Azulene is an organic compound and an isomer of naphthalene. Whereas naphthalene is colourless, azulene is dark 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.
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|Systematic IUPAC name
3D model (JSmol)
|Molar mass||g·mol−1 128.174|
|Melting point||99 to 100 °C (210 to 212 °F; 372 to 373 K)|
|Boiling point||242 °C (468 °F; 515 K)|
Std enthalpy of
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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.
Structure and bondingEdit
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, in contrast with naphthalene, which has a dipole moment of zero. This polarity can be explained by regarding azulene as the fusion of a 6 π-electron cyclopentadienyl anion and a 6 π-electron tropylium cation: one electron from the seven-membered ring is transferred to the five-membered ring to give each ring aromatic stability by Hückel's rule. 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).
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  starting from indane and ethyl diazoacetate.
An efficient one-pot route entails annulation of cyclopentadiene with unsaturated C5-synthons. The alternative approach from cycloheptatriene has long been known, one illustrative method being shown below.
Procedure: step 1: cycloheptatriene 2+2 cycloaddition with dichloro ketene step 2: diazomethane insertion reaction step 3: dehydrohalogenation reaction with DMF step 4: Luche reduction to alcohol with sodium borohydride step 5: elimination reaction with Burgess reagent step 6: oxidation with p-chloranil step 7: dehalogenation with polymethylhydrosiloxane, palladium(II) acetate, potassium phosphate and the DPDB ligand
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.
1-Hydroxyazulene is an unstable green oil and it does not show keto–enol tautomerism. 2-Hydroxyazulene is obtained by hydrolysis of 2-methoxyazulene with hydrobromic acid. It is stable and does show keto–enol tautomerism. The pKa of 2-hydroxyazulene in water is 8.71. It is more acidic than phenol or naphthol. The pKa of 6-hydroxyazulenes in water is 7.38 making it also more acidic than phenol or naphthol.
Guaiazulene (1,4-dimethyl-7-isopropylazulene) is an alkylated derivative of azulene with an almost identical intensely blue colour. It is commercially available to the cosmetics industry where it functions as a skin conditioning agent.
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