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Synthesis and characterization of nitrophenyl C_(60) derivatives

机译:硝基苯基C_(60)衍生物的合成与表征

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Studies on fullerenes have been made extensively since the method of macroscopic synthesis of fullerenes was proposed in 1990, and synthesis and structure of organic derivatives of buckminsterfullerene continue to attract interest of broad scientificcommunity. The chemical reactivity of buckminsterfullerene (C_(60)) is an area of vigorous investigation. It has been suggested that C_(60) acts like a closed-cage alkene rather than an aromatic molecule due to its poor electron-delocalization. For example, C_(60) undergoes reactions associated with the electron-deficient alkenes, Such reactions include various addition reactions, and the additions can be categorized into additions of halogens, Diels-Alder cycloaddition, nucleophilic addition, radical addition, and dipole addition. Addition of azides to C_(60) also provides an excellent method for the preparation of azafullerene derivatives. For example, by using alkyl azides, the 5, 6-azamethanoannulene was formed; by using an azidoformate derivativeand perfluorophenyl azides, the 6,6 azamethanofullerenes were produced.
机译:自从1990年提出了富勒烯的宏观合成方法以来,对富勒烯的研究已经广泛地进行了,巴克敏斯特富勒烯的有机衍生物的合成和结构一直吸引着广泛的科学界的兴趣。 buckminsterfullerene(C_(60))的化学反应性是一个有力研究的领域。已经提出,由于C_(60)的电子离域差,其行为像闭笼烯烃而不是芳族分子。例如,C_(60)经历与缺电子的烯烃相关的反应。这样的反应包括各种加成反应,并且该加成可分为卤素的加成,Diels-Alder环加成,亲核加成,自由基加成和偶极加成。将叠氮化物添加到C_(60)中也为制备氮杂富勒烯衍生物提供了一种极好的方法。例如,通过使用烷基叠氮化物,形成了5,6-氮杂亚甲基环戊烯;通过使用叠氮基甲酸酯衍生物和全氟苯基叠氮化物,制备了6,6-氮杂甲基富勒烯。

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