Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2023Curved graphene nanoribbons derived from tetrahydropyrene-based polyphenylenes via one-pot K-region oxidation and Scholl cyclization6citations
  • 2021Coordination of trivalent lanthanum and cerium, and tetravalent cerium and actinides (An = Th(iv), U(iv), Np(iv)) by a 4-phosphoryl 1H-pyrazol-5-olate ligand in solution and the solid state18citations
  • 2020Innentitelbild: P‒P Condensation and P‒N/P‒P Bond Metathesis: Facile Synthesis of Cationic Tri‑ and Tetraphosphanes (Angew. Chem. 9/2020)citations

Places of action

Chart of shared publication
Hansen, Michael Ryan
1 / 12 shared
Weigand, Jan J.
3 / 6 shared
Guerrero-León, L. Andrés
1 / 1 shared
Arisnabarreta, Nicolás
1 / 1 shared
Böckmann, Steffen
1 / 1 shared
Melidonie, Jason
1 / 2 shared
Zheng, Wenhao
1 / 1 shared
Obermann, Sebastian
1 / 1 shared
Feng, Xinliang
1 / 58 shared
Feyter, Steven De
1 / 13 shared
Beljonne, David
1 / 44 shared
Wang, Hai I.
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Ma, Ji
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Osella, Silvio
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Bonn, Mischa
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Schnaars, Kathleen
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Schwedtmann, Kai
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Zhang, Jianfeng
1 / 1 shared
Kraus, Florian
1 / 18 shared
März, Juliane
1 / 1 shared
Stumpf, Thorsten
1 / 4 shared
Rossberg, André
1 / 3 shared
Kaden, Peter
1 / 2 shared
Wolf, Robert
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Somsook, Ekasith
1 / 2 shared
Taube, Clemens
1 / 1 shared
Noikham, Medena
1 / 1 shared
Chart of publication period
2023
2021
2020

Co-Authors (by relevance)

  • Hansen, Michael Ryan
  • Weigand, Jan J.
  • Guerrero-León, L. Andrés
  • Arisnabarreta, Nicolás
  • Böckmann, Steffen
  • Melidonie, Jason
  • Zheng, Wenhao
  • Obermann, Sebastian
  • Feng, Xinliang
  • Feyter, Steven De
  • Beljonne, David
  • Wang, Hai I.
  • Ma, Ji
  • Osella, Silvio
  • Bonn, Mischa
  • Schnaars, Kathleen
  • Wenzel, Marco
  • Schwedtmann, Kai
  • Zhang, Jianfeng
  • Kraus, Florian
  • März, Juliane
  • Stumpf, Thorsten
  • Rossberg, André
  • Kaden, Peter
  • Wolf, Robert
  • Somsook, Ekasith
  • Taube, Clemens
  • Noikham, Medena
OrganizationsLocationPeople

article

Curved graphene nanoribbons derived from tetrahydropyrene-based polyphenylenes via one-pot K-region oxidation and Scholl cyclization

  • Hansen, Michael Ryan
  • Hennersdorf, Felix
  • Weigand, Jan J.
  • Guerrero-León, L. Andrés
  • Arisnabarreta, Nicolás
  • Böckmann, Steffen
  • Melidonie, Jason
  • Zheng, Wenhao
  • Obermann, Sebastian
  • Feng, Xinliang
  • Feyter, Steven De
  • Beljonne, David
  • Wang, Hai I.
  • Ma, Ji
  • Osella, Silvio
  • Bonn, Mischa
Abstract

<p>Precise synthesis of graphene nanoribbons (GNRs) is of great interest to chemists and materials scientists because of their unique opto-electronic properties and potential applications in carbon-based nanoelectronics and spintronics. In addition to the tunable edge structure and width, introducing curvature in GNRs is a powerful structural feature for their chemi-physical property modification. Here, we report an efficient solution synthesis of the first pyrene-based GNR (PyGNR) with curved geometry via one-pot K-region oxidation and Scholl cyclization of its corresponding well-soluble tetrahydropyrene-based polyphenylene precursor. The efficient A<sub>2</sub>B<sub>2</sub>-type Suzuki polymerization and subsequent Scholl reaction furnishes up to ∼35 nm long curved GNRs bearing cove- and armchair-edges. The construction of model compound 1, as a cutout of PyGNR, from a tetrahydropyrene-based oligophenylene precursor proves the concept and efficiency of the one-pot K-region oxidation and Scholl cyclization, which is clearly revealed by single crystal X-ray diffraction analysis. The structure and optical properties of PyGNR are investigated by Raman, FT-IR, solid-state NMR, STM and UV-Vis analysis with the support of DFT calculations. PyGNR exhibits a narrow optical bandgap of ∼1.4 eV derived from a Tauc plot, qualifying as a low-bandgap GNR. Moreover, THz spectroscopy on PyGNR estimates its macroscopic charge mobility μ as ∼3.6 cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup>, outperforming several other curved GNRs reported via conventional Scholl reaction.</p>

Topics
  • impedance spectroscopy
  • compound
  • single crystal X-ray diffraction
  • single crystal
  • Carbon
  • mobility
  • density functional theory
  • Nuclear Magnetic Resonance spectroscopy
  • scanning tunneling microscopy