scholarly journals The Correlation between Reflectance Spectra and Magnetic Moments of Copper(II) Halide Complexes with PyridineN-Oxides

1967 ◽  
Vol 40 (7) ◽  
pp. 1738-1738 ◽  
Author(s):  
Michinobu Kato ◽  
Yoneichiro Muto ◽  
Hans B. Jonassen
1969 ◽  
Vol 42 (2) ◽  
pp. 417-431 ◽  
Author(s):  
Yoneichiro Muto ◽  
Michinobu Kato ◽  
Hans B. Jonassen ◽  
Louis Chopin Cusachs

1967 ◽  
Vol 40 (6) ◽  
pp. 1535-1536 ◽  
Author(s):  
Yoneichiro Muto ◽  
Michinobu Kato ◽  
Hans B. Jonassen ◽  
H. N. Ramaswamy

1976 ◽  
Vol 54 (15) ◽  
pp. 2426-2431 ◽  
Author(s):  
Giuseppe Marcotrigiano ◽  
Ledi Menabue ◽  
Gian Carlo Pellacani

The neutral six-coordinated tetragonal Co(β-ala)2•2H2O complex(β-ala = NH2CH2CH2COO−) was prepared. In this complex β-alanine acts as an O,N-chelating agent, as in the known Cu(β-ala)2•6H2O and Ni(β-ala)2•3H2O complexes. We also prepared some complexes of a type that is new for β-alanine, with stoichiometries such as M(β-alaH)2X2, M(β-alaH)4(ClO4)2 (M = Co and Ni), Cu(β-alaH)3(ClO4)2, and Cu(β-alaH)Cl2[Formula: see text] in which the ligand acts as a zwitterion and coordinates toward the carboxy group as a formally neutral ligand. The possibility of formulating the complexes as H2[M(β-ala)2X2] is discussed. The electronic spectra and the magnetic moments of the halide complexes are in accord with pseudo-tetrahedral, octahedral, and tetragonal stereochemistry for the cobalt(II), nickel(II), and copper(II) ions, respectively, while those of the perchlorate complexes are in accord with pseudooctahedral stereochemistry. The β-alanine hydrohalide salts and the bis(β-alaninium)tetrachlorocuprate complex were also prepared and are discussed.


1978 ◽  
Vol 33 (9) ◽  
pp. 987-989 ◽  
Author(s):  
J. K. Kouinis ◽  
J. M. Tsangaris ◽  
A. G. Galinos

The preparation of complexes of oxamic acid with Al(III), Ga(III), In(III), Tl(III), Y(III), Fe(III), Mn(II) and V(III) is reported. From the study of the infrared and diffuse reflectance spectra and the magnetic moments (for the complexes of Fe(III), Mn(II) and V(III)) it is concluded that in all complexes the metal ion is coordinated with the carboxyl oxygen and the amidic nitrogen, after the ionization of one of the amidic hydrogens.Octahedral structures are proposed for all the complexes of the trivalent metal ions and the complex K2{Mn(oxamic)2} · 2 H2O.


1977 ◽  
Vol 32 (6) ◽  
pp. 645-647 ◽  
Author(s):  
A. G. Galinos ◽  
J. M. Tsangaris ◽  
J. K. Kouinis

The preparation of the complexes of oxamic acid with Cu(II), Ni(II), Co(II) and Cr(III) is reported. From the study of IR, diffuse reflectance spectra and the magnetic moments it is concluded that in all complexes the metal is coordinated with the amidic nitrogen, after ionization of one amidic hydrogen, and with the carboxyl oxygen.Octahedral structures are proposed for the complexes K2[Ni(oxamic)2] · 2 H2O and K3[Cr(oxamic)3] and planar configurations for K2[Cu(oxamic)2] and K2[Co(oxamic)2].


1974 ◽  
Vol 29 (7-8) ◽  
pp. 538-541 ◽  
Author(s):  
J. M. Tsangaris ◽  
S. M. Paraskewas

The synthesis, IR spectra and UV-visible diffuse reflectance spectra of the complexes [Cu(abeda)]Cl2 and [Ni(abeda)]Cl£, where abeda = N,N′-bis(o-aminobenzyl)ethylenediamine, as well as the magnetic moments of the complexes in the solid state are reported and discussed.


1987 ◽  
Vol 65 (2) ◽  
pp. 409-411 ◽  
Author(s):  
Madanmohan S. Gill ◽  
Anil K. Sethi ◽  
Rajendra D. Verma

U(SO3CF3)4 and MIIUIV(SO3CF3)6, M = Mg, Mn, Fe, Zn, have been prepared by the reaction of their respective trifluoroacetates with HSO3CF3 acid in CF3COOH medium at room temperature. Infrared data indicate bidentate bridging —SO3CF3 groups in these compounds. Magnetic moments show the presence of uranium(IV) species. Diffuse reflectance spectra suggest six coordinate uranium(IV) although the presence of possible eight or higher coordinate uranium(IV) cannot be ruled out. X-ray diffraction studies reveal them to be definite entities.


1981 ◽  
Vol 36 (6) ◽  
pp. 697-703 ◽  
Author(s):  
S. P. Perlepes ◽  
Th. F. Zafiropoulos ◽  
J. K. Kouinis ◽  
A. G. Galinos

Abstract The preparation, for the first time, of the deprotonated complexes of oxamic acid with Ce(III), Pr(III), Nd(III), Sm(III), Eu(III), Dy(III), Ho(III) and Yb(III) is reported. Properties, analytical results, conductometric measurements, magnetic moments and spectral data (IR and diffuse reflectance spectra) are discussed in terms of possible structural types and the nature of the bonding. Oxamic acid acts as a bidentate non-bridging ligand.


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