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Far-infrared Spectra of Zinc Halide Complexes with Acetonitrile
12
Citations
22
References
1972
Year
Materials ScienceInorganic ChemistrySp2 Valency StatesEngineeringTheoretical Inorganic ChemistryZinc Halide ComplexesSpectroscopyNatural SciencesCoordination ComplexPhysical ChemistryMolecular ComplexChemistryNitrogen DonorsInorganic Compound
Abstract The infrared spectra of zinc halide complexes with acetonitrile, ZnX2·2CH3CN (X=Cl, Br, I), in the solid state were recorded in the region from 4000 to 96 cm−1. The Zn–N stretching bands for the chloride and bromide were observed, at 210 and 212 cm−1 respectively, as composite bands of the A1 and B1 species. For the iodide, the Zn–N stretching band of the B1 species was observed at 219 cm−1, while the A1 mode was coupled with the Zn–I stretching mode and was absorbed at 252 and 179 cm−1. The N–Zn–N bending bands were observed at 163, 162, and 153 cm−1 and the Zn–N≡C bending bands, at 125, 128, and 132 cm−1, for the chloride, bromide, and iodide respectively. The normal coordinate analysis was carried out by the use of the Urey-Bradley force field, and the Zn–N stretching force constant was obtained as 0.56 mdyn/Å. The force constant is much smaller than the corresponding ones in complexes containing nitrogen donors in the sp3 and the sp2 valency states.
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