Low-spin State Research Articles

Nuclear Structure and Decay Data for A = 222 Isobars

Evaluated data are presented for 11 known A=222 nuclides (Bi, Po, At, Rn, Fr, Ra, Ac, Th, Pa, U, and Np), and relevant Jπ and T1/2 data for A=226 nuclei decaying by α-decay to A=222 nuclei. For 222Bi, only the isotopic identification is established with no measurement of its half-life. For 222Po, 222At, 222Fr, 222U, and 222Np, data are available only for the ground states, with static magnetic dipole and electric quadrupole moments, and charge radius measurements for the 222Fr ground state. For 222Ac and 222Pa, two low-lying levels are known from 226Pa α decay, and 226Np decay, respectively, but with no information about Jπ assignments and γ decays of these levels. For 222Pa, a long-lived isomeric state is known, decaying dominantly by α decay. 222Rn, 222Ra, and 222Th have been investigated in detail, the low-spin states by α decay and the high-spin studies of ground-state and octupole bands by in-beam γ-ray studies for all the three nuclei, as well as by Coulomb excitation for 222Rn and 222Ra. Low-spin levels in 222Ra have been investigated also through the β− decay of 222Fr. Half-lives of the excited states are known for 7 levels in 222Rn, 12 levels in 222Ra, and 3 levels in 222Th. Octupole deformations, with the presence of alternating-parity bands up to (16+) and (21−) in 222Rn, (20+) and (19−) in 222Ra, and (26+) and (25−) in 222Th, and with interband E1 transitions, have been established in these three nuclei. The present evaluation supersedes the previous A=222 ENSDF evaluations: (2011Si24), (1996El01), (1987El06) and (1977To14).

Engineering High-Spin State Cobalt Cations in Sulfide Spinel for Enhancing Water Oxidation.

The spin states of active sites have a significant impact on the adsorption/desorption ability of the reaction intermediates during the oxygen evolution reaction (OER). Sulfide spinel is not generally considered a highly efficient OER catalyst owing to the low spin state of Co3+ and the lack of unpaired electrons available for adsorption of reaction intermediates. Herein, it is proposed a novel Nd-evoked valence electronic adjustment strategy to engineer the spin state of Co ions. The unique f-p-d orbital electronic coupling effect stimulates the rearrangement of Co d orbital electrons and increases the eg electron filling to achieve high-spin state Co ions, which promotes charge transport by propagating a spin channel and generates a high number of active sites for intermediate adsorption. The optimized CuCo1.75 Nd0.25 S4 catalyst exhibits outstanding electrocatalytic properties with a low overpotential of 320mV at 500mAcm-2 and a 48h stability at 300mAcm-2 . In situ synchrotron radiation infrared spectra confirm the quick accumulation of key *OOH and *O intermediates. This work deepens the comprehensive understanding of the relationship between OER activity and spin configurations of Co ions and offers a new design strategy for spinel compound catalysts.

Nagaoka ferromagnetism in an array of phosphorene quantum dots.

We consider an array of four quantum dots defined in phosphorene containing three excess electrons, i.e., in the conditions of near half filling when itinerant Nagaoka ferromagnetism is expected to appear in a square array with isotropic interdot hopping. The interdot hopping in the array arranged in a square inherits the anisotropy from the form of the phosphorene conduction band. We apply the configuration interaction method for discussion of the appearance and stability of the spin-polarized ground state and discuss the compensation of the effective mass anisotropy by the geometry of the quantum dot array. Our study shows strong stability of Nagaoka ferromagnetism for optimized geometry of the array, with the Nagaoka gap as large as ∼230µeV. A phase diagram for the ground-state spin ordering versus the geometric parameters of the array is presented. We study the suppression of the ferromagnetism in a transition of the [Formula: see text] array to a quasi-1D chain and indicate that the shift of one of the quantum dots away from the array center is enough to transform the system to a quantum dot chain. A shift in the zigzag crystal direction induces the low-spin ground state more effectively than a shift along the armchair direction. We also discuss the robustness of the spin ordering against detuning one of the dots. The ferromagnetic ground-state survives as long as the detuning is not large enough to trap one of the electrons within a single quantum dot (for positive detuning) or remove one of the quantum dots of the accessible energy range (for negative detuning).

A route to high-accuracy abinitio description of electronic excited states in high-spin lanthanide-containing species: A case study of GdO.

Accurate description of electronic excited states of high-spin molecular species is a yet unsolved problem in modern electronic structure theory. A composite computational scheme developed in the present work contributes to solving this task for a challenging case of lanthanide-containing molecules. In the scheme, the highest-spin states whose wavefunctions are dominated by a single Slater determinant are described at the single-reference (SR) CCSD(T) level, whereas the lower-spin states, being inherently multiconfigurational in their nature, are treated with multireference (MR) methods, MRCI and/or CASPT2. An original technique which scales MR results against SR CCSD(T) ones to improve the accuracy in the former is proposed and examined, taking the example of 12 electronic states of gadolinium monoxide, X9Σ-, Y7Σ-, A'9Δ, A1'7Δ, A9Π, A17Π, B9Σ-, B17Σ-, C9Π, C17Π, D9Σ-, and D17Σ-, up to 35 000cm-1. A multitude of the corresponding Ω (spin-coupled) states was then studied within the state-interacting approach employing the full Breit-Pauli spin-orbit coupling operator with CASSCF-generated ΛS states as a basis. For all ΛS and Ω states, the Gd-O bond lengths, spectroscopic constants ωe, ωexe, αe, and adiabatic excitation energies are obtained. The theoretical predictions are in good agreement with the experimental data, with deviations in excitation energies not exceeding 350cm-1 (1 kcal/mol). The spectroscopic properties of the yet unobserved electronic states, A'9Δ, A1'7Δ, C9Π, C17Π, D9Σ-, and D17Σ-, are evaluated for the first time.

Ultrafast x-ray detection of low-spin iron in molten silicate under deep planetary interior conditions.

The spin state of Fe can alter the key physical properties of silicate melts, affecting the early differentiation and the dynamic stability of the melts in the deep rocky planets. The low-spin state of Fe can increase the affinity of Fe for the melt over the solid phases and the electrical conductivity of melt at high pressures. However, the spin state of Fe has never been measured in dense silicate melts due to experimental challenges. We report detection of dominantly low-spin Fe in dynamically compressed olivine melt at 150 to 256 gigapascals and 3000 to 6000 kelvin using laser-driven shock wave compression combined with femtosecond x-ray diffraction and x-ray emission spectroscopy using an x-ray free electron laser. The observation of dominantly low-spin Fe supports gravitationally stable melt in the deep mantle and generation of a dynamo from the silicate melt portion of rocky planets.

Atomic high-spin cobalt(II) center for highly selective electrochemical CO reduction to CH3OH

In this work, via engineering the conformation of cobalt active center in cobalt phthalocyanine molecular catalyst, the catalytic efficiency of electrochemical carbon monoxide reduction to methanol can be dramatically tuned. Based on a collection of experimental investigations and density functional theory calculations, it reveals that the electron rearrangement of the Co 3d orbitals of cobalt phthalocyanine from the low-spin state (S = 1/2) to the high-spin state (S = 3/2), induced by molecular conformation change, is responsible for the greatly enhanced CO reduction reaction performance. Operando attenuated total reflectance surface-enhanced infrared absorption spectroscopy measurements disclose accelerated hydrogenation of CORR intermediates, and kinetic isotope effect validates expedited proton-feeding rate over cobalt phthalocyanine with high-spin state. Further natural population analysis and density functional theory calculations demonstrate that the high spin Co2+ can enhance the electron backdonation via the dxz/dyz−2π* bond and weaken the C-O bonding in *CO, promoting hydrogenation of CORR intermediates.

On the Jahn-Teller Effect in Silver Complexes of Dimethyl Amino Phenyl Substituted Phthalocyanine.

The structures of Ag complexes with dimethyl amino phenyl substituted phthalocyanine m[dmaphPcAg]q of various charges q and in the two lowest spin states m were optimized using the B3LYP method within the D4h symmetry group and its subgroups. The most stable reaction intermediate in the supposed photoinitiation reaction is 3[dmaphPcAg]-. Group-theoretical analysis of the optimized structures and of their electron states reveals two symmetry-descent mechanisms. The stable structures of maximal symmetry of complexes 1[dmaphPcAg]+, 3[dmaphPcAg]+, 2[dmaphPcAg]0, and 4[dmaphPcAg]2- correspond to the D4 group as a consequence of the pseudo-Jahn-Teller effect within unstable D4h structure. Complexes 4[dmaphPcAg]0, 1[dmaphPcAg]-, 3[dmaphPcAg]-, and 2[dmaphPcAg]2- with double degenerate electron ground states in D4h symmetry structures undergo a symmetry descent to stable structures corresponding to maximal D2 symmetry, not because of a simple Jahn-Teller effect but due to a hidden pseudo-Jahn-Teller effect (strong vibronic interaction between excited electron states). The reduction of the neutral photoinitiator causes symmetry descent to its anionic intermediate because of vibronic interactions that must significantly affect the polymerization reactions.

Modulation of magnetism in transition-metal-doped monolayer MoS2 by strain engineering

It is important to induce and manipulate magnetism in two-dimensional materials for developing low-dimensional spintronic devices. Here we explored the modulation of magnetism in MoS2 monolayers doped with 3d and 4d transition-metal (TM) atoms by strain engineering using first-principles calculations. It is found that 3d TM atom doping tends to induce high spin in TM-MoS2 monolayers, while 4d TM atom doping tends to induce low spin. The magnetic states in TM-MoS2 monolayers can be further mediated by TM-S bond interaction and change of crystal structure symmetry, which is achieved by strain engineering. An increase in the ionic bonding interaction of TM-S modulated by strain leads to an increase of the unpaired electrons accumulated on the TM and S atoms, thus giving rise to the interesting variation in the magnetic moments with strain. Strain is also able to modulate the crystal structures to undergo or not Jahn-Teller (J-T) distortion effects. The structures having J-T distortion will result in low spin states. The research results offer important theoretical support for further application of strain-driven spin devices on MoS2 nanostructures.

Dynamic Aggregation Triggering Reversible Spin-State Switching.

The manipulation of spin-state switching (SSS) under ambient conditions is of significant importance for the construction of molecular switches. Herein, we demonstrate that reversible SSS can be mediated by the aggregation state of a near-infrared (NIR)-sensitive ferrous complex. The ferrous complex was J-aggregated in a DMF suspension and with a low-spin (LS) state; however, with the addition of water, it changed to H-aggregation and reached a high-spin (HS) state, owing to the enhanced intramolecular charge transfer and metal-to-ligand charge transfer. Interestingly, the following NIR irradiation can restore the J-aggregation and LS states owing to the enhanced ligand-to-ligand charge transfer. More interestingly, the ferrous complex can be further incorporated into a hygroscopic sponge that was capable of capturing humidity effectively for all weather conditions, which displayed reversible SSS via alternating atmospheric humidity capture and NIR irradiation under ambient conditions in the sponge state. This study thus opens up a new avenue for the development of novel smart molecular switches at the device level.

Understanding Antiferromagnetic and Ligand Field Effects on Spin Crossover in a Triple-Decker Dimeric Cr(II) Complex.

Two possible explanations for the temperature dependence of spin-crossover (SCO) behavior in the dimeric triple-decker Cr(II) complex ([(η5-C5Me5)Cr(μ2:η5-P5)Cr(η5-C5Me5)]+) have been offered. One invokes variations in antiferromagnetic interactions between the two Cr(II) ions, whereas the other posits the development of a strong ligand-field effect favoring the low-spin ground state. We perform multireference electronic structure calculations based on the multiconfiguration pair-density functional theory to resolve these effects. We find quintet, triplet, and singlet electronic ground states, respectively, for the experimental geometries at high, intermediate, and low temperatures. The ground-state transition from quintet to triplet at an intermediate temperature derives from increased antiferromagnetic interactions between the two Cr(II) ions. By contrast, the ground-state transition from triplet to singlet at low temperature can be attributed to increased ligand-field effects, which dominate with continued variations in antiferromagnetic coupling. This study provides quantitative detail for the degree to which these two effects can act in concert for the observed SCO behavior in this complex and others subject to temperature-dependent variations in geometry.

Exploring spin states by hybrid functional methods to define correct trends in electrocatalytic activity of SACs embedded in N-doped graphene

Embedding transition metal atoms in graphene is a promising strategy to make it an effective electrocatalyst for the oxygen evolution (OER) and reduction (ORR) reactions, which are crucial processes for the success of the energy transition. In this regard, theoretical investigations can be valuable complementary tools to experimental work, but only if they are able to adequately describe the system under examination. Transition metal atoms trapped in graphene pose serious challenges due to the presence of strongly correlated d-electrons, which can lead to complex spin configurations to be explored. In this work, by hybrid density functional theory (DFT) calculations we investigated several first-row transition metal atoms embedded in N-doped graphene as potential electrocatalysts for the OER and ORR. A detailed spin-dependent search has been performed to define the lowest energy spin state configurations for all intermediates along the associative path, finding Ni and Fe as the most promising systems for the OER and ORR, based on overpotential values (η) of 0.58 V and 0.52 V, respectively. Interestingly, if the study is limited to low-spin configurations, the resulting overpotential values differ within the range of 0.5 V, changing the order of activity between the various electrocatalytic systems. The most striking case is that of Fe, where according to the low-spin state reaction path it would suggest this to be the worst electrocatalyst for ORR. Thus, this work conveys a very important message and general warning to the community on trusting only data that come from a full spin optimization.

Elucidation of the mechanistic origin of spin-state-dependent P-doped Fe single-atom catalysts for the oxidation of organic pollutants through peroxymonosulfate activation

In this study, the Fe single-atom catalyst (Fe-NC) was decorated via electronic structure modulation strategy and P was introduced into the second shell layer to improve the ability for peroxymonosulfate (PMS) activation. The Fe-PNC exhibits outstanding activity for bisphenol A (BPA) oxidation ascribed to its unique coordination environment (Fe-N4P2) and high spin state in comparison with Fe-NC (Fe-N4, low spin state) supported by the experimental data and density functional theory (DFT) calculations. We demonstrate that the higher energy of Fe 3d orbitals could better overlap with the O 2p orbitals of PMS, facilitating the electron transfer from Fe sites to PMS. In addition, P doping lowered the splitting field energy of the ligand and the energy gap between the contaminant and the catalyst, accelerating the transfer electrons from the adsorbed contaminant to the Fe site, thus maintaining the high spin state of Fe site and improving the stability of catalysis.

Increasing the number of modulated Fe single-atom sites by adjacent nanoparticles for efficient oxygen reduction with spin-state transition

Utilizing the nanoparticles (NPs) to improve the oxygen reduction reaction (ORR) performance of Fe single atoms (SAs) is conducive, but it is far from further application due to its limited number of enhanced SAs site and unclear origin of the enhanced electrocatalytic activity. Herein, we develop a hybrid catalyst contains a high density of activated SAs and explored the origin of this excellent activity. In the hybrid catalyst, the isolated Fe SAs are clustered within 2 nm around CFe2.5NPs ((CFe2.5)NP/FeSA-N-C), implying that these Fe SAs active sites are being modulated and enhanced. Further theory reveals those strong interactions between Fe SAs and adjacent CFe2.5 NPs induces transition of spin-polarization configuration of Fe centers from high spin state to low spin state, leading to weakened bonding strength of Fe atoms and OOH*. The optimized (CFe2.5)NP/FeSA-N-C possesses a superior ORR performance, and exhibits an amazing application potential in zinc-air batteries.

Controlling Spin Crossover in a Family of Dinuclear Fe(III) Complexes via the Bis(catecholate) Bridging Ligand.

Spin crossover (SCO) complexes can reversibly switch between low spin (LS) and high spin (HS) states, affording possible applications in sensing, displays, and molecular electronics. Dinuclear SCO complexes with access to [LS-LS], [LS-HS], and [HS-HS] states may offer increased levels of functionality. The nature of the SCO interconversion in dinuclear complexes is influenced by the local electronic environment. We report the synthesis and characterization of [{FeIII(tpa)}2spiro](PF6)2 (1), [{FeIII(tpa)}2Br4spiro](PF6)2 (2), and [{FeIII(tpa)}2thea](PF6)2 (3) (tpa = tris(2-pyridylmethyl)amine, spiroH4 = 3,3,3',3'-tetramethyl-1,1'-spirobi(indan)-5,5',6,6'-tetraol, Br4spiroH4 = 3,3,3',3'-tetramethyl-1,1'-spirobi(indan)-4,4',7,7'-tetrabromo-5,5',6,6'-tetraol, theaH4 = 2,3,6,7-tetrahydroxy-9,10-dimethyl-9,10-dihydro-9,10-ethanoanthracene), utilizing non-conjugated bis(catecholate) bridging ligands. In the solid state, magnetic and structural analysis shows that 1 remains in the [HS-HS] state, while 2 and 3 undergo a partial SCO interconversion upon cooling from room temperature involving the mixed [LS-HS] state. In solution, all complexes undergo SCO from [HS-HS] at room temperature, via [LS-HS] to mixtures including [LS-LS] at 77 K, with the extent of SCO increasing in the order 1 < 2 < 3. Gas phase density functional theory calculations suggest a [LS-LS] ground state for all complexes, with the [LS-HS] and [HS-HS] states successively destabilized. The relative energy separations indicate that ligand field strength increases following spiro4- < Br4spiro4- < thea4-, consistent with solid-state magnetic and EPR behavior. All three complexes show stabilization of the [LS-HS] state in relation to the midpoint energy between [LS-LS] and [HS-HS]. The relative stability of the [LS-HS] state increases with increasing ligand field strength of the bis(catecholate) bridging ligand in the order 1 < 2 < 3. The bromo substituents of Br4spiro4- increase the ligand field strength relative to spiro4-, while the stronger ligand field provided by thea4- arises from extension of the overlapping π-orbital system across the two catecholate units. This study highlights how SCO behavior in dinuclear complexes can be modulated by the bridging ligand, providing useful insights for the design of molecules that can be interconverted between more than two states.

Surface-Induced Electronic and Vibrational Level Shifting of [Fe(py)2bpym(NCS)2] on Al(100).

It is essential that one understands how the surface degrees of freedom influence molecular spin switching to successfully integrate spin crossover (SCO) molecules into devices. This study uses density functional theory calculations to investigate how spin state energetics and molecular vibrations change in a Fe(II) SCO compound named [Fe(py)2bpym(NCS)2] when deposited on an Al(100) surface. The calculations consider an environment-dependent U to assess the local Coulomb correlation of 3d electrons. The results show that the adsorption configurations heavily affect the spin state splitting, which increases by 10-40 kJmol-1 on the surface, and this is detrimental to spin conversion. This effect is due to the surface binding energy variation across the spin transition. The preference for the low-spin state originates partly from the strong correlation effect. Furthermore, the surface environment constrains the vibrational entropy difference, which decreases by 8-17 Jmol-1K-1 (at 300 K) and leads to higher critical temperatures. These results suggest that the electronic energy splitting and vibrational level shifting are suitable features for characterizing the spin transition process on surfaces, and they can provide access to high-throughput screening of spin crossover devices.

Combined Experimental and Mechanoelastic Modeling Studies on the Low-Spin Stabilized Mixed Crystals of 3D Oxalate-Based Coordination Materials.

Structural studies involving single-crystal and powder X-ray diffraction analysis have been performed on dehydrated coordination networks of the [NixCo1-x(bpy)3][LiCr(ox)3] series, 0 ≤ x ≤ 1, (bpy = 2,2'-bipyridine). The high-symmetry cubic 3D structure of these materials is formed by oxalate anions bridging alternating Cr3+ and Li+ ions into an anionic framework, which contains large cavities that incorporate the [NixCo1-x(bpy)3]2+ cations. Irrespective of the Co/Ni ratio, all of the mixed samples are phase-pure and retain the high-symmetry cubic structure, with the lattice parameters gradually decreasing upon increasing Ni(II) concentration. The influence of the Ni(II) dilution on the magnetic behavior of these materials is substantial. For pure [Co(bpy)3][LiCr(ox)3], a gradual but incomplete thermal spin-crossover is evident due to the effect of the chemical pressure applied by the [LiCr(ox)3]2- framework, which stabilizes the low-spin (LS) 2E state relative to the high-spin (HS) 4T1 state of the Co(II) ion. Upon increasing the Ni(II) content, the spin-crossover becomes even more gradual and incomplete and eventually is not observed for pure [Ni(bpy)3][LiCr(ox)3]. The average spin-crossover temperature increases with the increasing Ni(II) content, suggesting a higher degree of chemical pressure applied by the oxalate framework manifested by changing the ΔE0HL toward positive values. The magnetic behavior of all these framework materials has been explained by the mechanoelastic model, considering different radii for Co and Ni molecules and different interactions between Co-Co sites and Co-Ni sites. The model reproduced the incomplete transition, with the HS residual fraction at 300 K decreasing with increasing Ni concentration, and provided microscopic snapshots of the systems, showing how the existence of impurities prevented the spreading of Co atoms in the HS state.

Influence of oxygen stoichiometry on [formula omitted] spin state transitions and magnetic properties in [formula omitted] cobaltites

The layered EuBaCo2O5+δ (δ= 0.47) (EBCO) cobaltite shows various magnetic phases at high temperature and magnetic glassy state at low temperature. Further, the various magnetic phases of the EBCO are coupled with the spin state transition of Co3+ octahedra. In the present study, we report the structural and magnetization properties of the EBCO by changing the oxygen stoichiometry. The various oxygen compositions were obtained after post annealing the as-prepared EBCO cobaltite under argon and oxygen atmospheres and the final stoichiometry was detected from the iodometric titrations. The δ= 0.13 and 0.67 samples show the tetragonal symmetry (space group, P4/mmm), whereas the δ= 0.41, 0.47 and 0.58 samples show the orthorhombic symmetry (space group, Pmmm). The magnetization measurements on the δ= 0.13 sample shows the paramagnetic to antiferromagnetic ordering at TN= 288 K and the electrical resistivity analysis shows the Co2+ and Co3+ charge ordering at TCO= 180 K. Further, the δ= 0.13 sample show the absence of the ferromagnetic phase and Co3+ spin state transitions. The δ= 0.58 and 0.67 samples show the coexistence of ferromagnetic and antiferromagnetic phases, however, the features of Co3+ intermediate spin (IS) to low spin (LS) state transition is suppressed, which is observed in δ= 0.47 sample at 151 K. Our results indicate a tuning of the crystal structure along with the magnetic properties and also the Co3+ spin state transitions by oxygen stoichiometry variation in EuBaCo2O5+δ cobaltites.

High-Spin Blatter's Triradicals.

Robust organic triradicals with high-spin quartet ground states provide promising applications in molecular magnets, spintronics, etc. In this context, a triradical based on Blatter's radical has been synthesized recently, having two low-lying non-degenerate doublet states with a quartet ground state. The traditional broken-symmetry (BS)-DFT computed doublet-quartet energy gaps are reported to be somewhat overestimated in comparison to the experimentally observed values. In this work, we have employed different ab initio methods on this prototypical system to obtain more accurate doublet-quartet energy gaps for this triradical. The spin-constraint broken-symmetry (CBS)-DFT method has been used to reduce the overestimation of energy gaps from BS-DFT. To address the issues of spin-contamination and the multireference nature of low-spin states affecting the DFT methods, we have computed the energy gaps using appropriately state-averaged CASSCF and NEVPT2 computations. Using a series of active spaces, our calculations are shown to provide quite accurate values in concordance with the experimentally observed results. Furthermore, we have proposed and modeled another two triradicals based on Blatter's radical, which are of interest for experimental synthesis and characterization. Our computations show that all these triradicals also have a quartet ground state with a similar energy difference between the excited doublet states.

BEG spin-1 model with random exchange magnetic interactions for spin-crossover solids

We have investigated magnetic phase diagrams of spin-crossover (SCO) solids throughout the Blume–Emery–Griffiths spin-1 model where the spin states ±1 and 0 are associated to high-spin state and low-spin states respectively. In the present work, the quadrupolar interaction, K, parameter depends linearly on temperature and accounts for the role of the lattice phonons in the elastic interactions between the SCO units. Magnetic interactions are randomly distributed in the system and are controlled by a factor such that for γ = 0 (), magnetic ordering is not expected. The crystal-field that acts on SCO sites depends both on the ligand-field strength and the degeneracy ratio between HS and LS states as in some previous works. The system is also under the effect of a random local magnetic field hi acting on each site i. The model is solved using a homogeneous mean field theory. Our investigations reveal the occurrence of thermally-induced gradual, and first-order spin-transitions by varying the model parameters. At vicinity of first-order transition, various types of isothermal magnetic hysteresis loops are obtained and their corresponding coercive field and loop patterns are discussed as function of temperature.

Characterization of the active site in the thiocyanate-forming protein from Thlaspi arvense (TaTFP) using EPR spectroscopy.

Glucosinolates are plant thioglucosides, which act as chemical defenses. Upon tissue damage, their myrosinase-catalyzed hydrolysis yields aglucones that rearrange to toxic isothiocyanates. Specifier proteins such as thiocyanate-forming protein from Thlaspi arvense (TaTFP) are non-heme iron proteins, which capture the aglucone to form alternative products, e.g. nitriles or thiocyanates. To resolve the electronic state of the bound iron cofactor in TaTFP, we applied continuous wave electron paramagnetic resonance (CW EPR) spectroscopy at X-and Q-band frequencies (∼9.4 and ∼34 GHz). We found characteristic features of high spin and low spin states of a d 5 electronic configuration and local rhombic symmetry during catalysis. We monitored the oxidation states of bound iron during conversion of allylglucosinolate by myrosinase and TaTFP in presence and absence of supplemented Fe2+. Without added Fe2+, most high spin features of bound Fe3+ were preserved, while different g'-values of the low spin part indicated slight rearrangements in the coordination sphere and/or structural geometry. We also examined involvement of the redox pair Fe3+/Fe2 in samples with supplemented Fe2+. The absence of any EPR signal related to Fe3+ or Fe2+ using an iron-binding deficient TaTFP variant allowed us to conclude that recorded EPR signals originated from the bound iron cofactor.