The nature of the bond between a metal and an unsaturated hydrocarbon is one of the most fundamental and significant problems in coordination chemistry. In spite of wide structural and spectroscopic studies of olephinic π-complexes a number of fundamental spectroscopic properties have not been clearified yet. Reinvestigation of FT-IR and Raman spectra of K[Pt(C 2 H 4)Cl 3 ] and K[Pt(C 2 H 4)Cl 3 ].H 2 0 in both the solid phase and water/HCl solution suggests some modification of widely accepted assignments. Skeletal modes of [NBu 4 ][Pt(C 2 H 4)Br 3 ], [NBu 4 ][Pd(C 2 H 4)Cl 3 ] and their C 2 D 4 derivatives have been measured and assigned. A new model for the normal coordinate treatment of π-complexes has been adopted to calculate metal-ligand force constants. © 1989 IUPAC
CITATION STYLE
Mink, J., Pápai, I., Gál, M., & Goggin, P. L. (1989). Recent Developments of FT-IR and Raman Spectroscopy in Coordination Chemistry. Pure and Applied Chemistry, 61(5), 973–978. https://doi.org/10.1351/pac198961050973
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