Abstract
The FT-IR and FT-Raman spectra of the tetranuclear Bi(III) complex Bi(C5H5NH)6Bi4Cl18 are investigated. The spectroscopic data reflect the non-equivalence of the pyridinium ions and suggest a strong distortion of the octahedral structure for the Bi4Cl18 group. The near-infrared data show that like in the fundamental region, protonation of pyridine results in a frequency increase of several combination bands.