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Preparations, vibrational spectra, and Mössbauer spectra of tin(<scp>II</scp>) species of the types SnX<sub>3</sub><sup>–</sup>and SnX<sub>2</sub>Y<sup>–</sup>(X, Y = Cl, Br, or I)
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1970
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EngineeringSolid-state ChemistryChemistryInorganic MaterialSpectroscopic PropertySpectra-structure CorrelationSolid StateInorganic CompoundPyramidal AnionsMossbauer SpectroscopyMaterials ScienceInorganic ChemistryPhysical ChemistryQuantum ChemistryVibrational SpectraNitromethane SolutionNatural SciencesSpectroscopyCondensed Matter PhysicsMössbauer Spectra
A series of tin(II) salts of the types Et4N[SnX3] and Et4N[SnX2Y](X, Y = Cl, Br, or I) have been prepared, the latter for the first time. The salts are all sensitive to oxygen, their stability in this regard decreasing from SnCl3– to SnX2Y– to Snl3–. The i.r. and Raman spectra of the ions have been recorded both in the solid state and also where possible in nitromethane solution. There are signification differences between the data pertaining to the two states, and only in solution is it clear that discrete, pyramidal anions are present. The Mössbauer spectra of the salts yield isomer shifts in the range 3·47–3·95 mm./sec. relative to SnO2; the shifts for the SnX3– ions increase as the sums of the electronegativites of the attached halogen atoms decrease.