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Issue 21, 2014
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Equiatomic intermetallic compounds YTX (T = Ni, Ir; X = Si, Ge, Sn, Pb): a systematic study by 89Y solid state NMR and 119Sn Mössbauer spectroscopy

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Abstract

The equiatomic TiNiSi type tetrelides YTX (space group Pnma) with T = Ni, Ir and X = Si, Ge, Sn, Pb were synthesized from the elements by arc-melting or via high-frequency-melting of the elements in sealed niobium ampoules. All samples were characterized by powder X-ray diffraction using the Guinier technique. The structures of YNiGe, YNiPb, YIrSi, YIrGe, and YIrSn were refined from single crystal X-ray diffractometer data. The YTX tetrelides are characterized by a three-dimensional [TX] network that consists of puckered T3X3 hexagons with T–X distances in the order of the sums of the covalent radii. YIrSi and YIrGe show a reverse occupancy of the T and X sites with respect to the remaining YTX compounds, which is most likely a size effect. Solid state NMR studies reveal the sensitivity of 89Y Knight shifts to electronic structure details. A monotonic dependence on the tetrelide Pauling electronegativity is observed in addition. The stannides YTSn (T = Ni, Rh, Ir, Pt) were further characterized by 119Sn Mössbauer spectroscopy. They show single signals that are subjected to quadrupole splitting. Comparison of the isomer shifts with the whole series of YTSn stannides gives no hint of obvious correlations as a consequence of the valence electron count but reveals a systematic decrease with atomic number within a given group.

Graphical abstract: Equiatomic intermetallic compounds YTX (T = Ni, Ir; X = Si, Ge, Sn, Pb): a systematic study by 89Y solid state NMR and 119Sn Mössbauer spectroscopy

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Publication details

The article was received on 16 Jan 2014, accepted on 21 Feb 2014 and first published on 24 Feb 2014


Article type: Paper
DOI: 10.1039/C4DT00161C
Citation: Dalton Trans., 2014,43, 7860-7867
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    Equiatomic intermetallic compounds YTX (T = Ni, Ir; X = Si, Ge, Sn, Pb): a systematic study by 89Y solid state NMR and 119Sn Mössbauer spectroscopy

    C. Höting, H. Eckert, F. Haarmann, F. Winter and R. Pöttgen, Dalton Trans., 2014, 43, 7860
    DOI: 10.1039/C4DT00161C

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