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Search for "carbon nanostructures" in Full Text gives 4 result(s) in Beilstein Journal of Organic Chemistry.

Functionalization of graphene: does the organic chemistry matter?

  • Artur Kasprzak,
  • Agnieszka Zuchowska and
  • Magdalena Poplawska

Beilstein J. Org. Chem. 2018, 14, 2018–2026, doi:10.3762/bjoc.14.177

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  • therefore be excluded to ensure the efficient esterification-type reactions with graphene-family materials. Aprotic organic solvents should instead be used as a reaction medium. It is obviously a barrier for the processes with the inclusion of GO or RGO, as these carbon nanostructures’ colloidal stability
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Published 02 Aug 2018

Supramolecular frameworks based on [60]fullerene hexakisadducts

  • Andreas Kraft,
  • Johannes Stangl,
  • Ana-Maria Krause,
  • Klaus Müller-Buschbaum and
  • Florian Beuerle

Beilstein J. Org. Chem. 2017, 13, 1–9, doi:10.3762/bjoc.13.1

Graphical Abstract
  • suitable for X-ray diffraction have been obtained by slow vapor deposition of Et2O into a solution of C4 in EtOH. CCDC deposition number: 1498266. Icosahedral arrangement of functional addends for [60]fullerene hexakisadducts with dodecaacids C2 and C3 as prototypical examples for such carbon
  • nanostructures. a) Small cavities within the octahedral sites of HFF-1 filled with one CH2Cl2 molecule [57]; b) isolated cavities containing four Et2O molecules for HFF-2 (void spaces are indicated as grey surfaces and most side arms are omitted for clarity, images are created with PyMOL [58]). Face centered
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Published 02 Jan 2017

Pyrene-modified PNAs: Stacking interactions and selective excimer emission in PNA2DNA triplexes

  • Alex Manicardi,
  • Lucia Guidi,
  • Alice Ghidini and
  • Roberto Corradini

Beilstein J. Org. Chem. 2014, 10, 1495–1503, doi:10.3762/bjoc.10.154

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  • ][15][16][17][18][19][20]. Furthermore, pyrene has been shown to favour self-assembly processes of supramolecular structures [21][22][23][24][25][26][27][28] and interact with carbon nanostructures such as nanotubes [29] or graphene [30], thus allowing to create composite material with special
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Published 02 Jul 2014

Homochiral BINOL-based macrocycles with π-electron-rich, electron-withdrawing or extended spacing units as receptors for C60

  • Marco Caricato,
  • Silvia Díez González,
  • Idoia Arandia Ariño and
  • Dario Pasini

Beilstein J. Org. Chem. 2014, 10, 1308–1316, doi:10.3762/bjoc.10.132

Graphical Abstract
  • cyclic adducts exhibit recognition properties towards C60 in toluene solutions (up to log Ka = 3.2) with variable stoichiometries and variable intensities of the charge-tranfer band upon complexation. Keywords: BINOL; C60; carbon nanomaterials; carbon nanostructures; chirality; macrocycles; sensors
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Published 06 Jun 2014
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