摘要
The acylation of 5-aryl dipyrromethanes afforded products with interestingly rich substitution modes, i.e., alpha- and beta-monoacylated (modes a and b), and &ALPHA, &ALPHA'-, &ALPHA, &BETA'- and &BETA, &BETA'-diacylated (modes c-e). Especially, the &BETA- and &BETA, &BETA'-acylation modes are unprecedented. And most of these products can be synthesized at a gram scale. The anisoyl substituted 5-(4-cyanophenyl) dipyrromethanes (1a-1e) were oxidized with DDQ. Thus, 1a and 1b afforded the corresponding dipyrrins 1a-DPR, and 1b-DPR. More interestingly, the diacylated ones 1c-1e could not be oxidized by DDQ. Instead, 1c-OH-1e-OH were obtained with a hydroxyl group attached to the 5-position. 1a-DPR-1e-OH were further developed as fluorescence turn-on Zn2+ probes. 1d-OH showed the highest sensitivity, with a detection limit of 1.5 x 10(-8) M, and it was successfully applied in Zn2+ imaging in Hela cells. Furthermore, single crystals of two Zn2+ complexes were obtained and analyzed by X-ray diffraction.
- 出版日期2015-1
- 单位华东理工大学