Lophine is the organic compound with the formula (C6H5C)2N2HCC6H5. It is a derivative of imidazole wherein all three carbon atoms have phenyl groups as substituents. A white solid, this compound gave the first example of chemiluminescence when its basic solutions were exposed to air.[1] Its chemiluminescence continues to attract attention.[2]
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| Names | |
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| Other names
2,4,5-triphenylimidazole
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| Identifiers | |
| ECHA InfoCard | 100.006.915 |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C21H16N2 | |
| Molar mass | 296.373 g·mol−1 |
| Appearance | white solid |
| Density | 1,0874 g/cm3 |
| Melting point | 275 °C (527 °F; 548 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Lophine and its dihydro analogue amarine (meso-2,4,5-triphenyl-2-imidazoline[3]) were discovered early in the history of organic chemistry (between 1841 and 1847),[4] before the development of a structural theory of organic chemistry by Kekulé and Couper in the 1850s. Lophine is prepared by condensation of benzaldehyde, benzil, and ammonia.[5]
References
edit- ^ Radziszewski, B. R. (1877). "Untersuchungen über Hydrobenzamid, Amarin und Lophin". Berichte der Deutschen Chemischen Gesellschaft. 10: 70–75. doi:10.1002/cber.18770100122.
- ^ Nakashima, Kenichiro (2003). "Lophine derivatives as versatile analytical tools". Biomedical Chromatography. 17 (2–3): 83–95. doi:10.1002/bmc.226. PMID 12717796.
- ^ Huang, Xue-Feng; Song, Yu-Mei; Wang, Xi-Sen; Pang, Jie; Zuo, Jing-Lin; Xiong, Ren-Gen (2006-02-15). "Crystal structures of amarine and isoamarine and copper(I) coordination chemistry with their allylation products". Journal of Organometallic Chemistry. 691 (5): 1065–1074. doi:10.1016/j.jorganchem.2005.10.040. ISSN 0022-328X.
- ^ Japp, Francis R.; Robinson, H. H. (1882-01-01). "L.—On the constitution of amarine and lophine". Journal of the Chemical Society, Transactions. 41 (0): 323–329. doi:10.1039/CT8824100323. ISSN 0368-1645.
- ^ Bandivadekar, Priyanka V.; Chaturbhuj, Ganesh U. (2024). "Catalyst-free one-pot synthesis of 2,4,5-tri- and 1,2,4,5-tetrasubstituted imidazoles". Journal of Heterocyclic Chemistry. 61 (3): 430–438. doi:10.1002/jhet.4771.