2-溴蒽
外观
2-溴蒽 | |
---|---|
英文名 | 2-bromoanthracene |
识别 | |
CAS号 | 7321-27-9 |
性质 | |
化学式 | C14H9Br |
摩尔质量 | 257.13 g·mol⁻¹ |
熔点 | 211—212 °C(484—485 K)[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
2-溴蒽是一种有机化合物,属溴代芳烃,化学式为C14H9Br,是溴蒽的同分异构体之一。它可由2-溴蒽酮[2]或2-溴蒽醌[3]的还原反应制备;2-蒽胺进行重氮化后再与溴化亚铜作用,也能得到2-溴蒽。[4]
参考文献
[编辑]- ^ Gianni Porzi, Carlo Concilio. Halogen—metal interconversion in 2,7-dibromonaphthalene and 2,7-dibromoanthracene. Journal of Organometallic Chemistry. 1977-03, 128 (1): 95–98 [2019-06-14]. doi:10.1016/S0022-328X(00)92039-4. (原始内容存档于2018-06-25) (英语).
- ^ Donald J. Marquardt, Frankie A. McCormick. An efficient reduction of anthrones to anthracenes. Tetrahedron Letters. 1994-02, 35 (8): 1131–1134 [2019-06-14]. doi:10.1016/0040-4039(94)88004-2. (原始内容存档于2019-08-21) (英语).
- ^ Young Ju Jang, Byung Tack Lim, Soon Byung Yoon, Ho Jun Choi, Jae Un Ha, Dae Sung Chung, Sang-Gyeong Lee. A small molecule composed of anthracene and thienothiophene devised for high-performance optoelectronic applications. Dyes and Pigments. 2015-09, 120: 30–36 [2019-06-14]. doi:10.1016/j.dyepig.2015.04.004. (原始内容存档于2018-06-19) (英语).
- ^ Einat Elmalem, Frank Biedermann, Kerr Johnson, Richard H. Friend, Wilhelm T. S. Huck. Synthesis and Photophysics of Fully π-Conjugated Heterobis-Functionalized Polymeric Molecular Wires via Suzuki Chain-Growth Polymerization. Journal of the American Chemical Society. 2012-10-24, 134 (42): 17769–17777 [2019-06-14]. ISSN 0002-7863. doi:10.1021/ja3080677. (原始内容存档于2019-04-22) (英语).