NUKLEONIKA 2004, 49(Supplement 3):s13-s16
Tomasz Kaczmarzyk1, Tomasz Jackowski1, Kazimierz Dziliński1, Gennadij N. Sinyukov2
1 Institute of Physics, Technical University of Częstochowa, 19 Armii Krajowej Ave., 42-200 Częstochowa, Poland,
2 Institute of Molecular and Atomic Physics, Belarus Academy of Sciences, 20 F. Skoryny Prosp., 220 072 Minsk, Belarus
Electron configuration changes of Fe(III) ions in porphyrin complexes with chloride axial ligands caused
by the successive nitrogen substitution of CH methine bridges at meso positions of the porphyrin
ring is discussed on the basis of Mössbauer spectroscopy results. It was shown that increase of a
number of nitrogen atoms at the meso positions changes the character of quantum-mechanically
mixed spin state of Fe(III) ions (S = 5/2 + 3/2) by the increase of the intermediate-spin
(S = 3/2) contribution. This feature is reflected in Mössbauer spectra by an increase of
quadrupole splitting values and the decrease of the asymmetry of quadrupole doublets, when the number
of nitrogen atoms at the meso positions increases. Isomer shifts remain practically unchanged. These
peculiarities are discussed in the light of spin relaxation mechanisms and the occupancy of d
orbitals in Fe(III) ions coordinated to the porphyrin ring and chloride ligand. It has been noticed that
Mössbauer parameters correlate qualitatively with EPR data.