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首页> 外文期刊>Acta Chimica Slovenica >Strueture of 7,9,12,15,18,20,39,24,45,57-C_(60)(CF3)_(10)(1,2:3,4-O)2. The First Regiospecific Diepoxidation of a Fullerene Derivative
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Strueture of 7,9,12,15,18,20,39,24,45,57-C_(60)(CF3)_(10)(1,2:3,4-O)2. The First Regiospecific Diepoxidation of a Fullerene Derivative

机译:结构7,9,12,15,18,20,39,24,45,57-C_(60)(CF 3)_(10)(1,2:3,4-O)2。 富勒烯衍生物的第一种再生环氧化

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摘要

An unusual regiospecific diepoxidation of an isomer of C_(60)(CF3)_(10) was discovered to slowly occur in solution while exposed to air. This is the only known example of a perfluoroalkyl fullerene undergoing epoxidation under ambient conditions. This compound was characterized by a variety of analytical methods including ~(19)F NMR spectroscopy, APCI-MS, UV-vis spectroscopy, and X-ray crystallography. Numerous oxidation methods were explored including ozonation, photolysis, thermolysis, and the chemical oxidation by m-chloroperoxobenzoic acid, none of which has yielded the diepoxide. This indicated that the process is kinetically very slow, presumably due to steric crowding around the oxygen addition sites. These findings of spontaneous diepoxidation of the otherwise stable compound have far reaching implications as more fullerenes and fullerene derivatives are being used in organic electronics, and their instability toward oxidation in ambient conditions may alter the performance of the device.
机译:发现C_(60)(CF3)(CF3)(10)的异构体的异常细胞染色,在暴露于空气中慢慢发生在溶液中。这是在环境条件下经历环氧化的全氟烷基富勒烯的唯一已知的例子。该化合物的特征在于各种分析方法,包括〜(19)F NMR光谱,APCI-MS,UV-Vis光谱和X射线晶体学。探索了许多氧化方法,包括臭氧化,光解,热解和M-氯氧己基苯甲酸的化学氧化,其中没有分析掺杂剂。这表明该过程是动力学上非常缓慢的,可能是由于氧气添加位点周围的空间拥挤。这些稳定的化合物的自发点化的这些发现具有远远达到有机电子产品和富勒烯和富勒烯衍生物的影响,并且它们对环境条件下的氧化的不稳定性可能会改变装置的性能。

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