Spectroscopic characterization of anionic tris(N,N-dialkyldithiocarbamate) complexes of zinc(II) and cadmium(II)
The infrared and Raman spectra (1500-50 cm-1) of the related complexes Zn(S2CNMe2)2(I), [Bu4N][Zn(S2CNMe2)3] (II), Cd(S2CNMe2)2 (III), [Bu4N][Cd(S2CNMe2)3](IV), Cd(S2CNEt2)2(V) and [Bu4N][Cd(S2CNEt2)3] (VI) have been determined. For complexes with coordination number four, metalsulfur stretching fre...
Publicado: |
1989
|
---|---|
Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00201693_v164_n2_p149_Frigerio http://hdl.handle.net/20.500.12110/paper_00201693_v164_n2_p149_Frigerio |
Aporte de: |
Sumario: | The infrared and Raman spectra (1500-50 cm-1) of the related complexes Zn(S2CNMe2)2(I), [Bu4N][Zn(S2CNMe2)3] (II), Cd(S2CNMe2)2 (III), [Bu4N][Cd(S2CNMe2)3](IV), Cd(S2CNEt2)2(V) and [Bu4N][Cd(S2CNEt2)3] (VI) have been determined. For complexes with coordination number four, metalsulfur stretching frequencies were assigned at 228 cm-1 for I (ZnS), 180 cm-1 for III (CdS) and 208 cm-1 for V (CdS), whereas for complexes with apparent coordination number six they were assigned at 206 cm-1 for II (ZnS) and in the 150-125 cm-1 range for IV and VI (CdS). Thus, expansion of the coordination sphere of the Zn(II) and Cd(II) metal results in a significant shift towards lower energy of the far IR MS vibrations. Other MS sensitive vibrations in the far IR are found in the 385-350 cm-1 range, and are described as mixed ring bending modes with significant MS stretching contribution. © 1989. |
---|