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Selective Dispersion of Single-Walled Carbon Nanotubes with Specific Chiral Indices by Poly(N-decyl-2,7-carbazole)

机译:聚(N-癸基-2,7-咔唑)具有特定手性指标的单壁碳纳米管的选择性分散

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摘要

Physico-chemical methods to sort single-walled carbon nanotubes (SWNTs) by chiral index are presently lacking but are required for in-depth experimental analysis and also for potential future applications of specific species. Here we report the unexpected selectivity of poly-(N-decyl-2,7-carbazole) to almost exclusively disperse semiconducting SWNTs with differences of their chiral indices (n - m) ≥ 2 in toluene. The observed selectivity complements perfectly the dispersing features of the fluorene analogue poly(9,9-dialkyl-2,7-fluorene), which disperses semiconducting SWNTs with (h - m) ≤ 2 in toluene. The dispersed samples are fuerther purified by density gradient centrifugation and analyzed by photoluminescence excitation spectroscopy. All-atom molecular modeling with decamer model compounds of the polymers and (10,2) and (7,6) SWNTs suggests differences in the π-π stacking interaction as origin of the selectivity. We observe energetically favored complexes between the (10,2) SWNT and the carbazole decamer and between the (7,6) SWNT and the fluorene decamer, respectively. These findings demonstrate that subtle structural changes of polymers lead to selective solvation of different families of carbon nanotubes. fuerthermore, chemical screening of closely related polymers may pave the way toward simple, low-cost, and index-specific isolation of SWNTs.
机译:目前尚缺乏通过手性指数对单壁碳纳米管(SWNT)进行分类的物理化学方法,但对于深入的实验分析以及特定物种的潜在未来应用而言,这是必需的。在这里,我们报道了聚(N-癸基-2,7-咔唑)对几乎全部分散的半导体手性碳纳米管具有出乎意料的选择性,它们的手性指数(n-m)≥2在甲苯中的差异。观察到的选择性完美地补充了芴类似物聚(9,9-二烷基-2,7-芴)的分散特性,后者将(h-m)≤2的半导体SWNT分散在甲苯中。分散的样品通过密度梯度离心进一步纯化,并通过光致发光激发光谱法进行分析。用聚合物和(10,2)和(7,6)SWNT的decamer模型化合物进行的全原子分子建模表明,π-π堆积相互作用的差异是选择性的起源。我们分别观察到(10,2)SWNT和咔唑十聚体之间以及(7,6)SWNT和芴十聚体之间在能量上有利的配合物。这些发现表明,聚合物的细微结构变化导致不同家族的碳纳米管的选择性溶剂化。此外,化学筛选紧密相关的聚合物可能为SWNT的简单,低成本和特定于指数的分离铺平道路。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第4期|p.652-655|共4页
  • 作者单位

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany;

    Institut fuer Technische Chemie und Polymerchemie, Karlsruher Institut fuer Technologie, 76128 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany;

    Institut fuer Technische Chemie und Polymerchemie, Karlsruher Institut fuer Technologie, 76128 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany,DFG Center for Functional Nanostructures, 76028 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany,DFG Center for Functional Nanostructures, 76028 Karlsruhe, Germany,Institut fuer Physikalische Chemie, Karlsruher Institut fuer Technologie, 76128 Karlsruhe, Germany;

    Institut fuer Nanotechnologie, Karlsruher Institut fuer Technologie, 76021 Karlsruhe, Germany,DFG Center for Functional Nanostructures, 76028 Karlsruhe, Germany,Department of Chemistry, University of Basel, 4056 Basel, Switzerland;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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