Phthalonitrile
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| Names | |||
|---|---|---|---|
| Preferred IUPAC name
Benzene-1,2-dicarbonitrile[1] | |||
| Other names | |||
| Identifiers | |||
91-15-6  | |||
| 3D model (Jmol) | Interactive image | ||
| ChemSpider | 6775 | ||
| ECHA InfoCard | 100.001.859 | ||
| PubChem | 7042 | ||
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| Properties | |||
| C6H4(CN)2 | |||
| Molar mass | 128.13 g/mol | ||
| Appearance | Off-white crystals with lumps on the surface. | ||
| Odor | Almond-like | ||
| Density | 4.42[2] | ||
| Melting point | 139 to 141 °C (282 to 286 °F; 412 to 414 K) | ||
| Boiling point | sublimes | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
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| Infobox references | |||
Phthalonitrile is an organic compound with the formula C6H4(CN)2, which is an off-white crystal solid at room temperature. It is a derivative of benzene, containing two adjacent nitrile groups. The compound has low solubility in water but is soluble in common organic solvents. The compound is used as a precursor to phthalocyanine and other pigments, fluorescent brighteners, and photographic sensitizers.
Synthesis
Phthalonitrile is produced industrially in a single-stage continuous process, by the ammoxidation of o-xylene at 480 °C. The reaction is catalyzed by vanadium oxide-antimony-oxide in a fluidized bed reactor.[3]
Phthalonitrile was first described in 1896 by Johannes Pinnow. It was noted as a byproduct of the synthesis of ortho-dicyanodiazoamidobenzene via the reaction of ortho-amidobenzonitrile hydrochloride, sodium nitrite, and hydrochloric acid.[4] The first intentional synthesis involved dehydration of phthalamide by boiling in acetic anhydride.[5] Another synthesis of historical interest is the Rosenmund von Braun reaction in which an ortho substituted dihalobenzene is treated with copper(I) cyanide, which results in the halide groups being replaced by cyano groups.[6]
Applications
Phthalonitrile is the precursor to phthalocyanine pigments, a very common organic pigment.. Such pigments are generated through the reaction of phthalonitrile with various metal precursors. The reaction is carried out in a solvent at around 180 °C.[7]
Ammonolysis of phthalonitrile gives to diiminoisoindoline. This intermediate condensation with active methylene compounds to give commercially important pigment yellow 185 and pigment yellow 139.
References
- 1 2 Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 902. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
- ↑ CDC - NIOSH Pocket Guide to Chemical Hazards
- ↑ Lorz, Peter M. "Phthalic Acid and Derivatives" in Ulmanns Encyclopedia of Industrial Chemistry. Wiley-VCH: Weinheim, 2002. doi:10.1002/14356007.a20_181.pub2.
- ↑ Pinnow, Johannes; Sämann, C. "Ueber Derivate des o-Amidobenzonitrils (Derivatives of Orthamidobenzonitrile)" Berichte der Deutschen Chemischen Gesellschaft 1896, volume 29 623-32. doi:10.1002/cber.189602901118
- ↑ Braun, A.; Tscherniac, J. "Über die Produkte der Einwirkung von Acetanhydrid auf Phthalamid (Products of the Action of Acetic Anhydride on Phthalamide)" Berichte der Deutschen Chemischen Gesellschaft 1907, volume 40, pp. 2709-14. doi:10.1002/cber.190704002202
- ↑ Karl M. Kadish, Kevin M. Smith, Roger Guilard. The Porphyrin Handbook. 2003.
- ↑ Löbbert, Gerd "Phthalocyanines" in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2000. doi:10.1002/14356007.a20_213.