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 (1/1 displayed)

  • 2023Solid-state 13C NMR, X-ray diffraction and structural study of methyl 4-O-methyl β-D-glucopyranosides with all eight possible methyl-substitution patterns2citations

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Chart of shared publication
Rosenau, Thomas
1 / 13 shared
French, Alfred D.
1 / 1 shared
Potthast, Antje
1 / 16 shared
Bacher, Markus
1 / 1 shared
Hettegger, Hubert
1 / 1 shared
Roller, Alexander
1 / 16 shared
Yoneda, Yuko
1 / 1 shared
Chart of publication period
2023

Co-Authors (by relevance)

  • Rosenau, Thomas
  • French, Alfred D.
  • Potthast, Antje
  • Bacher, Markus
  • Hettegger, Hubert
  • Roller, Alexander
  • Yoneda, Yuko
OrganizationsLocationPeople

article

Solid-state 13C NMR, X-ray diffraction and structural study of methyl 4-O-methyl β-D-glucopyranosides with all eight possible methyl-substitution patterns

  • Rosenau, Thomas
  • French, Alfred D.
  • Kawada, Toshinari
  • Potthast, Antje
  • Bacher, Markus
  • Hettegger, Hubert
  • Roller, Alexander
  • Yoneda, Yuko
Abstract

<p>Cellulose model compounds that mimic the building blocks of modified cellulose and cellulose derivatives are widely used in cellulose research to infer the properties of the polymer from the monomer. Based on the well-established model compound methyl 4-O-methyl β-d-glucopyranoside, in which the methyl groups represent the truncated side chains of the cellulose, the corresponding O-methyl-substituted derivatives with all eight different substitution patterns (mono-, di- and trisubstituted at O-2, O-3, O-6) were synthesized. Crystallization of the products in sufficient quality for solid-state structure determination by single-crystal X-ray diffraction succeeded in all cases, and the results are reported. Two of the compounds showed more than one independent molecule per unit cell. Solid-state <sup>13</sup>C NMR showed a significant down-field shift (5–10 ppm) of the OMesubstituted carbons relative to the OH-substituted counterparts and generally confirmed the important influence of solid-state packing on the chemical shifts as seen by comparison to the solution NMR data.</p>

Topics
  • compound
  • polymer
  • Carbon
  • x-ray diffraction
  • cellulose
  • Nuclear Magnetic Resonance spectroscopy
  • crystallization