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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Materials Map under construction

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 (7/7 displayed)

  • 2019Dendrimers and hyper-branched polymers interacting with clays: fruitful associations for functional materials36citations
  • 2018Biomaterials Made of Phosphorus Dendrimers: Towards Diagnosis Toolscitations
  • 2016Removal of chromate from aqueous solutions by dendrimers-clay nanocomposites16citations
  • 2015Hybrid Materials Built from (Phosphorus) Dendrimerscitations
  • 2010Sensitive Sensors Based on Phosphorus Dendrimers17citations
  • 2008Organotin chemistry for the preparation of fullerene-rich nanostructures22citations
  • 2004From Calcium Interaction to Calcium Electrochemical Detection by [(C 5 H 5 )Fe(C 5 H 4 COCHCHC 6 H 4 NEt 2 )] and Its Two Novel Structurally Characterized Derivatives18citations

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Chart of shared publication
Hajjaji, Mohamed
2 / 3 shared
Caminade, Anne-Marie
4 / 28 shared
Laurent, Regis
3 / 9 shared
Beraa, Abdellah
2 / 3 shared
Caminade, A.-M.
1 / 10 shared
Majoral, Jean Pierre
2 / 33 shared
Coppel, Yannick
1 / 15 shared
Duhayon, Carine
1 / 2 shared
Gégout, Aline
1 / 1 shared
Brandli, Pierre-Elie
1 / 1 shared
Kaeser, Adrien
1 / 1 shared
Hahn, Uwe
1 / 1 shared
Nierengarten, Jean-Francois
1 / 1 shared
Sournia-Saquet, Alix
2 / 4 shared
Daran, Jean-Claude
1 / 4 shared
Maynadié, Jérôme
1 / 1 shared
Donnadieu, Bruno
1 / 4 shared
Lavabre, Dominique
1 / 1 shared
Chart of publication period
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Co-Authors (by relevance)

  • Hajjaji, Mohamed
  • Caminade, Anne-Marie
  • Laurent, Regis
  • Beraa, Abdellah
  • Caminade, A.-M.
  • Majoral, Jean Pierre
  • Coppel, Yannick
  • Duhayon, Carine
  • Gégout, Aline
  • Brandli, Pierre-Elie
  • Kaeser, Adrien
  • Hahn, Uwe
  • Nierengarten, Jean-Francois
  • Sournia-Saquet, Alix
  • Daran, Jean-Claude
  • Maynadié, Jérôme
  • Donnadieu, Bruno
  • Lavabre, Dominique
OrganizationsLocationPeople

article

Organotin chemistry for the preparation of fullerene-rich nanostructures

  • Coppel, Yannick
  • Duhayon, Carine
  • Gégout, Aline
  • Brandli, Pierre-Elie
  • Kaeser, Adrien
  • Hahn, Uwe
  • Nierengarten, Jean-Francois
  • Sournia-Saquet, Alix
  • Delavaux-Nicot, Béatrice
Abstract

Hexameric organostannoxane derivatives 3 and 4 have been prepared by treatment of 2-phenoxyacetic acid (1) and benzoic acid (2), respectively, with n-BuSn(O)OH. The drum-like structure of these compounds, made up of a prismatic Sn6O6 core, has been confirmed by 119Sn NMR spectroscopy and single-crystal X-ray diffraction analysis. The reaction conditions used for the preparation of 3 and 4 have been applied to dendritic branches with one, two or four methanofullerene subunits at the periphery and a carboxylic acid function at the focal point to produce fullerene-rich nanostructures with a stannoxane core in almost quantitative yields. These compounds have been characterized by 1H, 13C, and 119Sn NMR spectroscopy. Their electrochemical properties have been investigated by cyclic voltammetry. The central stannoxane cage has been shown not to affect the electrochemical properties of the assembled fullerenes. Indeed, each C60 moiety behaves independently, just like the parent fullerene compounds.

Topics
  • compound
  • x-ray diffraction
  • Nuclear Magnetic Resonance spectroscopy
  • cyclic voltammetry
  • carboxylic acid