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   <subfield code="a">Far infrared spectra (500-50 cm−1) of the 2,2′-bipyridine complexes of palladium and platinum halides</subfield>
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   <subfield code="c">[Carola Engelter, David Thornton]</subfield>
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   <subfield code="a">Summary: The far-i.r. spectra of the title complexes have been examined. Band assignments are based on the shifts induced by ligand deuteration and halide substitution. Deuteration of bipyridine causes large shifts (Δν &gt;10 cm−1) in internal ligand modes, intermediate shifts Δν between 2 and 9 cm−1) in metal-nitrogen stretching and bending modes and small to zero shifts in metal-halide stretching and bending vibrations. Generally, the requirements for square planarC 2v synanetry [two ν(M−N) and two ν(M−X) bands] are observed. Previous ambiguities in the assignment of the ν(M−N) bands have been resolved by the isotopic labelling technique employed in this study.</subfield>
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