Chiral Resolution of Spin-Crossover Active Iron(II) [2x2] Grid Complexes

Chiral magnetic materials are proposed for applications in second-order non-linear optics, magneto-chiral dichroism, among others. Recently, we have reported a set of tetra-nuclear Fe(II) grid complex conformers with general formula C/S-[Fe4L4]$^{8+}$ (L: 2,6-bis(6-(pyrazol-1-yl)pyridin-2-yl)-1,5-dihydrobenzo[1,2-d : 4,5-d′]diimidazole). In the grid complexes, isomerism emerges from tautomerism and conformational isomerism of the ligand L, and the S-type grid complex is chiral, which originates from different non-centrosymmetric spatial organization of the trans type ligand around the Fe(II) center. However, the selective preparation of an enantiomerically pure grid complex in a controlled manner is difficult due to spontaneous self-assembly. To achieve the pre-synthesis programmable resolution of Fe(II) grid complexes, we designed and synthesized two novel intrinsically chiral ligands by appending chiral moieties to the parent ligand. The complexation of these chiral ligands with Fe(II) salt resulted in the formation of enantiomerically pure Fe(II) grid complexes, as unambiguously elucidated by CD and XRD studies. The enantiomeric complexes exhibited similar gradual and half-complete thermal and photo-induced SCO characteristics. The good agreement between the experimentally obtained and calculated CD spectra further supports the enantiomeric purity of the complexes and even the magnetic studies. The chiral resolution of Fe(II)- [2×2] grid complexes reported in this study, for the first time, might enable the fabrication of magneto-chiral molecular devices

Abrupt Spin Crossover Behavior in a Linear N1,N2-Triazole Bridged Trinuclear Fe(II) Complex

The synthesis, structures and magnetic properties of a new trinuclear spin crossover complex [FeII3(pyrtrz)6(TsO)6]·10H2O·2CH3OH (C2) and its analogue binuclear [FeII2(pyrtrz)5(SCN)4]·7H2O (C1), are reported here. These two compounds are synthesized based on the pyrrolyl functionalized Schiff base 1,2,4-triazole ligand 4-((1H-pyrrol-2-yl)methylene-amino)-4H-1,2,4-triazole (pyrtrz), which represent rare discrete multi-nuclear species, with µ2-N1,N2-triazole bridges linking the FeII centers. DC magnetic susceptibility measurements revealed an abrupt single-step spin crossover (SCO) behavior for compound 2 on the central FeII site and single-crystal X-ray diffraction (173 K) showed that this compound crystallizes in the monoclinic space group (P21/c), and multiple intramolecular interactions were found responsible for the abrupt transition. Compound 1 is a binuclear complex with thiocyanate as terminal ligands. This compound stays in high spin state over the whole temperature range and displays weak antiferromagnetic exchange coupling

Vibrational properties and cooperativity of the 3D spin crossover network [Fe(pyrazine)][Pt(CN)4]\mathrm{[Fe(pyrazine)][Pt(CN)_{4}]}

Nuclear inelastic scattering of synchrotron radiation has been used to determine the phonon density of vibrational states (pDOS) for the high-spin and low-spin phases of the hydrated and dehydrated isomer of the spin crossover polymer [Fe(pyrazine)][Pt(CN)4]. Density functional theory calculations have been performed for molecular models of the 3D polymeric system. The models contain 15 Fe(II)/Zn(II) centres and allowed the assignment of the observed bands to the corresponding vibrational modes. Thermodynamic parameters like the mean force constant and the vibrational entropy but also sound velocities of the molecular lattices in both spin states have been derived from the pDOS. Modelling of the low-spin and high-spin centres in the environment or matrix of different spins has revealed the enthalpic and entropic components of the intramolecular cooperativity. In contrast to the 1D spin crossover systems (Rackwitz, et al., Phys. Chem. Chem. Phys., 2013, 15, 15450) based on the rigid 1,2,4-triazole derivatives the distortion of the low-spin iron Fe(II) centre by the matrix of high-spin Fe(II) (modelled as Zn(II)) occurs only in two dimensions, defined by the [M(CN)4]2− sheets, rather than concerning all six Fe–N bonds, as in 1D systems. The enthalpic intramolecular cooperativity has been determined to be 15 kJ mol−1 which is lower than that in 1D systems (20–30 kJ mol−1). Yet, the entropic contribution stabilizes the low-spin state in a low-spin matrix, a behaviour which is opposite to what was found for the 1D systems

Exploring the Vibrational Side of Spin‐Phonon Coupling in Single‐Molecule Magnets via 161Dy Nuclear Resonance Vibrational Spectroscopy

Bad vibrations? $^{161}$Dy nuclear resonance vibrational spectroscopy gives direct experimental access to the partial phonon density of states which includes all vibrational modes involving a displacement of the Dy$^{III}$ ion. In combination with density functional theory, an assignment to all intramolecular vibrational modes is possible, paving an ideal path to help to clarify the role of phonons in single-molecule magnets. Synchrotron-based nuclear resonance vibrational spectroscopy (NRVS) using the Mössbauer isotope $^{161}$Dy has been employed for the first time to study the vibrational properties of a single-molecule magnet (SMM) incorporating Dy$^{III}$, namely [Dy(Cy$_{3}$PO)$_{2}$(H$_{2}$O)$_{5}$]Br$_{3}$⋅2 (Cy$_{3}$PO)⋅2 H$_{2}$O ⋅2 EtOH. The experimental partial phonon density of states (pDOS), which includes all vibrational modes involving a displacement of the DyIII ion, was reproduced by means of simulations using density functional theory (DFT), enabling the assignment of all intramolecular vibrational modes. This study proves that $^{161}$Dy NRVS is a powerful experimental tool with significant potential to help to clarify the role of phonons in SMMs

Vibrational properties of the mononuclear Fe[HBpz3]2 spin crossover complex

Within this work, we report the results of nuclear inelastic scattering experiments of the low-spin phase of the iron(II) mononuclear SCO complex Fe[HBpz3]2 and density functional theory based calculations performed on a model molecule of the complex. We show that the calculated partial density of vibrational states based on the structure of a single iron(II) center which is linked by three pyrazole rings to borat is in good accordance with the experimentally obtained 57Fe-pDOS and assign the molecular vibrations to the prominent optical phonons

Vibrational properties of the mononuclear Fe[HBpz3_3]2_2 spin crossover complex

Within this work, we report the results of nuclear inelastic scattering experiments of the low-spin phase of the iron(II) mononuclear SCO complex Fe[HBpz$_3$]$_2$ and density functional theory based calculations performed on a model molecule of the complex. We show that the calculated partial density of vibrational states based on the structure of a single iron(II) center which is linked by three pyrazole rings to borat is in good accordance with the experimentally obtained $^{57}$Fe-pDOS and assign the molecular vibrations to the prominent optical phonons

Changes in the phonon density of states of Fe induced by external strain

Nuclear inelastic scattering of synchrotron radiation is used to study the changes induced by external tensile strain on the phonon density of states (pDOS) of polycrystalline Fe samples. The data are interpreted with the help of dedicated atomistic simulations. The longitudinal phonon peak at around 37 meV and also the second transverse peak at 27 meV are decreased under strain. This is caused by the production of defects under strain. Also the thermodynamic properties of the pDOS demonstrate a weakening of the force constants and of the mean phonon energy under strain. Remaining differences between experiment and simulation are discussed

Vibrational properties of 1D- and 3D polynuclear spin crossover Fe(II) urea-triazoles polymer chains and quantification of intrachain cooperativity

The vibrational dynamics of the iron centres in 1D and 3D spin crossover Fe(II) 4-alkyl-urea triazole chains have been investigated by synchrotron based nuclear inelastic scattering. For the 1D system, the partial density of phonon states has been modelled with density functional theory methods. Furthermore, spin dependent iron ligand distances and vibrational modes were obtained. The previously introduced intramolecular cooperativity parameter H$_{coop}$ (Rackwitz et al, Phys. Chem. Chem. Phys. 2013, 15, 15450) has been determined to −31 kJ mol$^{−1}$ for [Fe(n-Prtrzu)$_3$(tosylate)2] and to +27 kJ mol$^{−1}$ for [Fe(n-Prtrzu)$_3$(BF$_4$)$_2$]. The change of sign in Hcoop is in line with the incomplete and gradual character of the spin transition for the former as well as with the sharp transition for the latter reported previously (Rentschler and von Malotki, Inorg. Chem., Act. 2008, 361, 3646). This effect can be ascribed to the networks of intramolecular interactions in the second coordination sphere of the polymer chains, depending on the spin state of the iron centres. In addition, we observe a decreased coupling and coherence when comparing the system which displays a sharp spin transition to the system with an incomplete soft transition by analyzing molecular modes involving a movement of the iron centres

Mononuclear Fe(III) Schiff Base Complex with Trans-FeO₄N₂ Chromophore of <i>o</i>-Aminophenol Origin: Synthesis, Characterisation, Crystal Structure, and Spin State Investigation

A new iron(III) complex (Et3NH)2[Fe(L)2](ClO4)·MeOH (1) where H2L = 2-{(E)-[2-hydroxyphenyl)imino]methyl}phenol has been synthesised and characterised by single crystal XRD, elemental analysis and DC magnetic susceptibility measurements. The dianionic ligands L2− coordinate in a tridentate fashion with the Fe(III) through their deprotonated phenolic oxygens and azomethine nitrogen atoms, resulting in a trans-FeO4N2 chromophore. Variable-temperature magnetic measurements were performed between 300 and 5 K under an applied field of 0.1 T and show that 1 is in the high spin state (S = 5/2) over the whole measured temperature range. This is confirmed by Mössbauer spectroscopy at 77 and 300 K

Untersuchung von Schwingungen in Bezug auf Spin‐Phonon‐Kopplung in Einzelmolekülmagneten mittels nuklearer inelastischer Streuung am 161

Erstmalig wurde Synchrotron-basierte nukleare inelastische Streuung (NIS) unter Nutzung des Mößbauer-Isotops 161Dy für die Untersuchung der vibronischen Eigenschaften eines DyIII-basierten Einzelmolekülmagneten, [Dy(Cy3PO)2(H2O)5]Br3⋅2 (Cy3PO)⋅2 H2O⋅2 EtOH, eingesetzt. Die experimentelle partielle Phononen-Zustandsdichte, die alle Schwingungen mit einer Auslenkung des DyIII-Ions enthält, wurde mit Hilfe von auf Dichtefunktionaltheorie (DFT) basierenden Simulationen reproduziert, was die Zuordnung aller intramolekularen Schwingungsmoden des Moleküls ermöglicht. Diese Studie zeigt, dass 161Dy-NIS als eine experimentelle Methode ein hohes Potential besitzt, um zur Klärung der Rolle von Phononen in Einzelmolekülmagneten beizutragen