=CC=CC=CC=CC=CC=CC=C1
Properties
Chemical formula	C18H18
Molar mass	234.3 g·mol−1
Appearance	red-brown crystals
Density	1.134 g/cm3 (calc.)[1]
Structure[1]
Space group	monoclinic, P21/a
Lattice constant	a = 1.4984 (5) nm, b = 0.4802(2) nm, c = 1.0260(3) nm α = 90°, β = 111.52(1)°, γ = 90°
Formula units (Z)	2
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Cyclooctadecanonaene or [18]annulene is an organic compound with chemical formula C
₁₈H
₁₈. It belongs to the class of highly conjugated compounds known as annulenes and is aromatic. The usual isomer that [18]annulene refers to is the most stable one, containing six interior hydrogens and twelve exterior ones, with the nine formal double bonds in the cis,trans,trans,cis,trans,trans,cis,trans,trans configuration. It is reported to be a red-brown crystalline solid.

Notably, [18]annulene is the first annulene after benzene ([6]annulene) to be fully aromatic: its π-system contains 4n + 2 electrons (n = 4), and it is large enough to comfortably accommodate six hydrogen atoms in its interior, allowing it to adopt a planar shape, thus satisfying Hückel's rule. The discovery of aromatic stabilization for [18]annulene is historically significant for confirming earlier theoretical predictions based on molecular orbital theory, since simple versions of valence bond theory did not readily explain 4n + 2 rule.

The ¹H NMR of this compound exhibits hallmarks of a system with an aromatic ring current, with the 12H signal of exterior hydrogens at 9.25 ppm, while 6H signal of interior hydrogens resonates at a remarkable −2.9 ppm in THF-d₈ at −60 °C. On the other hand, a single signal at 5.45 ppm (weighted average of two individual signals) is observed at 120 °C. This is consistent with rapid exchange of exterior and interior hydrogens at that temperature. The bond lengths in [18]annulene are in between those of single and double carbon–carbon bond, with two bond lengths observed crystallographically: 138.9 pm (concave edges) and 140.7 pm (convex edges) and are indicative of significant delocalization. The favorability of delocalization is, in turn, interpreted as evidence for aromaticity. For comparison, these values are close to bond length of benzene (140 pm).^[2]

Based on enthalpy of hydrogenation, overall resonance energy has been estimated to be 37 kcal/mol.^[3] This is about the same as that of benzene; however, this energy is spread out over 18 atoms instead of 6, so [18]annulene experiences a weaker stabilization than benzene. In terms of reactivity, it is somewhat more air- and light-stable than [14]annulene and [10]annulene, which are, respectively, weakly aromatic and nonaromatic due to transannular interactions. Nevertheless, it rapidly undergoes electrophilic additions, much like other polyenes, and attempts to effect Friedel-Crafts type reactions on [18]annulene failed.^[4]

Despite the usual interpretation of [18]annulene as an 18-electron aromatic system, a 2014 theoretical study suggested that [18]annulene may be thought of as having only three completely delocalized π bonds associated with its aromaticity, while other six π bonds represent conjugated three-center-two-electron ("3c-2e") π bonds on periphery of molecule.^[5]

The compound was first synthesised by Franz Sondheimer.^[6] The original synthesis started by Eglinton reaction of di-alkyne 1,5-hexadiyne with copper(II) acetate in pyridine to give the trimer, followed by deprotonation and isomerization with potassium tert-butoxide in tert-butanol and was concluded with hydrogen organic reduction with Lindlar catalyst.^[7]

• Superbenzene