| Azulene | |
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bicyclo[5.3.0]decapentaene |
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| Identifiers | |
| CAS number | 275-51-4 |
| PubChem | 9231 |
| ChemSpider | 8876 |
| UNII | 82R6M9MGLP |
| KEGG | C13392 |
| ChEBI | CHEBI:31249 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C10H8 |
| Molar mass | 128.17 g mol−1 |
| Melting point |
99–100 °C |
| Boiling point |
242 °C |
| Solubility in water | 0.02 g/l[1] |
| Thermochemistry | |
| Std enthalpy of combustion ΔcH |
-1266.5 kcal/mol[2] |
| (verify) (what is: /?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Azulene is an organic compound and an isomer of naphthalene. Whereas naphthalene is colourless, azulene is dark blue. Its name is derived from the Spanish word azul, meaning "blue". Two terpenoids, vetivazulene (4,8-dimethyl-2-isopropylazulene) and guaiazulene (1,4-dimethyl-7-isopropylazulene), that feature the azulene skeleton are found in nature as constituents of pigments in mushrooms, guaiac wood oil, and some marine invertebrates.
Azulene has a long history, dating back to the 15th century as the azure-blue chromophore obtained by steam distillation of German chamomile. The chromophore was discovered in yarrow and wormwood and named in 1863 by Septimus Piesse. Its structure was first reported by Lavoslav Ružička, followed by its organic synthesis in 1937 by Placidus Plattner.
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Azulene is usually viewed as resulting from fusion of cyclopentadiene and cycloheptatriene rings. Like naphthalene and cyclodecapentaene, it is a 10 pi electron system. It exhibits aromatic properties: (i) the peripheral bonds have similar lengths and (ii) it undergoes Friedel-Crafts-like substitutions. The stability gain from aromaticity is estimated to be half that of naphthalene.
Its dipole moment is 1.08 D,[4] in contrast with naphthalene, which has a dipole moment of zero. This polarity can be explained by regarding azulene as the fusion of the aromatic 6 π-electron cyclopentadienyl anion and aromatic 6 π-electron tropylium cation. In order to achieve the stable aromatic sextet in both rings, one electron from the seven-membered ring is transferred to the five-membered ring. Reactivity studies confirm that seven-membered ring is electrophilic and the five-membered ring is nucleophilic. The dipolar nature of the ground state is reflected in its deep colour, which is unusual for small unsaturated aromatic compounds. Another notable feature of azulene is that it violates Kasha's rule by exhibiting fluorescence from an upper-excited state (S2 → S0).[5]
Synthetic routes to azulene have long been of interest because of its unusual structure. In 1939 the first method was reported by St. Pfau and Plattner [6] starting from indane and ethyl diazoacetate.
An efficient one-pot route entails annulation of cyclopentadiene with unsaturated C5-synthons.[7] The alternative approach from cycloheptatriene has long been known, one illustrative method being shown below.[8]
In organometallic chemistry, azulene serves as a ligand for low-valent metal centers, which otherwise are known to form π-complexes with both cyclopentadienyl and cycloheptatrienyl ligands. Illustrative complexes are (azulene)Mo2(CO)6 and (azulene)Fe2(CO)5.[9]
In naphth[a]azulenes, a naphthalene ring is condensed at the 1,2-positions of azulene. In one such system[10] deformation from planarity is found similar to that of tetrahelicene.
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