Laura Voigt

ORCID: 0000-0001-9967-4061
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Magnetism in coordination complexes
  • Metal-Organic Frameworks: Synthesis and Applications
  • Lanthanide and Transition Metal Complexes
  • Layered Double Hydroxides Synthesis and Applications
  • Metal complexes synthesis and properties
  • Magnesium Oxide Properties and Applications
  • 2D Materials and Applications
  • Asymmetric Hydrogenation and Catalysis
  • Organic and Molecular Conductors Research
  • Organometallic Complex Synthesis and Catalysis
  • Molten salt chemistry and electrochemical processes
  • Perovskite Materials and Applications
  • Metal-Catalyzed Oxygenation Mechanisms
  • CO2 Reduction Techniques and Catalysts
  • Material Properties and Applications
  • Metallurgical Processes and Thermodynamics
  • Crystallography and molecular interactions
  • Nuclear Materials and Properties
  • Chemical Reactions and Mechanisms
  • Quasicrystal Structures and Properties
  • Machine Learning in Materials Science
  • Electron Spin Resonance Studies
  • Nanocluster Synthesis and Applications

Technical University of Denmark
2018-2024

Joint Research Centre
2024

University of Copenhagen
2020-2022

University of the Basque Country
2021

University of Aveiro
2021

Osaka University
2021

Ikerbasque
2021

Electronic synergy between metal ions and organic linkers is a key to engineering molecule-based materials with high electrical conductivity and, ultimately, metallicity. To enhance in metal-organic solids, chemists aim bring the electrochemical potentials of constituent bridging ligands closer quest obtain metal-d ligand-π admixed frontier bands. Herein, we demonstrate critical role ion tuning electronic ground state such materials. While VCl2(pyrazine)2 an insulator, TiCl2(pyrazine)2...

10.1038/s41467-022-33342-5 article EN cc-by Nature Communications 2022-09-30

Bespoke van der Waals (vdW) crystals provide control over the generation, confinement, and transport of charge, spin, light, heat within between atomically precise two-dimensional (2D) layers. We report a novel functionality in vdW by actuating valence changes metal-organic antiferromagnet through molecular alloying. The quadratic net materials Cr(pyz)2Br2 Cr(pyz)2I2 (pyz = pyrazine) are aliovalent, with different Cr(III) Cr(II) oxidation states due to disparate crystal field potentials...

10.26434/chemrxiv-2024-rlsf8 preprint EN 2024-07-22

Group 6 metal hexacarbonyl complexes are employed as building blocks for pyrazine-pillared metal–organic frameworks with zero-valent centres.

10.1039/d1cc00864a article EN Chemical Communications 2021-01-01

The self-assembly of lanthanide ions with ditopic organic spacers results in the formation complex tiling patterns that mimic structural motifs quasi-periodic 2D materials. linking trans-{LnI2}+ nodes (Ln = Gd, Dy) by both closed-shell and anion radicals 4,4′-bipyridine affords rare examples Archimedean tessellations a metal–organic framework. We furthermore demonstrate occurrence sizable magnetic exchange interactions slow relaxation magnetization behavior tessellation pattern....

10.1021/jacs.1c05057 article EN Journal of the American Chemical Society 2021-08-10

β-Diketonates, such as acetylacetonate, are amongst the most common bidentate ligands towards elements across entire periodic table and considered wholly redox-inactive in their complexes. Herein we show that complexation of 1,1,1,5,5,5-hexafluoroacetylacetonate (hfac- ) to CrII spontaneously affords CrIII a reduced β-diketonate radical ligand scaffold, evidenced by crystallographic analysis, magnetic measurements, optical spectroscopy, reactivity studies, DFT calculations. The possibility...

10.1002/chem.201904899 article EN Chemistry - A European Journal 2019-11-13

Tailoring the chemical surroundings of chromium(<sc>ii</sc>) allows reversible electron-transfer to ubiquitous, purportedly redox-inactive acetylacetonate.

10.1039/d0sc01836h article EN cc-by-nc Chemical Science 2020-01-01

Abstract Tessellation of self-assembling molecular building blocks is a promising strategy to design metal-organic materials exhibiting geometrical frustration and ensuing frustrated physical properties. Appearing in two-dimensional quasiperiodic phases, tilings consisting five-vertex nodes are regarded as approximants for quasicrystals. Unfortunately, these structural motifs exceedingly rare due the complications acquiring five-fold coordination confined plane. Lanthanide ions display...

10.1038/s41467-020-18328-5 article EN cc-by Nature Communications 2020-09-17

Layered double hydroxides (LDHs) occur naturally and are synthesized for catalysis, drug delivery, contaminant remediation. They consist of Me(II)–Me(III) hydroxide sheets separated by hydrated interlayers weakly held anions. Often, LDHs nanocrystalline, sheet stacking arrangement can be disordered, which influences the reactivity complicates structural characterization. We have used pair distribution function (PDF) analysis to provide detailed information about local medium range order (≤9...

10.1021/acsearthspacechem.1c00293 article EN ACS Earth and Space Chemistry 2022-01-18

General interest in the deployment of molten salt reactors (MSRs) is growing, while available data on uranium-containing fuel candidates remains scarce. Thermophysical are one key parameters for reactor design and understanding operability. Hence, filling gap missing crucial to allow advancement MSRs. This study provides novel two eutectic compositions within NaF-KF-UF4 ternary system which serve as potential Experimental measurements include their melting point, density, fusion enthalpy,...

10.3390/ma17112776 article EN Materials 2024-06-06

The self-assembly of trivalent lanthanide ions with ditopic organic spacers results in the formation complex tiling patterns that mimic structural motifs quasi-periodic 2D materials. assembly trans -{LnI 2 } + nodes (Ln = Gd, Dy) both closed-shell and anion radicals 4,4'-bipyridine affords rare examples Archimedean tessellations a metal-organic framework. We furthermore demonstrate occurrence sizable magnetic exchange interactions slow relaxation magnetization behaviour tessellation pattern....

10.26434/chemrxiv.14529090.v1 preprint EN cc-by-nc-nd 2021-05-05

Layered double hydroxides (LDHs) occur naturally and are synthesised for catalysis, drugdelivery contaminant remediation. They consist of Me(II)-Me(III) hydroxide sheetsseparated by hydrated interlayers weakly held anions. Often, LDHs nanocrystalline andsheet stacking arrangement can be disordered, which influence reactivity andcomplicate structural characterisation. We have used pair distribution function (PDF) analysis, toprovide detailed information about local medium range order (&lt; 9...

10.26434/chemrxiv.11925507.v1 preprint EN cc-by-nc-nd 2020-03-04

The quest for simple ligands to participate in concerted base metal-ligand multiple-electron redox events is driven by perspectives of replacing noble metals catalysis and discovering novel chemical reactivity. Yet the vast majority ligand systems displays electrochemical potentials impractical catalytic cycles substantiating importance new strategies towards aligned metal–ligand orbital energy levels. We herein demonstrate possibility establish tame elusive non-innocence ubiquitous...

10.26434/chemrxiv.12052884.v1 preprint EN cc-by-nc-nd 2020-04-01

&lt;div&gt;Layered double hydroxides (LDHs) occur naturally and are synthesised for catalysis, drug&lt;/div&gt;&lt;div&gt;delivery contaminant remediation. They consist of Me(II)-Me(III) hydroxide sheets&lt;/div&gt;&lt;div&gt;separated by hydrated interlayers weakly held anions. Often, LDHs nanocrystalline and&lt;/div&gt;&lt;div&gt;sheet stacking arrangement can be disordered, which influence reactivity and&lt;/div&gt;&lt;div&gt;complicate structural characterisation. We have used pair...

10.26434/chemrxiv.11925507 preprint EN cc-by-nc-nd 2020-03-04

&lt;p&gt;The quest for simple ligands to participate in concerted base metal-ligand multiple-electron redox events is driven by perspectives of replacing noble metals catalysis and discovering novel chemical reactivity. Yet the vast majority ligand systems displays electrochemical potentials impractical catalytic cycles substantiating importance new strategies towards aligned metal–ligand orbital energy levels. We herein demonstrate possibility establish tame elusive...

10.26434/chemrxiv.12052884 preprint EN cc-by-nc-nd 2020-04-01
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