Relation of isomeric shift and quadrupole splitting in M�ssbauer spectra to electronic structure for the iron atom

1968 ◽  
Vol 2 (4) ◽  
pp. 382-386 ◽  
Author(s):  
V. I. Gol'danskii ◽  
E. F. Makarov ◽  
R. A. Stukan

Author(s):  
Nikolay G. Maksimov ◽  
Victor V. Verpekin ◽  
Dmitry V. Zimonin ◽  
Galina V. Burmakina ◽  
Oleg S. Chudin ◽  
...  

The chemical oxidation of the cluster CpReFePt(μ3-C=CHPh)(CO)5(dppe) (Cp = η5-C5H5, dppe = η2- Ph2P(CH2)2PPh2) resulted in a radical cation [CpReFePt(μ3-C=CHPh)(CO)5(dppe)]+• that is sufficiently stable only at low temperature. An electronic structure of the radical cation was studied by EPR and following parameters were obtained by comparison of the experimental and model spectrum: gx = 2.070 gy = 2.0295 gz = 1.997; Ax(31P) = 17 Ay(31P) = 49 Az(31P) = 35 (Gs);Ax(195Pt) = 62 Ay(195Pt) = 45 Az(195Pt) = 105 (Gs). An unpaired electron is seen to be mainly concentrated on the iron atom (85-90%) and partially on the platinum atom (10-15%). Further transformation of the radical cation led to the formation of the binuclear complex Cp(CO)2RePt(μ-C=CHPh)(dppe) and the Fe-carbonyl fragment



1996 ◽  
Vol 51 (5-6) ◽  
pp. 381-388 ◽  
Author(s):  
M. I. Oshtrakh

Abstract This review deals with studies of the variations of quadrupole splitting, electronic structure and stereochemistry of iron associated with qualitative changes of biomolecules. The possibility to determine various iron containing species resulting from the destruction of biomolecules using Mössbauer parameters is shown. A small change of iron stereochemistry leads to a small change of the iron electronic structure which could be detected by small changes of quadrupole splitting. It is expected that quadrupole splitting of iron gives new information for biomedical research on a molecular level.



2011 ◽  
Vol 66 (5) ◽  
pp. 441-443
Author(s):  
Constantin Hoch ◽  
Inga Schellenberg ◽  
Rainer Pöttgen

57Fe Mössbauer spectroscopic studies have shown that in cesium suboxoferrate, Cs9FeO4, the iron atom has the formal oxidation state +III. The isomer shift δ = 0.10(1) is in very good agreement with that of a large number of ionic ferrates(III). The same holds for geometrical details of the [FeO4]5− anion, which shows only a small deviation from ideal tetrahedral symmetry giving rise to a quadrupole splitting of ΔEQ = 0.36(2) mm/s



1980 ◽  
Vol 22 (11) ◽  
pp. 5128-5134 ◽  
Author(s):  
M. Braga ◽  
A. R. Riego ◽  
J. Danon


1963 ◽  
Vol 5 (3) ◽  
pp. 217-220 ◽  
Author(s):  
H. De Waard ◽  
G. De Pasquali ◽  
D. Hafemeister


1981 ◽  
Vol 11 (7) ◽  
pp. 1423-1433 ◽  
Author(s):  
A Rodriquez ◽  
J Keller


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