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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University of York

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2021Synthesis and mesomorphism of related series of triphilic ionic liquid crystals based on 1,2,4-triazolium cations16citations
  • 2015Spin-crossover, mesomorphic and thermoelectrical properties of cobalt(II) complexes with alkylated N3-Schiff bases18citations
  • 2008Metal-directed columnar phase formation in tetrahedral zinc(II) and manganese(II) metallomesogens21citations
  • 2008Design of Neutral Metallomesogens from 5,5-Dimethyldipyrromethane: Metal Ion Mediated Control of Folding and Hairpin Structures20citations
  • 2007Liquid-crystalline complexes of 1,10-phenanthrolinecitations
  • 2001Mesomorphic complexes of the lanthanide elements9citations
  • 2000Rare-earth-containing magnetic liquid crystalscitations

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Chart of shared publication
Slattery, John M.
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Rogers, Sarah E.
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Pibiri, Ivana
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Riccobono, Alessio
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Pace, Andrea
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Lazzara, Giuseppe
1 / 23 shared
Macfarlane, Douglas
1 / 33 shared
Donnio, Bertrand
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Heinrich, Benoit
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Schroder, Martin
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Blake, Alexander J.
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Collinson, Simon
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Morale, Francesca
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Finn, Rachel L.
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Wilson, Claire
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Guillon, Daniel
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Love, Jason B.
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Ames, Kelly A.
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Schröder, Martin
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Ramaekers, Jan
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Cardinaels, Thomas
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Collinson, Simon R.
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Martin, Françoise
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Deun, Rik Van
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Galyametdinov, Yury G.
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2015
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Co-Authors (by relevance)

  • Slattery, John M.
  • Rogers, Sarah E.
  • Pibiri, Ivana
  • Riccobono, Alessio
  • Pace, Andrea
  • Lazzara, Giuseppe
  • Macfarlane, Douglas
  • Donnio, Bertrand
  • Lazar, Manoj Ainikalkannath
  • Heinrich, Benoit
  • Abdullah, Norbani Binti
  • Halcrow, Malcolm A.
  • Nordin, Abdul Rahman
  • Noor, Nur Linahafizza Md
  • Schroder, Martin
  • Blake, Alexander J.
  • Collinson, Simon
  • Morale, Francesca
  • Finn, Rachel L.
  • Wilson, Claire
  • Guillon, Daniel
  • Love, Jason B.
  • Ames, Kelly A.
  • Schröder, Martin
  • Binnemans, Koen
  • Ramaekers, Jan
  • Cardinaels, Thomas
  • Collinson, Simon R.
  • Martin, Françoise
  • Deun, Rik Van
  • Galyametdinov, Yury G.
OrganizationsLocationPeople

article

Design of Neutral Metallomesogens from 5,5-Dimethyldipyrromethane: Metal Ion Mediated Control of Folding and Hairpin Structures

  • Blake, Alexander J.
  • Donnio, Bertrand
  • Collinson, Simon
  • Bruce, Duncan W.
  • Love, Jason B.
  • Ames, Kelly A.
  • Schröder, Martin
  • Wilson, Claire
  • Guillon, Daniel
Abstract

New ligands derived from 5,5-dimethyldipyrromethane and their corresponding neutral complexes with Zn(II) and Pd(II) are described. The ligands incorporate either hexacatenar[H<sub>2</sub>(1<sup>n</sup>), n = 1, 10, 12, 14 and 16], tetracatenar [H<sub>2</sub>(2<sup>n</sup>), n = 1 and 16] or an extended dicatenar structure [H<sub>2</sub>(3<sup>n</sup>), n = 1 and 16].Single crystal X-ray structure determinations on [Zn<sub>2</sub>(1<sup>1</sup>)<sub>2</sub>] and [Zn<sub>2</sub>(3<sup>1</sup>)<sub>2</sub>] confirm a distorted tetrahedral geometry at Zn(II) to afford double-stranded helical structures, while the Pd(II) species [Pd(3<sup>1</sup>)] shows a distorted square planar geometry with the ligand adopting an alternative hairpin conformation.The metal-free hexacatenar ligands H<sub>2</sub>(1<sup>n</sup>) (n = 10, 12, 14, 16) and the corresponding complexes [Zn<sub>2</sub>(1<sup>16</sup>)<sub>2</sub>] and [Pd(1<sup>n</sup>)] (n = 12, 14, 16) are not mesomorphic.However, the tetracatenar complex [Zn<sub>2</sub>(2<sup>16</sup>)<sub>2</sub>] generates a smectic mesophase, as confirmed by X-ray diffraction, while [Pd(2<sup>16</sup>)] and the metal-free ligand H<sub>2</sub>(2<sup>16</sup>) show no mesomorphic behaviour.Two of the extended dicatenar compounds, H<sub>2</sub>(3<sup>16</sup>) and [Zn<sub>2</sub>(3<sup>16</sup>)<sub>2</sub>] are non-mesomorphic, while[Pd(3<sup>16</sup>)] displays a smectic A phase.

Topics
  • compound
  • single crystal
  • phase
  • x-ray diffraction