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Slow Magnetic Relaxation And Electron Delocalization In An S = 9/2 Iron(Ii/Iii) Complex With Two Crystallographically Inequivalent Iron Sites, Susanta Hazra, Sujit Sasmal, Michel Fleck, Fernande Grandjean, Moulay T. Sougrati, Meenakshi Ghosh, T. David Harris, Pierre Bonville, Gary J. Long, Sasankasekhar Mohanta
Slow Magnetic Relaxation And Electron Delocalization In An S = 9/2 Iron(Ii/Iii) Complex With Two Crystallographically Inequivalent Iron Sites, Susanta Hazra, Sujit Sasmal, Michel Fleck, Fernande Grandjean, Moulay T. Sougrati, Meenakshi Ghosh, T. David Harris, Pierre Bonville, Gary J. Long, Sasankasekhar Mohanta
Chemistry Faculty Research & Creative Works
The magnetic, electronic, and Mössbauer spectral properties of Fe 2L(µ-OAc)2ClO4, 1, where L is the dianion of the tetraimino-diphenolate macrocyclic ligand, H2L, indicate that 1 is a class III mixed valence iron(II/III) complex with an electron that is fully delocalized between two crystallographically inequivalent iron sites to yield a [Fe2]V cationic configuration with a St 9/2 ground state. Fits of the dc magnetic susceptibility between 2 and 300K and of the isofield variable-temperature magnetization of 1 yield an isotropic magnetic exchange parameter, J, of -32(2) cm-1 for an …
Polarized Neutron Diffraction And Mössbauer Spectral Study Of Short-Range Magnetic Correlations In The Ferrimagnetic Layered Compounds (Pph₄) [FeIiFeIii(Ox)₃] And (Nbu₄) [FeIiFeIii(Ox)₃], Simon G. Carling, Dirk W. Visser, Dimitri Hautot, Ian D. Watts, Peter Day, Jürgen Ensling, Phillip Gütlich, Gary J. Long, Fernande Grandjean
Polarized Neutron Diffraction And Mössbauer Spectral Study Of Short-Range Magnetic Correlations In The Ferrimagnetic Layered Compounds (Pph₄) [FeIiFeIii(Ox)₃] And (Nbu₄) [FeIiFeIii(Ox)₃], Simon G. Carling, Dirk W. Visser, Dimitri Hautot, Ian D. Watts, Peter Day, Jürgen Ensling, Phillip Gütlich, Gary J. Long, Fernande Grandjean
Chemistry Faculty Research & Creative Works
Short-range antiferromagnetic correlations have been studied in the layered compounds (PPh4) [FeIIFeIII(ox)3] and (NBu4) [FeIIFeIII(ox)3] by neutron polarization analysis and Mössbauer spectroscopy. Polarized neutron diffraction profiles obtained between 2 and 50 K on (d20-Pph4) [FeIIFeIII(ox)3] show no magnetic Bragg scattering; the lack of such scattering indicates the absence of long-range magnetic order. However, a broad asymmetric feature observed at a Q of ca. 0.8 Å-1 is attributed to two-dimensional short-range magnetic correlations, which …
A Mössbauer Spectral Study Of The Magnetic Properties Of Ho₂Fe₁₇ And Ho₂Fe₁₇D₃.₈, Gary J. Long, Olivier Isnard, Fernande Grandjean
A Mössbauer Spectral Study Of The Magnetic Properties Of Ho₂Fe₁₇ And Ho₂Fe₁₇D₃.₈, Gary J. Long, Olivier Isnard, Fernande Grandjean
Chemistry Faculty Research & Creative Works
The Mössbauer spectra of Ho2Fe17 and Ho2Fe17D3.8 have been measured between 4.2 and 295 K and analyzed with a model which takes into account both the disordered nonstoichiometric hexagonal Th2Ni17-like structure and the basal orientation of the iron magnetic moments. The isomer shifts of the five crystallographically inequivalent iron sites in both Ho2Fe17 and Ho2Fe17D3.8 follow the sequence of Wigner-Seitz cell volumes and their temperature dependence follows the typical second-order Doppler shift. An increase in the weighted average isomer shift …
Magnetic And Mössbauer Spectral Evidence For The Suppression Of The Magnetic Spin Reorientation In Tm₂Fe₁₇ By Deuterium, Fernande Grandjean, Olivier Isnard, Gary J. Long
Magnetic And Mössbauer Spectral Evidence For The Suppression Of The Magnetic Spin Reorientation In Tm₂Fe₁₇ By Deuterium, Fernande Grandjean, Olivier Isnard, Gary J. Long
Chemistry Faculty Research & Creative Works
The structural and magnetic properties of Tm2Fe17 and Tm2Fe17D3.2 are investigated by means of x-ray-diffraction, thermal, and ac magnetic susceptibility measurements, and iron-57 Mössbauer spectroscopy. Both compounds crystallize in a hexagonal P63/mmc space group with a Th2Ni17-like structure. Deuterium insertion into Tm2Fe17 induces large increases in the unit-cell volume, the saturation magnetization, and the ordering temperature. The unit-cell expansion is anisotropic, with a larger increase in the a lattice parameter than the c lattice parameter. A spin reorientation is observed at 90 K …
Mössbauer Spectral Study Of The Magnetic Properties Of Ce₂Fe₁₇Hₓ (X=0, 1, 2, 3, 4, And 5), Dimitri Hautot, Gary J. Long, Fernande Grandjean, Olivier Isnard
Mössbauer Spectral Study Of The Magnetic Properties Of Ce₂Fe₁₇Hₓ (X=0, 1, 2, 3, 4, And 5), Dimitri Hautot, Gary J. Long, Fernande Grandjean, Olivier Isnard
Chemistry Faculty Research & Creative Works
The Mössbauer spectra of Ce2Fe17Hx, where x=0, 1, 2, 3, 4, and 5, have been measured and analyzed between 4.2 and 295 K. Because Ce2Fe17 exhibits a helical magnetic order between 225 and 90 K and a fan magnetic order below 90 K, its Mössbauer spectra were fit with a distribution of hyperfine fields and θ angles for four of the eight magnetically inequivalent sites. Because the hydrides exhibit a magnetization within the basal plane of the hexagonal cell, their Mössbauer spectra were fit with seven sextets. The four isomer shifts …
Reply To "Comment On 'Mössbauer Effect Study Of Filled Antimonide Skutterudites'", Gary J. Long, Gary J. Long, Dimitri Hautot, Fernande Grandjean, Donald T. Morelli, Gregory P. Meisner
Reply To "Comment On 'Mössbauer Effect Study Of Filled Antimonide Skutterudites'", Gary J. Long, Gary J. Long, Dimitri Hautot, Fernande Grandjean, Donald T. Morelli, Gregory P. Meisner
Chemistry Faculty Research & Creative Works
The temperature dependence of the isomer shift of α-iron between 4.2 and 990 K and of Dy3Fe5O12 between 4.2 and 550 K has been analyzed in terms of the Debye model for the second-order Doppler shift, a model in which an additional parameter, the effective vibrating mass, is included. This mass is found equal to 57 g/mol in the ionic compound, Dy3Fe5O12, and equal to 60 g/mol in metallic α-iron. The deviation of this mass from 57 g/mol is a measure of the covalency of the metallic bonding in …