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 (2/2 displayed)

  • 2010The neutron diffraction study, calorimetry and spontaneous polarization of pyridinium perrhenate at 350, 300 and 100K4citations
  • 2006Structure, phase transitions and dielectric properties of a new inclusion compound of bis-thiourea pyridinium nitrate salt16citations

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Czarnecki, Piotr
2 / 18 shared
Cousson, Alain
1 / 5 shared
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2010
2006

Co-Authors (by relevance)

  • Czarnecki, Piotr
  • Cousson, Alain
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article

Structure, phase transitions and dielectric properties of a new inclusion compound of bis-thiourea pyridinium nitrate salt

  • Małuszyńska, Hanna
  • Czarnecki, Piotr
Abstract

<p>A structure of a new inclusion compound of bis-thiourea pyridinium nitrate salt C<sub>5</sub>H<sub>6</sub>N<sup>+</sup>NO<sub>3</sub><sup>-</sup> 2[CH <sub>4</sub>N<sub>2</sub>S] was determined by single-crystal X-ray diffraction method at 293 K, 250 K and 150 K. In high temperature phase the compound crystallizes in orthorhombic system, the two low-temperature phases are monoclinic. The sequence of phases is: Pbnm ⇒ P2<sub>1</sub>/c ⇒ P2<sub>1</sub>. In the orthorhombic form (I) the a axis is doubled in respect to the monoclinic forms and pyridinium and nitrate ions are partially disordered. Both low-temperature monoclinic phases (II) and (III) are ordered but twinned by pseudomerohedry. In all three phases the host lattice is built of ribbons of hydrogen-bonded thiourea molecules and nitrate anions forming channels in which the guests pyridinium cations are located. Each ribbon consists of two crystallographically independent thiourea molecules and nitrate ions. Four ribbons form a channel parallel to the c axis with approximately square cross-section. In the channel there is a stack of pyridinium cations, which planes form an inclination angle with the channel axis. The angle varies from about 90° in disordered phase I to 60° in well ordered phase (III). The dielectric spectroscopy measurements were performed on the polycrystalline sample with HP-4291A impedance analyser in the frequency range 1 MHz-1 GHz. The dielectric measurements reveal that two phase transitions occur at T<sub>1</sub> = 287 K and at T<sub>2</sub> = 217 K. The phase transition at T<sub>2</sub> = 287 K is of the first order with the thermal hysteresis of 10 K at cooling and heating. The phase transition at 217 K is of the second order and the dielectric anomaly suggests the ferroelectric-paraelectric phase transition. The dielectric relaxation observed below T<sub>2</sub> are caused by the pyridinium cation reorientation. The dielectric relaxation time changes with the temperature according to Arrhenius low and the activation energy of the relaxation process is about 14 kJ/mol. © by Oldenbourg Wissenschaftsverlag.</p>

Topics
  • impedance spectroscopy
  • compound
  • inclusion
  • x-ray diffraction
  • Hydrogen
  • phase transition
  • forming
  • activation
  • disordered phase
  • ordered phase
  • twinned
  • diffraction method