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β-Fluorinated porpholactones and metal complexes: synthesis, characterization and some spectroscopic studies
Inorganic Chemistry Frontiers ( IF 6.1 ) Pub Date : 2017-07-24 00:00:00 , DOI: 10.1039/c7qi00375g
Ji-Yun Hu 1, 2, 3, 4, 5 , Zhuo-Yan Wu 1, 2, 3, 4, 5 , Ke Chai 5, 6, 7, 8 , Zi-Shu Yang 1, 2, 3, 4, 5 , Yin-Shan Meng 1, 2, 3, 4, 5 , Yingying Ning 1, 2, 3, 4, 5 , Jing Zhang 5, 6, 7, 8 , Jun-Long Zhang 1, 2, 3, 4, 5
Affiliation  

We describe the synthesis of β-fluorinated porpholactones by oxidation of the fluorinated C[double bond, length as m-dash]C bond of the pyrrolic subunit in porphyrin using the “RuCl3 + Oxone®” protocol. The electron-withdrawing effects of β-fluorine on the absorption, fluorescence, phosphorescence and redox properties of the β-fluoroporpholactones were studied. A potential application of the β-fluoroporpholactones was demonstrated in sensitizing near-IR (NIR) emissive ytterbium, giving a high quantum yield (58%) and long luminescence time (525 μs) in CD2Cl2.

中文翻译:

β-氟代内酯和金属配合物:合成,表征和一些光谱学研究

我们描述了[双键,长度为m-破折号]使用“ RuCl 3 +Oxone®”方案,通过氧化卟啉中吡咯亚基的氟化C C键来合成β-氟化卟啉内酯。研究了β-氟对β-氟卟啉内酯的吸收,荧光,磷光和氧化还原性质的吸电子作用。证明了β-氟代内酯在将近红外(NIR)发光致敏方面的潜在应用,可在CD 2 Cl 2中提供高量子产率(58%)和长发光时间(525μs)。
更新日期:2017-09-12
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