首页> 外文期刊>New Journal of Chemistry >Halogenation of epitaxial graphene grown on the Si-face of the SiC(0001) substrate and its further reaction with Grignard reagent
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Halogenation of epitaxial graphene grown on the Si-face of the SiC(0001) substrate and its further reaction with Grignard reagent

机译:在SiC(0001)衬底的Si面上生长的外延石墨烯的卤化及其与格氏试剂的进一步反应

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摘要

The halogenation of graphene has drawn considerable attention both from a technological and chemical point of view because fluorine- and chlorine-modified graphene can be directly used as an electronic material or as an intermediate for further modification and synthesis of composite materials. Herein, we report the reaction of fluorine, chlorine, bromine and iodine with epitaxial graphene (EG) grown on the Si-face of the SiC(0001) substrate and then the further reaction of the halogen-modified EG with Grignard reagents. Irrespective of the layer thickness, EG grown on SIC is fully fluorinated when exposed to XeF2 and reaches saturation coverage in similar to 16 h under XeF2 vapor at room temperature. Unlike fluorination, we recently reported (J. Phys. Chem. C, 2014, 118, 1014) that chlorination is very selective onto the monolayer graphene and that the chemisorbed Cl can be readily replaced by alkyl groups when treated with an alkyl Grignard reagent. In the present study, we found that not only the alkyl group, but also the chlorinated EG on SiC can be functionalized with fluoro-substituted aryl groups by reaction with an appropriate Grignard reagent. On the other hand, the fluorinated EG on SiC seems robust toward Grignard reagents. A very small concentration of bromine can be detected on EG on SiC following the reaction with Br-2 under UV tight. Iodine does not react with EG on SiC at room temperature.
机译:从技术和化学的观点来看,石墨烯的卤化已经引起了相当大的关注,因为氟和氯改性的石墨烯可以直接用作电子材料或用作进一步改性和合成复合材料的中间体。本文中,我们报道了氟,氯,溴和碘与在SiC(0001)衬底的Si面上生长的外延石墨烯(EG)的反应,然后将卤素改性的EG与格氏试剂进一步反应。不论层厚如何,当暴露于XeF2时,在SIC上生长的EG都会被完全氟化,并在室温下在XeF2蒸气下于16小时内达到饱和覆盖率。与氟化不同,我们最近报道(J. Phys。Chem。C,2014,118,1014),氯化对单层石墨烯的选择性非常高,化学吸附的Cl在用烷基格氏试剂处理时很容易被烷基取代。在本研究中,我们发现通过与适当的格氏试剂反应,不仅烷基,而且SiC上的氯化EG均可被氟取代的芳基官能化。另一方面,SiC上的氟化EG似乎对格氏试剂具有强固性。与Br-2在紫外光下反应后,在SiC上的EG上可以检测到极少量的溴。在室温下,碘不会与SiC上的EG反应。

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