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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1.080 Topics available

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977 Locations available

693.932 PEOPLE
693.932 People People

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Lancaster University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2022Efficient solid-state photoswitching of methoxyazobenzene in a metal–organic framework for thermal energy storage18citations
  • 2022A structural investigation of organic battery anode materials by NMR crystallography7citations
  • 2021Solid-state nuclear magnetic resonance study of polymorphism in tris(8-hydroxyquinolinate)aluminium2citations
  • 2021Effect of Transition Metal Substitution on the Flexibility and Thermal Properties of MOF-Based Solid-Solid Phase Change Materials10citations
  • 2020Long-Term Solar Energy Storage under Ambient Conditions in a MOF-Based Solid–Solid Phase-Change Material44citations
  • 2016Towards Robust Electroactive Biomaterialscitations
  • 2014Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities8citations

Places of action

Chart of shared publication
Griffiths, Kieran
4 / 5 shared
Griffin, John
2 / 4 shared
Desai, Aamod V.
1 / 1 shared
Seymour, Valerie Ruth
1 / 2 shared
Griffin, John M.
1 / 7 shared
Morris, Russell E.
1 / 30 shared
Whewell, Tommy
1 / 1 shared
Armstrong, A. Robert
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Griffin, J. M.
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Cervini, L.
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Cross, C.
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Shah, Sayed
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Hardy, John George
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Mort, Richard
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Robinson, Bj
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Firlak, Melike
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Geier, Michael J.
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Westcott, Stephen A.
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Lee, Graham M.
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Decken, Andreas
1 / 6 shared
Oneill, Taryn
1 / 1 shared
Webb, Michael I.
1 / 1 shared
Vogels, Christopher M.
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Bowes, Eric G.
1 / 1 shared
Flewelling, Andrew
1 / 1 shared
Gray, Christopher A.
1 / 1 shared
Li, Haoxin
1 / 1 shared
Chart of publication period
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2021
2020
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2014

Co-Authors (by relevance)

  • Griffiths, Kieran
  • Griffin, John
  • Desai, Aamod V.
  • Seymour, Valerie Ruth
  • Griffin, John M.
  • Morris, Russell E.
  • Whewell, Tommy
  • Armstrong, A. Robert
  • Griffin, J. M.
  • Cervini, L.
  • Cross, C.
  • Shah, Sayed
  • Hardy, John George
  • Mort, Richard
  • Robinson, Bj
  • Firlak, Melike
  • Geier, Michael J.
  • Westcott, Stephen A.
  • Lee, Graham M.
  • Decken, Andreas
  • Oneill, Taryn
  • Webb, Michael I.
  • Vogels, Christopher M.
  • Bowes, Eric G.
  • Flewelling, Andrew
  • Gray, Christopher A.
  • Li, Haoxin
OrganizationsLocationPeople

article

Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities

  • Geier, Michael J.
  • Westcott, Stephen A.
  • Lee, Graham M.
  • Decken, Andreas
  • Oneill, Taryn
  • Webb, Michael I.
  • Vogels, Christopher M.
  • Bowes, Eric G.
  • Flewelling, Andrew
  • Gray, Christopher A.
  • Li, Haoxin
  • Halcovitch, Nathan Ross
Abstract

<p>A family of arylspiroborates has been prepared by the addition of either 4-tert-butylcatechol or 3,5-di-tert-butylcatechol to boric acid and an alkali metal hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on potassium (bis-(3,5-di-tertbutyl[1,2-benzenediolato(2-)-O,O]borate)) (8). All compounds displayed appreciable anti-microbial activities.</p>

Topics
  • compound
  • single crystal X-ray diffraction
  • single crystal
  • Potassium
  • Nuclear Magnetic Resonance spectroscopy