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Search for "nanocarbon" in Full Text gives 5 result(s) in Beilstein Journal of Organic Chemistry.

Spin and charge interactions between nanographene host and ferrocene

  • Akira Suzuki,
  • Yuya Miyake,
  • Ryoga Shibata and
  • Kazuyuki Takai

Beilstein J. Org. Chem. 2024, 20, 1011–1019, doi:10.3762/bjoc.20.89

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  • interactions between the nanographene host and the guest molecules will be a promising strategy for developing a new class of molecular magnets. Keywords: charge transfer; ferrocene; graphene; host–guest; spin interaction; Introduction Nanocarbon host material, which is based on elements free from resource
  • mesoporous silica (MCM-41) [18]. So, ferrocene is expected to exhibit strong host–guest interactions with a nanographene host through π–π stacking. Regarding ferrocene as a guest molecule for nanocarbon hosts, carbon nanotubes (CNTs) have been used to accommodate guest ferrocene molecules, where the amount
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Letter
Published 02 May 2024

Facile access to pyridinium-based bent aromatic amphiphiles: nonionic surface modification of nanocarbons in water

  • Lorenzo Catti,
  • Shinji Aoyama and
  • Michito Yoshizawa

Beilstein J. Org. Chem. 2024, 20, 32–40, doi:10.3762/bjoc.20.5

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  • , and graphene nanoplatelets) are achieved through noncovalent encircling with the bent amphiphiles. The resultant imidazole-modified nanocarbons display a pH-responsive surface charge, as evidenced by NMR and zeta-potential measurements. In addition, solubilization of a nitrogen-doped nanocarbon (i.e
  • ., graphitic carbon nitride) in the form of 10–30 nm-sized stacks is also demonstrated using the present amphiphiles. Keywords: aromatic micelle; nanocarbon; nonionic surface modification; pyridinium; water-solubilization; Introduction Nanocarbons, such as fullerenes, graphenes, and carbon nanotubes, are
  • ][9][10][11]. The development of new amphiphiles with large polyaromatic panels for strong aromatic–aromatic interactions and nonionic side-chains on the other hand would grant access to water-soluble nanocarbons with tunable surface properties, which could expand noncovalent nanocarbon chemistry and
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Full Research Paper
Published 08 Jan 2024

Six-fold C–H borylation of hexa-peri-hexabenzocoronene

  • Mai Nagase,
  • Kenta Kato,
  • Akiko Yagi,
  • Yasutomo Segawa and
  • Kenichiro Itami

Beilstein J. Org. Chem. 2020, 16, 391–397, doi:10.3762/bjoc.16.37

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  • Mai Nagase Kenta Kato Akiko Yagi Yasutomo Segawa Kenichiro Itami Graduate School of Science, Nagoya University, Chikusa, Nagoya, 464-8602, Japan JST-ERATO, Itami Molecular Nanocarbon Project, Nagoya, 464-8602, Japan Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa
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Published 13 Mar 2020

Mechanochemistry-assisted synthesis of hierarchical porous carbons applied as supercapacitors

  • Desirée Leistenschneider,
  • Nicolas Jäckel,
  • Felix Hippauf,
  • Volker Presser and
  • Lars Borchardt

Beilstein J. Org. Chem. 2017, 13, 1332–1341, doi:10.3762/bjoc.13.130

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  • ]. For example, the preparation of nanocarbon structures such as graphene sheets or fullerenes [39][40][41] as well as porous carbonaceous polymers [42][43] have been conducted mechanochemically. Our work demonstrates that a templating approach can be transferred into the solvent-free environment of a
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Published 06 Jul 2017

Pyridylidene ligand facilitates gold-catalyzed oxidative C–H arylation of heterocycles

  • Kazuhiro Hata,
  • Hideto Ito,
  • Yasutomo Segawa and
  • Kenichiro Itami

Beilstein J. Org. Chem. 2015, 11, 2737–2746, doi:10.3762/bjoc.11.295

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  • Kazuhiro Hata Hideto Ito Yasutomo Segawa Kenichiro Itami Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan JST, ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya
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Published 28 Dec 2015
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