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S A Zvyagin

Publications and source records attributed to S A Zvyagin.

11 recordsLinked to original sources
PubMed2006

Electronic structure of four-coordinate C3v nickel(II) scorpionate complexes: investigation by high-frequency and -field electron paramagnetic resonance and electronic absorption spectroscopies.

A series of complexes of formula TpNiX, where Tp*- = hydrotris(3,5-dimethylpyrazole)borate and X = Cl, Br, I, has been characterized by electronic absorption spectroscopy in the visible and near-infrared (NIR) region and by high-frequency and -field electron paramagnetic resonance (HFEPR) spectroscopy. The crystal structure of TpNiCl has been previously reported; that for TpNiBr is given here: space group = Pmc2(1), a = 13.209(2) A, b = 8.082(2) A, c = 17.639(4) A, alpha = beta = gamma = 90 degrees , Z = 4. TpNiX contains a four-coordinate nickel(II) ion (3d8) with approximate C3v point group symmetry about the metal and a resulting S = 1 high-spin ground state. As a consequence of sizable zero-field splitting (zfs), TpNiX complexes are "EPR silent" with use of conventional EPR; however, HFEPR allows observation of multiple transitions. Analysis of the resonance field versus the frequency dependence of these transitions allows extraction of the full set of spin Hamiltonian parameters. The axial zfs parameter for TpNiX displays pronounced halogen contributions down the series: D = +3.93(2), -11.43(3), -22.81(1) cm(-1), for X = Cl, Br, I, respectively. The magnitude and change in sign of D observed for TpNiX reflects the increasing bromine and iodine spin-orbit contributions facilitated by strong covalent interactions with nickel(II). These spin Hamiltonian parameters are combined with estimates of 3d energy levels based on the visible-NIR spectra to yield ligand-field parameters for these complexes following the angular overlap model (AOM). This description of electronic structure and bonding in a pseudotetrahedral nickel(II) complex can enhance the understanding of similar sites in metalloproteins, both native nickel enzymes and nickel-substituted zinc enzymes.

Journal Article↗
PubMed2005

Tunable-frequency high-field electron paramagnetic resonance.

A tunable-frequency methodology based on backward wave oscillator sources in high-frequency and -field EPR (HFEPR) is described. This methodology is illustrated by an application to three non-Kramers transition metal ion complexes and one Kramers ion complex. The complexes are of: Ni(II) (S=1) as found in dichlorobistriphenylphosphanenickel(II), Mn(III) (S=2) as found in mesotetrasulfonatoporphyrinatomanganese(III) chloride, Fe(II) (S=2) as found in ferrous sulfate tetrahydrate, and Co(II) (S=3/2) as found in azido(tris(3-tert-butylpyrazol-1-yl)hydroborate)cobalt(II). The above Ni(II) and Mn(III) complexes have been studied before by HFEPR using the multifrequency methodology based on Gunn oscillator sources, but not by the present method, while the Fe(II) and Co(II) complexes presented here have not been studied by any form of HFEPR. Highly accurate spin Hamiltonian parameters can be obtained by the experimental methodology described here, in combination with automated fitting procedures. This method is particularly successful in determining g-matrix parameters, which are very difficult to extract for high-spin systems from single frequency (or a very limited set of multi-frequency) HFEPR spectra, but is also able to deliver equally accurate values of the zero-field splitting tensor. The experimental methods involve either conventional magnetic field modulation or an optical modulation of the sub-THz wave beam. The relative merits of these and other experimental methods are discussed.

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PubMed2005

Electron spin resonance in sine-gordon spin chains in the perturbative spinon regime.

We report the low-temperature multifrequency ESR studies of copper pyrimidine dinitrate, a spin-1/2 antiferromagnetic chain with alternating g tensor and the Dzyaloshinskii-Moriya interaction, allowing us to test a new theoretical concept proposed recently by Oshikawa and Affleck [Phys. Rev. Lett. 82, 5136 (1999)]. Their theory, based on bosonization and self-energy formalism, can be applied for precise calculation of ESR parameters of S=1/2 antiferromagnetic chains in the perturbative spinon regime. Excellent quantitative agreement between the theoretical predictions and experiment is obtained.

Journal Article↗
PubMed2005

Synthesis, characterization, and physicochemical properties of manganese(III) and manganese(V)-oxo corrolazines.

The structural and physicochemical properties of the manganese-corrolazine (Cz) complexes (TBP8Cz)Mn(V)O (1) and (TBP8Cz)Mn(III) (2) (TBP = p-tert-butylphenyl) have been determined. Recrystallization of 2 from toluene/MeOH resulted in the crystal structure of (TBP8Cz)Mn(III)(CH3OH) (2 x MeOH). The packing diagram of 2 x MeOH reveals hydrogen bonds between MeOH axial ligands and meso N atoms of adjacent molecules. Solution binding studies of 2 with different axial ligands (Cl-, Et3PO, and Ph3PO) reveal strong binding, corroborating the preference of the Mn(III) ion for a five-coordinate environment. High-frequency and field electron paramagnetic resonance (HFEPR) spectroscopy of solid 2 x MeOH shows that 2 x MeOH is best described as a high-spin (S = 2) Mn(III) complex with zero-field splitting parameters typical of corroles. Structural information on 1 was obtained through an X-ray absorption near-edge structure (XANES)/extended X-ray absorption fine structure (EXAFS) study and compared to XANES/EXAFS data for 2 x MeOH. The XANES data for 1 shows an intense pre-edge transition characteristic of a high-valent metal-oxo species, and a best fit of the EXAFS data gives a short Mn-O bond distance of 1.56 A, confirming the structure of the metal-oxo unit in 1. Detailed spectroelectrochemical studies of 1 and 2 were performed revealing multiple reversible redox processes for both complexes, including a relatively low potential for the Mn(V) --> Mn(IV) process in 1 (near 0.0 V vs saturated calomel reference electrode). Chemical reduction of 1 results in the formation of a Mn(III)Mn(IV)(mu-O) dimer as characterized by electron paramagnetic resonance spectroscopy.

Binding Sites↗
PubMed2005

High-frequency/high-field EPR spectroscopy of the high-spin ferrous ion in hexaaqua complexes.

Electron paramagnetic resonance (EPR) at conventional magnetic fields and microwave frequencies, respectively, B0 < or = 1.5 T, nu < or = 35 GHz, has been widely applied to odd electron-number (S = 1/2) transition metal complexes. This technique is less successfully applied to high-spin systems that have even electron configurations, e.g. Fe2+ (S = 2). The recently developed technique of high-frequency and high-field EPR (HFEPR), employing swept fields up to 25 T combined with multiple, sub-THz frequencies readily allows observation of EPR transitions in such high-spin systems. A parallel spectroscopic technique is frequency-domain magnetic resonance spectroscopy (FDMRS), in which the frequency is swept while at zero, or at discrete applied magnetic fields. We describe here the application of HFEPR and FDMRS to two simple high-spin (HS) ferrous (Fe2+) salts: ferrous perchlorate hydrate, [Fe(H2O)6](ClO4)2 and (NH4)2[Fe(H2O)6](SO4)2, historically known as ferrous ammonium sulfate. Both compounds contain hexaaquairon(II). The resulting spectra were analyzed using a spin Hamiltonian for S = 2 to yield highly accurate spin-Hamiltonian parameters. The complexes were also studied by powder DC magnetic susceptibility and zero-field Mössbauer effect spectroscopy for corroboration of magnetic resonance results. In the case of [Fe(H2O)6](ClO4)2, all the magnetic techniques were in excellent agreement and gave as consensus values: D = 11.2(2) cm(-1), E = 0.70(1) cm(-1). For (NH4)2[Fe(H2O)6](SO4)2, FDMRS and HFEPR gave D = 14.94(2) cm(-1), E = 3.778(2) cm(-1). We conclude that the spin-Hamiltonian parameters for the perchlorate best represent those for the isolated hexaaquairon(II) complex. To have established electronic parameters for the fundamentally important [Fe(H2O)6]2+ ion will be of use for future studies on biologically relevant systems containing high-spin Fe2+.

Journal Article↗
PubMed2004

Pseudooctahedral complexes of vanadium(III): electronic structure investigation by magnetic and electronic spectroscopy.

A variety of physical methods has been used to probe the non-Kramers, S = 1, V(III) ion in two types of pseudooctahedral complexes: V(acac)(3), where acac = anion of 2,4-pentanedione, and VX(3)(thf)(3), where thf = tetrahydrofuran and X = Cl and Br. These methods include tunable frequency and high-field electron paramagnetic resonance (HFEPR) spectroscopy (using frequencies of approximately 95-700 GHz and fields up to 25 T) in conjunction with electronic absorption, magnetic circular dichroism (MCD), and variable-temperature variable-field MCD (VTVH-MCD) spectroscopies. Variable-temperature magnetic susceptibility and field-dependent magnetization measurements were also performed. All measurements were conducted on complexes in the solid state (powder or mull samples). The field versus sub-THz wave quantum energy dependence of observed HFEPR resonances yielded the following spin Hamiltonian parameters for V(acac)(3): D = +7.470(1) cm(-1); E = +1.916(1) cm(-1); g(x) = 1.833(4); g(y) = 1.72(2); g(z) = 2.03(2). For VCl(3)(thf)(3), HFEPR detected a single zero-field transition at 15.8 cm(-1) (474 GHz), which was insufficient to determine the complete set of spin Hamiltonian parameters. For VBr(3)(thf)(3), however, a particularly rich data set was obtained using tunable-frequency HFEPR, and analysis of this data set gave the folowing: D = -16.162(6) cm(-1); E = -3.694(4) cm(-1); g(x) = 1.86(1); g(y) = 1.90(1); g(z) = 1.710(4). Analysis of the VTVH-MCD data gave spin Hamiltonian parameters in good agreement with those determined by HFEPR for both V(acac)(3) and VBr(3)(thf)(3) and in rough agreement with the estimate for VCl(3)(thf)(3) (D approximately 10 cm(-1), |E/D| approximately 0.18), together with the finding that the value of D is negative for both thf complexes. The electronic structures of these V(III) complexes are discussed in terms of their molecular structures and the electronic transitions observed by electronic absorption and MCD spectroscopies.

Journal Article↗
PubMed2004

Magnetic-field-induced condensation of triplons in Han Purple pigment BaCuSi2O6.

Besides being an ancient pigment, BaCuSi2O6 is a quasi-2D magnetic insulator with a gapped spin dimer ground state. The application of strong magnetic fields closes this gap, creating a gas of bosonic spin triplet excitations. The topology of the spin lattice makes BaCuSi2O6 an ideal candidate for studying the Bose-Einstein condensation of triplet excitations as a function of the external magnetic field, which acts as a chemical potential. In agreement with quantum Monte Carlo numerical simulations, we observe a distinct lambda anomaly in the specific heat together with a maximum in the magnetic susceptibility upon cooling down to liquid helium temperatures.

Journal Article↗
PubMed2004

Excitation hierarchy of the quantum sine-gordon spin chain in a strong magnetic field.

The magnetic excitation spectrum of copper pyrimidine dinitrate, a material containing S = 1 / 2 antiferromagnetic chains with alternating g tensor and the Dzyaloshinskii-Moriya interaction and exhibiting a field-induced spin gap, is probed using submillimeter wave electron spin resonance spectroscopy. Ten excitation modes are resolved in the low-temperature spectrum, and their frequency-field diagram is systematically studied in magnetic fields up to 25 T. The experimental data are sufficiently detailed to make a very accurate comparison with predictions based on the quantum sine-Gordon field theory. Signatures of three breather branches and a soliton, as well as those of several multiparticle excitation modes, are identified.

Journal Article↗
PubMed2004

High-frequency and -field EPR of a pseudo-octahedral complex of high-spin Fe(II): bis(2,2'-bi-2-thiazoline)bis(isothiocyanato)iron(II).

A pseudo-octahedral complex of high-spin Fe(II), bis(2,2'-bi-2-thiazoline)bis(isothiocyanato)iron(II), which has a cis-FeN'2N4 chromophore, has been investigated by high-frequency, high-field electron paramagnetic resonance (HFEPR). Complementary Mössbauer and DC magnetic susceptibility studies were also performed. HFEPR spectra of powder samples were recorded at frequencies up to 700 GHz and over a magnetic field range of 0-25 T. Analysis of the field-frequency data set yields the following set of spin Hamiltonian parameters for S = 2: D = +12.427(12) cm-1, E = +0.243(3) cm-1; gx = 2.147(3), gy = 2.166(3), gz = 2.01(1). The parameters are analyzed by use of a simple crystal-field model. This study represents the first precise determination by HFEPR of spin Hamiltonian parameters in six-coordinate high-spin Fe(II) and indicates the applicability of HFEPR to the study of high-spin Fe(II) in coordination complexes and biological model compounds.

Computer Simulation↗
PubMed2004

Definitive spectroscopic determination of zero-field splitting in high-spin cobalt(II).

A high-spin Co(II) complex (3d(7), S = 3/2), Co(PPh(3))(2)Cl(2) (Ph = phenyl), has been investigated in the solid state by both high-frequency and -field electron paramagnetic resonance (HFEPR) and by variable-temperature, variable-field magnetic circular dichroism (VTVH-MCD). In HFEPR spectroscopy, the combination of variable sub-THz frequencies generated by backward wave oscillators (150-700 GHz, corresponding to energy 5-23 cm(-1)) and high magnetic fields (0-25 T) constitutes a novel experimental technique allowing accurate determination of a complete set of spin Hamiltonian parameters for this complex: D = -14.76(2) cm(-1), E = 1.141(8) cm(-1), g(x) = 2.166(4), g(y) = 2.170(4), g(z) = 2.240(5). Independent VTVH-MCD studies on multiple absorption bands of the complex yield D = -14(3) cm(-1), E = 0.96(20) cm(-1) (absolute value of E/D = 0.08(2)), g(x) = 2.15(5), g(y) = 2.16(4), and g(z) = 2.17(3). This very good agreement between HFEPR and MCD indicates that there is no inherent discrepancy between these two quite different experimental techniques. Thus, depending on the nature of the sample, either can be reliably used to determine zero-field splitting parameters in high-spin Co(II), with the HFEPR being more accurate but VTVH-MCD being more sensitive.

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