Self-Assembled Tetranuclear Square Complex of Chromium(III) Bridged by Radical Pyrazine: A Molecular Model for Metal-Organic Magnets.

The attractive electronic properties of metal-pyrazine materials─electrical conductivity, magnetic order, and strong magnetic coupling─can be tuned in a wide range depending on the metal employed, as well as its ligand-imposed redox environment. Using solvent-directed synthesis to control the dimensionality of such systems, a discrete tetranuclear chromium(III) complex, exhibiting a rare example of bridging radical pyrazine, has been prepared from chromium(II) triflate and neutral pyrazine. The strong antiferromagnetic interaction between CrIII (S = 3/2) and radical pyrazine (S = 1/2) spins, theoretically estimated at about -932 K, leads to a thermally isolated ST = 4 ground state, which remains the only populated state observable even at room temperature.

Chemical Manipulation of the Spin-Crossover Dynamics through Judicious Metal-Ion Dilution.

In 2019, our groups described a unique FeII complex, [Fe(2MeL)(NCBH3)2] (2MeL = N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)-1,2-ethanediamine) possessing a low-spin ground state that is not easily accessible due to the extremely slow dynamics of the high-spin to low-spin phase transition. Herein, we report the successful chemical manipulation of this spin-crossover (SCO) process through controlled metal-ion dilutions. The emergence or suppression of the thermally induced SCO behavior was observed depending on the radius of the metal ion used for the dilution (NiII or ZnII). Reversible photo-switching has been confirmed in all mixed-metal complexes whether the low-spin state is thermally accessible. Remarkably, the dilution with ZnII metal ions stabilizes HS FeII complexes with complete suppression of the thermally induced SCO process without destroying the reversible photoswitchability of the material.

Self-Assembly Synthesis of a [2]Catenane CoII Single-Molecule Magnet.

We describe herein the self-assembly synthesis of an octanuclear CoII [2]catenane {[Co4 (H2 L)6 ]2 16+ } formed by the mechanical interlocking of two {[Co4 (H2 L)6 ]8+ } rectangles of unprecedented topology. Subtle manipulation of the synthetic conditions allows the isolation of a mixed-valence [Co2 III /Co2 II ]10+ non-catenated rectangle. The CoII centers in the [2]catenane exhibit slow relaxation of their magnetic moment, i. e. single-molecule magnet properties, dominated by quantum tunneling and Raman relaxation processes. This work shows that metallo-supramolecular chemistry can precisely control the organization of single-molecule magnets in topologically complex arrangements.

Room-Temperature Magnetic Bistability in a Salt of Organic Radical Ions.

Cocrystallization of 7,7',8,8'-tetracyanoquinodimethane radical anion (TCNQ-•) and 3-methylpyridinium-1,2,3,5-dithiadiazolyl radical cation (3-MepyDTDA+•) afforded isostructural acetonitrile (MeCN) or propionitrile (EtCN) solvates containing cofacial π dimers of homologous components. Loss of lattice solvent from the diamagnetic solvates above 366 K affords a high-temperature paramagnetic phase containing discrete TCNQ-• and weakly bound π dimers of 3-MepyDTDA+•, as evidenced by X-ray diffraction methods and magnetic susceptibility measurements. Below 268 K, a first-order phase transition occurs, leading to a low-temperature diamagnetic phase with TCNQ-• σ dimer and π dimers of 3-MepyDTDA+•. This study reveals the first example of cooperative interactions between two different organic radical ions leading to magnetic bistability, and these results are central to the future design of multicomponent functional molecular materials.

Photoinduced Mo-CN Bond Breakage in Octacyanomolybdate Leading to Spin Triplet Trapping.

The photoinduced properties of the octacoordinated complex K4 MoIV (CN)8 ⋅2 H2 O were studied by theoretical calculations, crystallography, and optical and magnetic measurements. The crystal structure recorded at 10 K after blue light irradiation reveals an heptacoordinated Mo(CN)7 species originating from the light-induced cleavage of one Mo-CN bond, concomitant with the photoinduced formation of a paramagnetic signal. When this complex is heated to 70 K, it returns to its original diamagnetic ground state, demonstrating full reversibility. The photomagnetic properties show a partial conversion into a triplet state possessing significant magnetic anisotropy, which is in agreement with theoretical studies. Inspired by these results, we isolated the new compound [K(crypt-222)]3 [MoIV (CN)7 ]⋅3 CH3 CN using a photochemical pathway, confirming that photodissociation leads to a stable heptacyanomolybdate(IV) species in solution.

Atomic Scale Evidence of the Switching Mechanism in a Photomagnetic CoFe Dinuclear Prussian Blue Analogue.

Molecular complexes based on Prussian Blue analogues have recently attracted considerable interest for their unique bistable properties combined to ultimately reduced dimensions. Here, we investigate the first dinuclear FeCo complex exhibiting both thermal and photomagnetic bistability in the solid state. Through an experimental and theoretical approach combining local techniques-X-ray absorption spectroscopy (XAS), X-ray magnetic circular dichroism (XMCD), and ligand field multiplet calculations-we were able to evidence the changes occurring at the atomic scale in the electronic and magnetic properties. The spectroscopic studies were able to fully support at the atomic level the following conclusions: (i) the 300 K phase and the light-induced excited state at 4 K are both built from FeLSIII-CoHSII paramagnetic pairs with no apparent reorganization of the local structure, (ii) the 100 K phase is composed of FeLSII-CoLSIII diamagnetic pairs, and (iii) the light-induced excited state is fully relaxed at an average temperature of ≈50 K. In the paramagnetic phase at 2 K, XAS and XMCD reveal that both Fe and Co ions exhibit a rather large orbital magnetic moment (0.65 µB and 0.46 µB, respectively, under an external magnetic induction of 6.5 T), but it was not possible to detect a magnetic interaction between spin centers above 2 K.

Slow Dynamics of the Spin-Crossover Process in an Apparent High-Spin Mononuclear FeII Complex.

A mononuclear FeII complex that shows a high-spin (S=2) paramagnetic behavior at all temperatures (with standard temperature-scan rates, ≈1 K min-1 ) has, in fact, a low-spin (S=0) ground state below 100 K. This low-spin state is not easily accessible due to the extremely slow dynamics of the spin-crossover process-a full relaxation from the metastable high-spin state to the low-spin ground state takes more than 5 h below 80 K. Bidirectional photo-switching of the FeII state is achieved reproducibly by two selective irradiations (at 530-590 and 830-850 nm). The slow dynamics of the spin-crossover and the strong structural cooperativity result in a remarkably wide 95-K hysteresis loop induced by both temperature and selected light stimuli.

Multistability at Room Temperature in a Bent-Shaped Spin-Crossover Complex Decorated with Long Alkyl Chains.

An iron(II) pyridyl-benzohydrazonate-based complex decorated with long alkyl chains is reported as a rare spin-crossover compound displaying a wide thermal hysteresis spanning room temperature. On heating, this compound exhibits a spin transition between a LS ground state and an ordered HS-LS phase with symmetry breaking from monoclinic P21/n into orthorhombic P21212 space groups. During cooling, the compound first transits into a magnetically distinguishable HS-LS phase with monoclinic P21 symmetry before returning into the LS phase. Interconversion between the two distinct HS-LS phases is the result of subtle structural changes in the alkyl chains and produces a second minor thermal hysteresis that superposes to the large one. This unprecedented result shows that the combination of a conventional cooperative spin transition and ligand-driven magnetic changes can promote magnetic tristability at room temperature.

Irradiation Temperature Dependence of the Photomagnetic Mechanisms in a Cyanido-Bridged CuII2MoIV Trinuclear Molecule.

We report a new bimetallic cyanido-bridged trinuclear complex [CuII(enpnen)]2[MoIV(CN)8]·6.75H2O (1) (enpnen = N,N'-bis(2-aminoethyl)-1,3-propanediamine) that shows reversible photomagnetic effect. The photo-induced increase of magnetization is characterized by the irradiation temperature-dependent shapes of the χM T( T) plots and different magnetization values at low temperature in high magnetic field, suggesting multiple photoexcited states. The photomagnetic effect in 1 is explained through two possible processes simultaneously: the light-induced metal-to-metal charge transfer (MMCT) in the CuII-NC-MoIV pair and the light-induced excited spin-state trapping (LIESST) effect in MoIV center. A numerical model assuming the simultaneous existence of three possible states after irradiation: the MMCT CuI-NC-MoV-CN-CuII state, the LIESST CuII-NC-MoIVHS-CN-CuII state, and the ground-state CuII-NC-MoIVLS-CN-CuII was applied to the data and resulted in Cu-Mo exchange coupling constants J1MMCT = 11 cm-1 and J2LIESST = 109 cm-1 for the MMCT and LIESST mechanisms induced states, respectively. Fractions of respective states after irradiations at different temperatures were also calculated, shedding light on the influence of irradiation temperature on the photomagnetic mechanism. The proposed model can provide the interpretative framework for testing and refinement of the mechanism of photomagnetic effect in other coordination networks with cyanido-bridged Cu-[Mo(CN)8]4- linkages.

[OsF6 ]x- : Molecular Models for Spin-Orbit Entangled Phenomena.

Heavy 5d elements, like osmium, feature strong spin-orbit interactions which are at the origin of exotic physical behaviors. Revealing the full potential of, for example, novel osmium oxide materials ("osmates") is however contingent upon a detailed understanding of the local single-ion properties. Herein, two molecular osmate analogues, [OsF6 ]2- and [OsF6 ]- , are reported as model systems for Os4+ and Os5+ centers found in oxides. Using X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD) techniques, combined with state-of-the-art ab initio calculations, their ground state was elucidated; mirroring the osmium electronic structure in osmates. The realization of such molecular model systems provides a unique chemical playground to engineer materials exhibiting spin-orbit entangled phenomena.

Mononuclear Fe(II) Complexes Based on the Methylpyrazinyl-Diamine Ligand: Chemical-, Thermo- and Photocontrol of Their Magnetic Switchability.

Two new mononuclear Fe(II) complexes, [Fe(2MeLpz)(NCX)2] (L = N,N'-dimethyl-N,N'-bis((pyrazin-2-yl)methyl)-1,2-ethanediamine and X = S (1), BH3 (2)), have been synthesized and characterized by single-crystal X-ray diffraction, magnetic, optical reflectivity, and photomagnetic measurements. They have similar FeN6 coordination environments offered by the tetradentate ligand with a cis-α conformation and two NCX- coligands in cis positions. However, 1 and 2 have different molecular arrangements and crystal packings, and are isolated in orthorhombic Pbnb and monoclinic C2/c space groups, respectively. 1 remains in a high spin state (S = 2) over all temperatures while 2 undergoes a spin transition around 168 K with a small thermal hysteresis of about 0.4 K (at a temperature scan rate of 1.3 K min-1). This phase transition, which can also be optically detected due to the associated marked change of the sample color, occurs between two structurally characterized phases, which exhibit Fe(II) complexes in their high spin and low spin states at high and low temperatures, respectively. The reversible photoswitching between these two states has also been confirmed at low temperatures using well separated wavelength irradiations.

Heterometallic Heptanuclear [Cu5Ln2] (Ln = Tb, Dy, and Ho) Single-Molecule Magnets Organized in One-Dimensional Coordination Polymeric Network.

The reaction of a multisite coordination ligand, LH3, with Cu(II) salts and Ln(NO3)3·nH2O in a 1:2:1 stoichiometric ratio in the presence of triethylamine was found to afford a series of one-dimensional heterometallic [{Cu5Ln2(L)2(µ3-OH)4(ClO4)(NO3)3(OH2)5}(ClO4)2(H2O)x]∞ [Ln = Tb(1), Dy(2) and Ho(3), x = 4.25, 5.5, and 5 for 1-3, respectively] coordination polymers. Complexes 1-3 have been characterized by single crystal X-ray crystallography. The detailed study of the magnetic properties has also been performed and compared with the parent [Cu5Ln2] molecular analogues. The ac susceptibility measurements for complexes 1-3 confirm their SMM behavior with the following characteristics: Δeff/kB = 23.4 K, τ0 = 1.1 × 10-6 s and Δeff/kB = 27.9 K, τ0 = 6.6 × 10-7 s under 0 and 1200 Oe dc fields, respectively for 1; Δeff/kB = 8.3 K, τ0 = 3.1 × 10-6 s for 2 under 0 dc field. For 3, the fast QTM below 4 K prevents the estimation of the SMM energy barrier. Remarkably, the magnetic and SMM properties of the previously reported molecular [Cu5Ln2] analogues are preserved after their assembly in these coordination networks.

Switchable Fe/Co Prussian blue networks and molecular analogues.

With the long term objective to build the next generation of devices from the molecular scale, scientists have explored extensively in the past two decades the Prussian blue derivatives and their remarkable physico-chemical properties. In particular, the exquisite Fe/Co system displays tuneable optical and magnetic behaviours associated with thermally and photo-induced metal-to-metal electron transfer processes. Recently, numerous research groups have been involved in the transfer of these electronic properties to new Fe/Co coordination networks of lower dimensionality as well as soluble molecular analogues in order to facilitate their manipulation and integration into devices. In this review, the most representative examples of tridimensional Fe/Co Prussian blue compounds are described, focusing on the techniques used to understand their photomagnetic properties. Subsequently, the different strategies employed toward the design of new low dimensional Prussian blue analogues based on a rational molecular building block approach are discussed emphasizing the advantages of these functional molecular systems.

Solvent-Triggered Cis/Trans Isomerism in Cobalt Dioxolene Chemistry: Distinguishing Effects of Packing on Valence Tautomerism.

In this article, the synthesis and X-ray crystal structures of two cis/trans isomers of valence tautomeric (VT) cobalt dioxolene compounds are reported. The cis isomer (1) was isolated from the polar protic methanol solvent as a kinetic product, whereas the less polar nonprotic solvent acetone yielded the trans isomer (2). It should be noted that, although some coordination polymers involving cobalt bis(dioxolene) with the cis disposition are known for bridging ancillary ligands, such an arrangement is unprecedented for mononuclear compounds. A careful study of intermocular interactions revealed that the methanol solvent does not have much influence on the crystal growth in 1, whereas acetone forms strong halogen-bonding interactions that are crucial in the solid-state architecture of 2. This behavior can likely be used in crystal engineering to design new organic-inorganic hybrid materials. The energy difference between the two isomers was examined using DFT calculations, confirming that the trans form is in the thermodynamic state whereas the cis isomer is a kinetic product that can be converted into the trans isomer with time. Finally, both isomers exhibit solvent loss at elevated temperatures that is accompanied by a change in magnetic properties, associated with an irreversible valence tautomerism. Our results highlight the crucial role of the solvents for the isolation of cis/trans isomers in cobalt dioxolene chemistry, as well as the distinguishing effects of intermolecular forces and the solid-state packing on VT behavior.

Large Orbital Magnetic Moment Measured in the [TpFe(III)(CN)3](-) Precursor of Photomagnetic Molecular Prussian Blue Analogues.

Photomagnetism in three-dimensional Co/Fe Prussian blue analogues is a complex phenomenon, whose detailed mechanism is not yet fully understood. Recently, researchers have been able to prepare molecular fragments of these networks using a building block synthetic approach from mononuclear precursors. The main objective in this strategy is to isolate the smallest units that show an intramolecular electron transfer to have a better understanding of the electronic processes. A prior requirement to the development of this kind of system is to understand to what extent electronic and magnetic properties are inherited from the corresponding precursors. In this work, we investigate the electronic and magnetic properties of the FeTp precursor (N(C4H9)4)[TpFe(III)(CN)3], (Tp being tris-pyrazolyl borate) of a recently reported binuclear cyanido-bridged Fe/Co complex. X-ray absorption spectroscopy and X-ray magnetic circular dichroism measurements at the Fe L2,3 edges (2p → 3d) supported by ligand field multiplet calculations have allowed to determine the spin and orbit magnetic moments. Inaccuracy of the spin sum rule in the case of low-spin Fe(III) ion was demonstrated. An exceptionally large value of the orbital magnetic moment is found (0.9 µB at T = 2 K and B = 6.5 T) that is likely to play an important role in the magnetic and photomagnetic properties of molecular Fe/Co Prussian blue analogues.

Direct C-N Coupling in an in Situ Ligand Transformation and the Self-Assembly of a Tetrametallic [Ni(II)4] Staircase.

A [Ni(II)4] staircase complex was serendipitously prepared from the reaction of the binucleating Schiff base proligand 2,6-bis[[(3-hydroxypropyl)imino]methyl]-4-methylphenol (H3L2) and 3,5-dimethylpyrazole (Me2pzH) with nickel(II) nitrate in a reaction at room temperature, initially aimed to yield a dinuclear complex. From a room temperature metal ion/ligand reaction, the proligand H3L2 in situ transformed to modified forms HL3(2-) and HL4(2-), allowing the [Ni4] formation. Variable-temperature magnetic behavior of a [Ni4] complex reveals antiferromagnetic interactions with stabilization of a diamagnetic ground state (ST = 0).

Thermochromic and photoresponsive cyanometalate Fe/Co squares: toward control of the electron transfer temperature.

Two structurally related and photoresponsive cyanide-bridged Fe/Co square complexes, {Fe2Co2}, are reported: {[(Tp(Me))Fe(CN)3]2[Co(bpy)2]2[(Tp(Me))Fe(CN)3]2}·12H2O (2) and {[(Tp(Me))Fe(CN)3]2[Co(bpy)2]2[BPh4]2}·6MeCN (3), where Tp(Me) and bpy are hydridotris(3-methylpyrazol-1-yl)borate and 2,2'-bipyridine, respectively. Through electrochemical and spectroscopic studies, the Tp(Me) ligand appears to be a moderate σ donor in comparison to others in the [NEt4][(Tp(R))Fe(III)(CN)3] series [where Tp(R) = Tp, hydridotris(pyrazol-1-yl)borate; Tp(Me) = hydridotris(3-methylpyrazol-1-yl)borate; pzTp = tetrakis(pyrazol-1-yl)borate; Tp* = hydridotris(3,5-dimethylpyrazol-1-yl)borate; Tp*(Me) = hydridotris(3,4,5-trimethylpyrazol-1-yl)borate]. The spectroscopic, structural, and magnetic data of the {Fe2Co2} squares indicate that thermally-induced intramolecular electron transfer reversibly converts {Fe(II)LS(µ-CN)Co(III)LS} pairs into {Fe(III)LS(µ-CN)Co(II)HS} units near ca. 230 and 244 K (T1/2) for 2 and 3, respectively (LS: low spin; HS: high spin). These experimental results show that 2 and 3 display light-induced {Fe(III)LS(µ-CN)Co(II)HS} metastable states that relax to thermodynamic {Fe(II)LS(µ-CN)Co(III)LS} ones at ca. 90 K. Ancillary Tp(R) ligand donor strength appears to be the dominant factor for tuning electron transfer properties in these {Fe2Co2} complexes.

Metal-to-metal electron transfer in Co/Fe Prussian Blue molecular analogues: the ultimate miniaturization.

Co/Fe Prussian Blue analogues are known to display both thermally and light induced electron transfer attributed to the switching between diamagnetic {Fe(II)LS(µ-CN)Co(III)LS} and paramagnetic {Fe(III)LS(µ-CN)Co(II)HS} pairs (LS = low spin; HS = high spin). In this work, a dinuclear cyanido-bridged Co/Fe complex, the smallest {Fe(µ-CN)Co} moiety at the origin of the remarkable physical properties of these systems, has been designed by a rational building-block approach. Combined structural, spectroscopic, magnetic and photomagnetic studies reveal that a metal-to-metal electron transfer that can be triggered in solid state by light, temperature and solvent contents, is observed for the first time in a dinuclear complex.

Chiral (LH)2L2Cu3 trinuclear paramagnetic nodes in octacyanidometalate-bridged helical chains.

Trinuclear chiral (LH)2L2Cu3 (LH = 1,3-diamino-2-propanol, bdapH) assemblies linked by octacyanidometalate(IV) form isostructural one-dimensional (1D) chains consisting of right- and left-handed helixes arranged in an alternate manner: [(bdapH)2(bdap)2Cu(II)3][M(IV)(CN)8]·H2O (M = Mo 1, W 2). Each chain displays helicity with a long pitch around 17.2 Å. The direction of the helix rotation is strictly connected with the conformation of the (LH)2L2Cu3 unit. Right-handed helixes are based on Δ-S,S-(LH)2L2Cu3, whereas left-handed ones contain Λ-R,R-(LH)2L2Cu3 units. Magnetic studies reveal antiferromagnetic interactions through alkoxo-bridges inside trinuclear Cu(II) nodes leading to an ST = 1/2 ground state for both assemblies.

Photoinduced single-molecule magnet properties in a four-coordinate iron(II) spin crossover complex.

The four-coordinate Fe(II) complex, PhB(MesIm)3Fe-N═PPh3 (1) has been previously reported to undergo a thermal spin-crossover (SCO) between high-spin (HS, S = 2) and low-spin (LS, S = 0) states. This complex is photoactive below 20 K, undergoing a photoinduced LS to HS spin state change, as determined by optical reflectivity and photomagnetic measurements. With continuous white light irradiation, 1 displays slow relaxation of the magnetization, i.e. single-molecule magnet (SMM) properties, at temperatures below 5 K. This complex provides a structural template for the design of new photoinduced mononuclear SMMs based on the SCO phenomenon.