Chromium(III), manganese(II) and iron(III) O,O'-bonded complexes of the para- and meta-substituted benzeneseleninic acids

1980 ◽  
Vol 33 (6) ◽  
pp. 1203 ◽  
Author(s):  
C Preti ◽  
G Tosi

A number of complexes of chromium(III), manganese(II) and iron(III) with para- and meta-substituted benzeneseleninic acids, XC6H4SeO2H (X = H, p-Cl, m-Cl, p-Br, m-Br, p-Me), are reported. The newly prepared compounds are characterized on the basis of near-i.r. and far-i.r. spectroscopy, electronic spectra and conductivity measurements, as well as by magnetochemical evidence. The wavelengths of the principal absorption peaks have been accounted for quantitatively in terms of the crystal field theory for chromium(III) and manganese(II) derivatives. The nephelauxetic parameters are all indicative of an appreciable metal-ligand covalency. The i.r. spectral data suggest that the ligands act as bidentate in seleninato-O,O' complexes and we can propose octahedral geometries with D3 symmetry for the chromium(III) and iron(III) derivatives and octahedral geometries, distorted towards D4h, for the manganese(II) complexes, in which the water has been shown to be coordinated to the metal.

1985 ◽  
Vol 38 (11) ◽  
pp. 1675 ◽  
Author(s):  
G Graziosi ◽  
C Preti ◽  
G Tosi ◽  
P Zannini

New complexes of osmium(III) with para - and meta-substituted benzeneseleninic acids of the type XC6H4SeO2H (X = H, p- Cl , m- Cl , p-Br, m-Br, p-Me) are reported. The compounds, of the type Os(XC6H4SeO2)3, Os(XC6H4SeO2)2Y, Os(XC6H4SeO2)Y2 and Os2(XC6H4SeO2)3Y3 (Y = Cl , Br), have been studied through spectroscopic techniques ( i.r ., far- i.r .and electronic spectra), magnetic susceptibility measurements, thermogravimetric studies and conductivity measurements. The wavelengths of the principal electronic absorption peaks have been accounted for quantitatively in terms of the crystal-field theory; the nephelauxetic parameter is indicative of an appreciable metal- ligand covalency. It is worth noting that among the present complexes the highest q values are related to the Os(XC6H4SeO2)3 derivatives in which OsO6 chromophores are present; the Dq values decrease on passing to the 1 : 2, 1 : 1.5 and 1 : 1 metal/ ligand molar ratio complexes according to the presence of chlorine- and bromine-containing chromophores . The i.r . data point to a seleninato -O,O′ coordination for all the complexes; in particular, the presence of three SeO bands with the irreducible representation A2 + 2E in the i.r . spectra of the tris derivatives suggests an octahedral configuration with D3 symmetry. All the halo complexes are polymeric octahedral with bridging halide atoms. The magnetic moment values lie in the expected range for the trisbenzeneseleninato derivatives, and they decrease on passing to the halo complexes.


1996 ◽  
Vol 89 (5-6) ◽  
pp. 649-655
Author(s):  
R. Gupta ◽  
U.S. Ghosh ◽  
C. Basu

2019 ◽  
Vol 21 (4) ◽  
Author(s):  
M.G. Brik ◽  
◽  
N.M. Avram ◽  
C.N. Avram ◽  
◽  
...  

1972 ◽  
Vol 27 (11) ◽  
pp. 1672-1677 ◽  
Author(s):  
A. Gołębiewski ◽  
R. Nalewajski

Abstract The electronic structure of dodecahedral octacyanides of molybdenum IV and V is described in terms of SCCC molecular orbitals. Five MO's resemble d orbitals of the central atom. The splitting of appropriate levels is almost exactly the same as that following from the crystal field theory for G4/G2 ~ 0.7. According to the theory stable Mo(CN)84- is dodecahedral and stable MO(CN)83- is antiprismatic. In the dodecahedron the A-type ligands are bonded more strongly than the B-type ligands.


1967 ◽  
Vol 20 (2) ◽  
pp. 433-441 ◽  
Author(s):  
E. Jäger ◽  
R. Perthel

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