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Covalency of Neptunium(IV) organometallics from /sup 237/Np Moessbauer spectra

Conference ·
OSTI ID:5541584
The isomer shifts in /sup 237/Np Moessbauer spectra arise from the shielding of neptunium's 6s orbitals by the inner 5f orbitals. In covalent bonding, ligand contributions to the 5f electron density increase the shielding, and the /sup 237/Np isomer shift reflects differences in bond character among covalently bonded ligands. The large difference in isomer shift (3.8 cm/sec) between ionic Np(IV) and Np(III) compounds permits a good determination of ligand bonding differences in Np(IV) organometallic compounds. The Moessbauer spectra for about 20 Np(IV) organometallic compounds, principally cyclopentadienyl (Cp) compounds of the general composition Cp/sub x/Np chi/sub 4-x/ (x = 1,2,3; chi = Cl, BH/sub 4/, /sup n/Bu, Ph, OR, acac), show both the differences in sigma bonding among the chi ligands, as well as the covalent effect of the Cp ligands.
Research Organization:
Du Pont de Nemours (E.I.) and Co., Aiken, SC (USA). Savannah River Lab.
DOE Contract Number:
EY-76-C-09-0001
OSTI ID:
5541584
Report Number(s):
DP-MS-79-93; CONF-800303-8
Country of Publication:
United States
Language:
English