首页> 外文OA文献 >Purely Armchair or Partially Chiral: Noncontact Atomic Force Microscopy Characterization of Dibromo-Bianthryl-Based Graphene Nanoribbons Grown on Cu(111)
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Purely Armchair or Partially Chiral: Noncontact Atomic Force Microscopy Characterization of Dibromo-Bianthryl-Based Graphene Nanoribbons Grown on Cu(111)

机译:纯粹的扶手椅或部分手性:非接触的原子力显微镜显微镜表征在Cu(111)上生长的基于二溴二割的石墨烯纳米波巴

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摘要

We report on the atomic structure of graphene nanoribbons (GNRs) formed via on-surface synthesis from 10,10′-dibromo-9,9′-bianthryl (DBBA) precursors on Cu(111). By means of ultrahigh vacuum noncontact atomic force microscopy with CO-functionalized tips we unveil the chiral nature of the so-formed GNRs, a structure that has been under considerable debate. Furthermore, we prove that—in this particular case—the coupling selectivity usually introduced by halogen substitution is overruled by the structural and catalytic properties of the substrate. Specifically, we show that identical chiral GNRs are obtained from 9,9′-bianthryl, the unsubstituted sister molecule of DBBA.
机译:我们报告通过在Cu(111)上的10,10'-dibromo-9,9'-二硫酸酯(DBBA)前体的表面合成形成的石墨烯纳米纤维(GNRS)的原子结构。通过超高压真空非接触原子力显微镜,具有共同官能化提示,我们揭示了所形成的GNR的手性性,这是一项具有相当大辩论的结构。此外,我们证明,在这种特殊情况下,通常通过卤素取代引入的偶联选择性通过基材的结构和催化性质来克服。具体而言,我们表明,相同的手性GNR是从9,9'-Bianthryl,DBBA未取代的姐妹分子获得的。

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