Evidence from infrared spectra for the magnetic moment directions of CR cations in the spinel ferrites

2015 ◽  
Vol 463 ◽  
pp. 26-29 ◽  
Author(s):  
G.D. Tang ◽  
Z.F. Shang ◽  
X.Y. Zhang ◽  
J. Xu ◽  
Z.Z. Li ◽  
...  
1969 ◽  
Vol 22 (8) ◽  
pp. 1613 ◽  
Author(s):  
PSK Chia ◽  
SE Livinhstone

Mono-ligand complexes of 6-methylpyrid-2-yl-N-(2?-methylthiophenyl)- methyleneimine (SNSMe) of the type MX2(SNNMe) (M = Mn, Fe, Co, Xi, and Cu; X = Cl, Br, I, or NCS) have been prepared. Infrared data show that in all the complexes the ligand (SNNMe) is tridentate. The electronic and infrared spectra indicate that the complexes of manganese, iron, and cobalt are five-coordinate, whereas the nickel and copper complexes are six-coordinate and polymeric. The complex CO(NO3)2(SNNMe) is six- coordinate and contains one bidentate and one unidentate nitrato group. ��� The bis-ligand complexes [N(SNNMe)2]Y2 (M = Fe, Ni, and Cu; Y = ClO4 or BF4) were also isolated. The iron complex is low-spin (μ 1.5 B.M.) but the magnetic moment of the nickel complex (μ 3.0 B.M.) is normal for high-spin octahedral nickel(II).


2021 ◽  
Vol 33 (9) ◽  
pp. 2207-2211
Author(s):  
Usha Bansal ◽  
Samta Goyal ◽  
Swati Agrawal

Manganese(II) and cobalt(II) complexes were synthesized with [N4] tetradentate macrocyclic ligand using different metal salts i.e. MnCl2, Mn(NO3)2, CoCl2 and Co(NCS)2. The ligand was prepared by condensation of glyoxal and carbahydrazide. All these were characterized by elemental analysis, molar conductance measurements, magnetic moment, IR, mass, electronic and EPR spectral studies. Elemental analysis indicates that the complexes have composition MLX2 where (X = Cl–, NO3 –,NCS–). All the complexes were found to be non-electrolytic in nature so can be formulated as [MLX2]. Infrared spectra of metal complexes suggest that the ligand behaves as tetradentate. On the basis of magnetic moment, electronic and EPR spectral data, all the metal complexes were found to be high spin with octahedral geometry.


AIP Advances ◽  
2015 ◽  
Vol 5 (9) ◽  
pp. 097167 ◽  
Author(s):  
L. C. Xue ◽  
L. L. Lang ◽  
J. Xu ◽  
Z. Z. Li ◽  
W. H. Qi ◽  
...  

2015 ◽  
Vol 64 (1) ◽  
pp. 017501
Author(s):  
Xu Jing ◽  
Qi Wei-Hua ◽  
Ji Deng-Hui ◽  
Li Zhuang-Zhi ◽  
Tang Gui-De ◽  
...  

1974 ◽  
Vol 52 (21) ◽  
pp. 3607-3611 ◽  
Author(s):  
G. Marcotrigiano ◽  
G. C. Pellacani

Compounds of the type [CuA2•H2O]2 and [CuA2•4H2O]2 have been prepared, where A is N-acetylglycine (aceturic acid). Amine adducts of the type CuA2B (B = piperazine, 2,2′-bipyridine, and 1,10-phenantroline) and CuA2B2 (B = N-methylpiperazine, piperidine, morpholine, pyridine, and ethylenediamine) were obtained by reaction of the amines with CuA2•4H2O. Each complex was characterized by elemental analysis, infrared spectrum, electronic spectrum, and magnetic moment. For the piperazine and ethylenediamine adducts a square-planar pattern of coordination about copper(II) ion is probable, while for the other amine adducts a square-pyramidal structure is proposed. For all the complexes the coordination of the N-acetylglycine occurs only through the terminal carboxyl oxygen in a monodentate arrangement.


1974 ◽  
Vol 29 (7-8) ◽  
pp. 492-494 ◽  
Author(s):  
A. Syamal

A reinvestigation of the title compound is reported. The compound has been prepared by a modified method and characterised by infrared spectra, electronic spectra and magnetic susceptibility measurements. The infrared spectral data suggest that the two coordinated thiocyanate ions are bonded to chromium(III) through N atoms rather than the S atoms. The complex exhibits two ligand field bands at 20410 and 26660 cm-1 due to the transitions 4A2g → 4T2g and 4A2g → 4T1g (F) respectively. Electronic spectral and magnetic moment data suggest that the complex has an octahedral structure with d2sp3 bonding.


1981 ◽  
Vol 78 ◽  
pp. 927-932 ◽  
Author(s):  
F.J.C.M. Toolenaar ◽  
G.J. van der Poort ◽  
F. Stoop ◽  
V. Ponec

Author(s):  
Daniel Tabor ◽  
Timothy Zwier ◽  
Joseph Korn ◽  
Daniel Hewett ◽  
Edwin Sibert
Keyword(s):  

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