Mössbauer Spectra of Tris(diorganothioselenocarbamato)- and Tris(diorganodiselenocarbamato)iron(III) Complexes

Abstract

Room temperature 57Fe Mössbauer spectra of several tris(diorganothioselenocarbamato)- and tris(diorganodiselenocarbamato)iron(III) complexes are reported, along with their room temperature magnetic moments for the solid state. These results are compared to the previously reported diethyl derivatives and to the corresponding monothio- and dithiocarbamates. Each complex exhibited a single, quadrupole-split absorption in its Mössbauer spectrum. Although variations are noted within specific organic substituents, general trends for the average isomer shifts of all ligands are -OSCNR2 < -S2CNR2 ∼-SSeCNR2 ∼-Se2CNR2, while the typical order of the quadrupole splittings for a given ligand is -OSCNR2 < -S2CNR2 < -SSeCNR2 < -Se2CNR2. For the same organic substituent, the magnetic moments usually decrease in the order -OSCNR2 > -S2CNR2 > -SSeCNR2 > -Se2CNR2. It is noteworthy that higher quadrupole splittings are observed for the symmetric diselenocarbamate iron(III) complexes than for the corresponding thioselenocarbamates. © 1990.

Department(s)

Chemistry

International Standard Serial Number (ISSN)

0020-1693

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 1990 Elsevier, All rights reserved.

Publication Date

01 Jan 1990

Link to Full Text

Share

 
COinS