Materials Map

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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 (1/1 displayed)

  • 2022Heterometallic {Fe18M6} (M = Y, Gd, Dy) pivalate wheels display solvent-induced polymorphism7citations

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Chart of shared publication
Podgornii, Daniel
1 / 1 shared
Öhrström, Lars
1 / 5 shared
Baca, Svetlana G.
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Noa, Francoise M. Amombo
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Mckenzie, Christine
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Kögerler, Paul
1 / 6 shared
Chart of publication period
2022

Co-Authors (by relevance)

  • Podgornii, Daniel
  • Öhrström, Lars
  • Baca, Svetlana G.
  • Noa, Francoise M. Amombo
  • Mckenzie, Christine
  • Kögerler, Paul
OrganizationsLocationPeople

article

Heterometallic {Fe18M6} (M = Y, Gd, Dy) pivalate wheels display solvent-induced polymorphism

  • Podgornii, Daniel
  • Öhrström, Lars
  • Baca, Svetlana G.
  • Noa, Francoise M. Amombo
  • Mckenzie, Christine
  • Kögerler, Paul
  • Leusen, Jan Van
Abstract

<p>A new series of heterometallic wheels, isolated as [Fe18M6(piv)12(Htea)18(tea)6(N3)6]·n(solvent) (MIII = Y (1a, 1b), Gd (2a, 2b), and Dy (3a, 3b); Hpiv = pivalic acid, H3tea = triethanolamine), forms by the reaction of trinuclear μ3-oxo-linked or hexanuclear μ-OH-linked Fe(III) pivalate clusters with rare earth nitrates, H3tea, and azide ligands in MeOH/MeCN or EtOH/MeCN media under ultrasonic irradiation. Single-crystal X-ray diffraction showed that wheels 1a-3a prepared from MeOH/MeCN solutions crystallize in the triclinic space group P1¯ and have Ci symmetry, whereas wheels 1b-3b received from EtOH/MeCN solution crystallize in the trigonal space group R3¯ and have C3i symmetry. Magnetic studies reveal medium antiferromagnetic exchange interactions within the Fe3 trimeric unit (with the exchange coupling parameters of JFe3 = -13.1 cm-1 for 1a, JFe3 = -11.6 cm-1 for 1b) and weak intermolecular antiferromagnetic exchange interactions (λmf = -0.366 mol cm-3 and -0.368 mol cm-3 (zJmf = -0.19 cm-1), respectively). This leads to spin ground states of S = 5/2 for each {Fe3} unit. Substitution of diamagnetic Y(III) centers by paramagnetic Ln(III) centers (in 2a/2b by Gd(III) and in 3a/3b by Dy(III) centers) results in ferromagnetic exchange interactions between the Fe(III) and Ln(III) centers in addition to the predominant antiferromagnetic Fe···Fe interactions in 1a/1b.</p>

Topics
  • cluster
  • x-ray diffraction
  • ultrasonic
  • chemical ionisation
  • space group