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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Persson, Ingmar

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Swedish University of Agricultural Sciences

in Cooperation with on an Cooperation-Score of 37%

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Publications (18/18 displayed)

  • 2020Solution chemistry in the surface region of aqueous solutions1citations
  • 2019Chemical equilibria of aqueous ammonium-carboxylate systems in aqueous bulk, close to and at the water-air interface13citations
  • 2016Self-assembled SnO2 micro- and nanosphere-based gas sensor thick films from an alkoxide-derived high purity aqueous colloid precursor14citations
  • 2015The structures of CyMe4-BTBP complexes of americium(III) and europium(III) in solvents used in solvent extraction, explaining their separation properties40citations
  • 2015The structures of CyMe4-BTBP complexes of americium(III) and europium(III) in solvents used in solvent extraction, explaining their separation properties40citations
  • 2014Speciation and structure of lead(II) in hyper-alkaline aqueous solution11citations
  • 2012Crystal Structures of [Hg10(dmso)16](ClO4)10 and [Hg2(H2O)2](ClO4)22citations
  • 2010Structural Study of the N,N’-Dimethylpropyleneurea Solvated Lanthanoid(III) Ions in Solution and Solid State with an Analysis of the Ionic Radii of Lanthanoid(III) Ions74citations
  • 2008Fenton-Induced Degradation of Polyethylene Glycol and Oak Cellulose. A Model Experiment in Comparison to Changes Observed in Conserved Waterlogged Wood38citations
  • 2008Structure of solvated mercury(II) halides in liquid ammonia, triethyl phosphite and tri-n-butylphosphine solution8citations
  • 2007X-Ray Absorption Fine Structure Spectroscopic Studies of Octakis-(dimethylsulfoxide)lanthanoid(III) Complexes in Solution and in the Solid Iodides27citations
  • 2006Crystal Structure of Lead(II) Acetylacetonate and the Structure of the Acetylacetone Solvated Lead(II) Ion in Solution Studied by Large Angle X-ray scattering19citations
  • 2004Structure of the Hydrated, Hydrolysed and Solvated Zirconium(IV) and Hafnium(IV) Ions in Water and Aprotic Oxygen Donor Solvents. A Crystallographic, EXAFS Spectroscopic and Large Angle X-ray Scattering Study98citations
  • 2003Dimethyl Sulfoxide Solvates of the Aluminium(III), Gallium(III) and Indium(III) Ions30citations
  • 2003A Structural Study of the Hydrated and the Dimethylsulfoxide, N,N’-Dimethyl-propyleneurea, Acetonitrile, Pyridine and N,N-Dimethylthioformamide Solvated Nickel(II) Ion Solution and Solid Statecitations
  • 2003The discovery of the N,N-dimethylthioformamidium ion. A structural study of {(CH3)2NCHSH)}2[HfCl6] in solid state and solution7citations
  • 2001New Class of Oligonuclear Platinum-Thallium Compounds with a Direct Metal-Metal Bond. 5. Structure of Heterodimetallic Cyano Complexes in Aqueous Solution by EXAFS and Vibrational Spectroscopy36citations
  • 2001Crystal and Solution Structures of N,N-Dimethylthioformamide-Solvated Copper(I), Silver(I), and Gold(I) Ions Studied by X-ray Diffraction, X-ray Absorption, and Vibrational Spectroscopy22citations

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Björneholm, Olle
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Werner, Josephina
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Bajnoczi, Eva G.
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Blanco, Yina Salamanca
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Topel, Önder
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Topel, Onder
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Lundberg, Daniel
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Ekberg, Christian
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Geist, Andreas
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Aneheim, Emma
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Löfström-Engdahl, Elin
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Denecke, Melissa
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Co-Authors (by relevance)

  • Björneholm, Olle
  • Werner, Josephina
  • Bajnoczi, Eva G.
  • Blanco, Yina Salamanca
  • Topel, Önder
  • Topel, Onder
  • Lundberg, Daniel
  • Ekberg, Christian
  • Geist, Andreas
  • Aneheim, Emma
  • Löfström-Engdahl, Elin
  • Denecke, Melissa
  • Foreman, Mark R. Stj.
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article

New Class of Oligonuclear Platinum-Thallium Compounds with a Direct Metal-Metal Bond. 5. Structure of Heterodimetallic Cyano Complexes in Aqueous Solution by EXAFS and Vibrational Spectroscopy

  • Persson, Ingmar
Abstract

The structures of three closely related heterodimetallic cyano complexes, [(NC)5Pt−Tl(CN)n]n- (n = 1−3), formed in reactions between [PtII(CN)4]2- and TlIII cyano complexes, have been studied in aqueous solution. Multinuclear NMR data (205Tl, 195Pt, and 13C) were used for identification and quantitative analysis. X-ray absorption spectra were recorded at the Pt and Tl LIII edges. The EXAFS data show, after developing a model describing the extensive multiple scattering within the linearly coordinated cyano ligands, short Pt−Tl bond distances in the [(NC)5Pt−Tl(CN)n]n- complexes:  2.60(1), 2.62(1), and 2.64(1) Å for n = 1−3, respectively. Thus, the Pt−Tl bond distance increases with increasing number of cyano ligands on the thallium atom. In all three complexes the thallium atom and five cyano ligands, with a mean Pt−C distance of 2.00−2.01 Å, octahedrally coordinate the platinum atom. In the hydrated [(NC)5Pt−Tl(CN)(H2O)4]- species the thallium atom coordinates one cyano ligand, probably as a linear Pt−Tl−CN entity with a Tl−C bond distance of 2.13(1) Å, and possibly four loosely bound water molecules with a mean Tl−O bond distance of about 2.51 Å. In the [(NC)5Pt−Tl(CN)2]2- species, the thallium atom probably coordinates the cyano ligands trigonally with two Tl−C bond distances at 2.20(2) Å, and in [(NC)5Pt−Tl(CN)3]3- Tl coordinates tetrahedrally with three Tl−C distances at 2.22(2) Å. EXAFS data were reevaluated for previously studied mononuclear thallium(III)−cyano complexes in aqueous solution, [Tl(CN)2(H2O)4]+, [Tl(CN)3(H2O)], and [Tl(CN)4]-, and also for the solid K[Tl(CN)4] compound. A comparison shows that the Tl−C bond distances are longer in the dinuclear complexes [(NC)5Pt−Tl(CN)n]n- (n = 1−3) for the same coordination number. Relative oxidation states of the metal atoms were estimated from their 195Pt and 205Tl chemical shifts, confirming that the [(NC)5Pt−Tl(CN)n]n- complexes can be considered as metastable intermediates in a two-electron-transfer redox reaction from platinum(II) to thallium(III). Vibrational spectra were recorded and force constants from normal-coordinate analyses are used for discussing the delocalized bonding in these species.

Topics
  • compound
  • Platinum
  • Nuclear Magnetic Resonance spectroscopy
  • quantitative determination method
  • vibrational spectroscopy
  • extended X-ray absorption fine structure spectroscopy
  • Thallium