Synthesis of Multifluoromethylated γ-Sultines by a Photoinduced Radical Addition–Polar Cyclization

Despite the significance of sultines in synthesis, medicine, and materials science, the chemistry of sultines has remained unexplored due to their inaccessibility. Herein, we demonstrate the development of a photoredox-catalyzed multifluoromethyl radical addition/SO₂ incorporation/polar cyclization cascade approach to multifluoromethylated γ-sultines. The reactions proceed by single electron transfer induced multifluoromethyl radical addition to an alkene followed by SO₂ incorporation, and single-electron reduction for polar 5-exo-tet cyclization. Key to the success of the protocol is the use of easily oxidizable multifluoroalkanesulfinates as bifunctional reagents. The reactions proceed with excellent functional-group tolerance to deliver γ-sultines in moderate to excellent yields.     

Effect of electrode charge balance on the energy storage performance of hybrid supercapacitor cells based on LiFePO4 as Li-ion battery electrode and activated carbon

Journal of Solid State Electrochemistry - Hybrid supercapacitors using asymmetric, LiFePO4 (LFP) lithium intercalation and electric double layer activated carbon (AC) electrodes combining the high...     

丹皮酚噻唑类化合物的合成及其细胞毒性评价

本文以丹皮酚为原料合成了15个新型丹皮酚噻唑衍生物,利用IR、~1H NMR、~(13)C NMR和MS对所得化合物的结构进行表征,采用MTT法考察了目标化合物对MGC-803(胃癌细胞)、LOVO(结肠癌细胞)、T-24(膀胱癌细胞) 3种细胞的体外抗肿瘤活性。结果表明,部分化合物具有良好的细胞毒活性,其中化合物4b、4e、4f、4h、4l对MGC-803的细胞毒性优于阳性对照药顺铂,尤其是化合物4b对MGC-803、LOVO和T-24三种肿瘤细胞的IC_(50)值分别为11. 39±4. 46、2. 06±1. 27和6. 03±0. 86μg/m L,值得进一步研究。     

α-异丙基对卤苯乙酸拆分方法的改进

α-甲基苄胺;α-异丙基对卤苯乙酸拆分方法的改进     

Self-Catalyzed Hydroxyl-Yne Click Reaction: A Powerful Tool toward Red-Emitting Nontraditional Small Organic Luminogens

Nontraditional small organic luminogens (NTSOLs) without classic conjugated chromophores have attracted significant attention. However, the design and synthesis of NTSOLs with fluorescence in the red region remain significantly challenging. In this study, we established a self-catalyzed hydroxyl-yne click reaction for preparing long-wavelength and red-emitting NTSOLs. Owing to their perfect reaction selectivity, high efficiency, and excellent universality, a series of compounds with well-defined structures were obtained in high yields. Moreover, the obtained compounds showed concentration-enhanced and excitation-dependent emission characteristics. The compounds also exhibited dramatical chemical structure-dependent and aggregation-induced red-shifted fluorescence properties, based on which we successfully obtained red-emitting NTSOLs by simply adjusting chemical structure and concentration. Also, the compounds show good cell staining ability, which can be used in cell imaging.