Prathapachandra Kurup, M R; Sheeja, S R; Sarika, Sivakumar; Neema, Ani Mangalam; Edward, R T Tiekink(Elsevier, June 23, 2009)
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Abstract:
Four hydrazone ligands: 2-benzoylpyridine benzoyl hydrazone (HBPB), di-2-pyridyl ketone nicotinoyl
hydrazone (HDKN), quinoline-2-carbaldehyde benzoyl hydrazone (HQCB), and quinoline-2-carbaldehyde
nicotinoyl hydrazone (HQCN) and four of their complexes with vanadyl salts have been synthesized and
characterized. Single crystals of HBPB and complexes [VO(BPB)(l2-O)]2 (1) and [VO(DKN)(l2-O)]2 ½H2O
(2) were isolated and characterized by X-ray crystallography. Each of the complexes exhibits a binuclear
structure where two vanadium(V) atoms are bridged by two oxygen atoms to form distorted octahedral
structures within cis-N2O4 donor sets. In most complexes, the uninegative anions function as tridentate
ligands, coordinating through the pyridyl- and azomethine-nitrogen atoms and enolic oxygen whereas in
complex [VO(HQCN)(SO4)]SO4 4H2O (4) the ligand is coordinated in the keto form. Complexes [VO(QCB)(
OMe)] 1.5H2O (3) and 4 are found to be EPR active and showed well-resolved axial anisotropy with
two sets of eight line pattern
Prathapachandra Kurup, M R; Reena, T A(Elsevier, March 15, 2010)
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Abstract:
Five copper(II) complexes [CuLCl]2·CuCl2·4H2O (1), [CuLOAc] (2), [CuLNO3]2 (3), [CuLN3] (4) and
[CuLNCS]·3/2H2O (5) of di-2-pyridyl ketone-N4-phenyl-3-semicarbazone (HL) were synthesized and
characterized by elemental analyses and electronic, infrared and EPR spectral techniques. In all these
complexes the semicarbazone undergoes deprotonation and coordinates through enolate oxygen, azomethine
and pyridyl nitrogen atoms. All the complexes are EPR active due to the presence of an unpaired
electron. EPR spectra of all the complexes in DMF at 77K suggest axial symmetry and the presence of
half field signals for the complexes 1 and 3 indicates dimeric structures
Description:
Spectrochimica Acta Part A 76 (2010) 322–327 doi:10.1016/j.saa.2010.03.011
Prathapachandra Kurup, M R; Alex, Punnoose; Manoj, E(Elsevier, October 17, 2008)
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Abstract:
Ten new copper(II) complexes of five potential bisthiocarbohydrazone and biscarbohydrazone ligands
were synthesized and physico-chemically characterized. The spectral and magnetic studies of compounds
are consistent with the formation of asymmetric di-, tri- or tetranuclear copper(II) complexes of deprotonated
forms of respective ligands. The variable temperature magnetic susceptibility measurements of all
complexes showantiferromagnetic interactions between the Cu(II) centers, in agreement with very broad
powder EPR spectra. However, frozen solution EPR spectral studies are found in contradiction with the
solid-state magnetic studies and indicate that the complexes are not very stable in solutions; the possible
fragmentations of complexes are found in agreement with MALDI MS results. The EPR spectral simulation
of most of the compounds is in agreement with the presence of two uncoupled Cu(II) species in solution.
Prathapachandra Kurup, M R; Sreesha, Sasi; Sithambaresan, M; Fun, H K(Elsevier, 2010)
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Abstract:
Four manganese(II) complexes Mn2(paa)2(N3)4 (1), [Mn(paa)2(NCS)2] 3/2H2O (2), Mn(papea)2(NCS)2 (3),
[Mn(dpka)2(NCS)2] 1/2H2O(4) of three neutral N,N donor bidentate Schiff bases were synthesized and physico-
chemically characterized by means of partial elemental analyses, electronic, infrared and EPR spectral
studies. Compounds 3 and 4 were obtained as single crystals suitable for X-ray diffraction. Compound 4
recrystallized as Mn(dpka)2(NCS)2. Both the compounds crystallized in the monoclinic space groups P21
for 3 and C2/c for 4. Manganese(II) is found to be in a distorted octahedral geometry in both the monomeric
complexes with thiocyanate anion as a terminal ligand coordinating through the nitrogen atom. EPR spectra
in DMF solutions at 77 K show hyperfine sextets with low intensity forbidden lines lying between each
of the two main hyperfine lines and the zero field splitting parameters (D and E) were calculated.