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Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
Beilstein Journal of Organic Chemistry ( IF 2.2 ) Pub Date : 2021-01-04 , DOI: 10.3762/bjoc.17.2
Daria I Tonkoglazova , Anna V Gulevskaya , Konstantin A Chistyakov , Olga I Askalepova

Novel carbazole-based [6]helicenes fused with an azine ring (pyridine, pyrazine or quinoxaline) have been prepared through a five-step synthetic sequence in good overall yields. Commercially available 2,3-dihaloazines were used as starting materials. To discern the effect of merging an azine moiety within a helical skeleton, the X-ray structures, UV–vis absorption and fluorescence spectra of the helicenes were investigated and compared to that of the parent carbazole-based [6]helicene (7H-phenanthro[3,4-c]carbazole).

中文翻译:

咔唑环与嗪环稠合的合成,晶体结构和性能

已经通过五步合成序列以良好的总收率制备了与嗪环(吡啶,吡嗪或喹喔啉)稠合的基于咔唑的新型[6]螺旋酮。使用可商购的2,3-二卤嗪作为起始原料。识别出一个螺旋形的骨架内合并吖嗪结构部分的作用下,X射线结构,UV-VIS的helicenes的吸收和荧光光谱进行了调查,相比于母体基于咔唑的[6]螺烯(7 ħ -菲[3,4- c ]咔唑)。
更新日期:2021-01-04
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