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)

  • 2014Facile Preparation of Mn3O4 Hausmanite Nanoplates from a New Octahedral Manganese (III) Schiff Base Complex4citations
  • 2013Spin crossover (SCO) iron(II) coordination polymer chain: Synthesis, structural and magnetic characterizations of [Fe(abpt)2(μ-M(CN)4)] (M=PtII and NiII)26citations

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Das, Debasis
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Nikookar, Mahsa
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Houille, Sylvie
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Setifi, Fatima
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2014
2013

Co-Authors (by relevance)

  • Das, Debasis
  • Nikookar, Mahsa
  • Thétiot, Franck
  • Khalaji, Aliakbar Dehno
  • Triki, Smail
  • Pillet, Sébastien
  • Houille, Sylvie
  • Setifi, Fatima
  • Gómez-García, Carlos J.
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article

Spin crossover (SCO) iron(II) coordination polymer chain: Synthesis, structural and magnetic characterizations of [Fe(abpt)2(μ-M(CN)4)] (M=PtII and NiII)

  • Pillet, Sébastien
  • Houille, Sylvie
  • Setifi, Fatima
  • Charles, Catherine
  • Thétiot, Franck
  • Gómez-García, Carlos J.
  • Triki, Smail
Abstract

New iron(II) coordination polymeric neutral chain of formula [Fe(abpt)2(μ-M(CN)4)], with M = PtII (1), NiII (2) and abpt = 4-amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole, have been synthesized and characterized by infrared spectroscopy, X-ray diffraction and magnetic measurements. The two compounds are isostructural as deduced from a Rietveld analysis of X-ray powder diffraction data of 2 simulated from the single crystal structure of 1. The crystal packing of 1 is formed by regular chains running along the crystallographic [−1 0 1] direction where the planar [Pt(CN)4]2− anion acts as a μ2-bridging ligand via two nitrogen atoms of two different trans cyano groups, while the two abpt molecules act as chelating ligands. Along the neutral chains, the Fe⋯Pt distances are imposed by the cyano groups of the [Pt(CN)4]2− moiety (5.027 and 5.022 Å at 294 and 150 K, respectively), leading to Fe⋯Fe intrachain distances of 10.055 and 10.045 Å at 294 and 150 K, respectively. The thermal dependence of the product of the molar magnetic susceptibility times the temperature (χmT) for compound 1 shows a constant value close to 0.2 emu K mol−1 in the temperature range 10–300 K in the cooling and warming scans. Above 300 K, compound 1 shows a SCO transition from the LS to the HS configuration although the transition is not fully achieved at 400 K.

Topics
  • impedance spectroscopy
  • compound
  • polymer
  • single crystal
  • x-ray diffraction
  • Nitrogen
  • iron
  • susceptibility
  • laser sintering
  • infrared spectroscopy