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Reversible guest-induced gate-opening with multiplex spin crossover responses in two-dimensional Hofmann clathrates.

ABSTRACT: Spin crossover (SCO) compounds are very attractive types of switchable materials due to their potential applications in memory devices, actuators or chemical sensors. Rational chemical tailoring of these switchable compounds is key for achieving new functionalities in synergy with the spin state change. However, the lack of precise structural information required to understand the chemical principles that control the SCO response with external stimuli may eventually hinder further development of spin switching-based applications. In this work, the functionalization with an amine group in the two-dimensional (2D) SCO compound {Fe(5-NH₂Pym)₂[M^II(CN)₄]} (1M, 5-NH₂Pym = 5-aminopyrimidine, M^II = Pt (1Pt), Pd (1Pd)) confers versatile host-guest chemistry and structural flexibility to the framework primarily driven by the generation of extensive H-bond interactions. Solvent free 1M species reversibly adsorb small protic molecules such as water, methanol or ethanol yielding the 1M·H2O, 1M·0.5MeOH or 1M·xEtOH (x = 0.25-0.40) solvated derivatives. Our results demonstrate that the reversible structural rearrangements accompanying these adsorption/desorption processes (1M ↔ 1M·guest) follow a gate-opening mechanism whose kinetics depend not only on the nature of the guest molecule and that of the host framework (1Pt or 1Pd) but also on their reciprocal interactions. In addition, a predictable and reversible guest-induced SCO modulation has been observed and accurately correlated with the associated crystallographic transformations monitored in detail by single crystal X-ray diffraction.

SUBMITTER: Turo-Cortes R

PROVIDER: S-EPMC8162911 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Increasing spin crossover cooperativity in 2D Hofmann-type materials with guest molecule removal.

Project description:Molecule-based spin state switching materials that display ambient temperature transitions with accompanying wide thermal hysteresis offer an opportunity for electronic switching, data storage, and optical technologies but are rare in existence. Here, we present the first 2D Hofmann-type materials to exhibit the elusive combination of ambient temperature spin crossover with wide thermal hysteresis (ΔT = 50 and 65 K). Combined structural, magnetic, spectroscopic, and theoretical analyses show that the highly cooperative transition behaviours of these layered materials arise due to strong host-host interactions in their interdigitated lattices, which optimises long-range communication pathways. With the presence of water molecules in the interlayer pore space in the hydrated phases, competing host-host and host-guest interactions occur, whilst water removal dramatically increases the framework cooperativity, thus affording systematic insight into the structural features that favour optimal spin crossover properties.

| S-EPMC6048833 | biostudies-literature

Reversible quantitative guest sensing via spin crossover of an iron(ii) triazole.

Project description:A new phenyl-triazole-pyrazine ligand, 4-p-tolyl-3-(phenyl)-5-(2-pyrazinyl)-1,2,4-triazole (tolpzph), was prepared in order to enforce pyrazine coordination of the iron(ii) centre in the resulting complex, [FeII(tolpzph)2(NCS)2]·THF (1·THF). Structure determinations carried out on this discrete mononuclear complex, 1·THF, at 273 K (mostly high spin) and 100 K (mostly low spin) demonstrate this was successful, and that spin crossover (SCO) occurred on cooling. Subsequent magnetic measurements on 1·THF revealed that it shows highly sensitive and reversible solvent-dependent SCO, with T1/2(1·THF) = 255 K vs. T1/2(1) = 212 K (with SCO of 1 more abrupt and occurring with a 4 K hysteresis loop), a drop of 43 K due to THF loss. This is reversible over at least 10 cycles of re-solvating with THF followed by re-drying, so 1 ↔ 1·THF can be considered an 'on-off' THF sensor, monitored by the T1/2 reversibly shifting (by 43 K). Furthermore, quantitative sensing of the fractional amount of THF present in 1·nTHF, 0 ≤ n ≤ 1, is demonstrated. Monitoring the T1/2 and using TGA to quantify n(THF) revealed a linear dependence (25 data points; Pearson r2 = 0.93): T1/2 = 41.1n(THF) + 219. Finally, 1 is also shown to take up CHCl3 [T1/2(1·CHCl3) = 248 K], with a logarithmic T1/2 dependence on the fractional amount of CHCl3 present (10 data points; Pearson r2 = 0.98): T1/2 = 27.0 log10[n(CHCl3)] + 243. This study is a proof of principle that a (multi-use) quantitative sensor material based on spin crossover is feasible.

| S-EPMC5477032 | biostudies-literature

Iron(II) Complexes of 2,6-Di[4-(ethylcarboxy)pyrazol-1-yl]pyridine with Reversible Guest-Modulated Spin-Crossover Behavior.

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Bistable Hofmann-Type FeII Spin-Crossover Two-Dimensional Polymers of 4-Alkyldisulfanylpyridine for Prospective Grafting of Monolayers on Metallic Surfaces.

Project description:Aiming at investigating the suitability of Hofmann-type two-dimensional (2D) coordination polymers {FeII(Lax)2[MII(CN)4]} to be processed as single monolayers and probed as spin crossover (SCO) junctions in spintronic devices, the synthesis and characterization of the MII derivatives (MII = Pd and Pt) with sulfur-rich axial ligands (Lax = 4-methyl- and 4-ethyl-disulfanylpyridine) have been conducted. The thermal dependence of the magnetic and calorimetric properties confirmed the occurrence of strong cooperative SCO behavior in the temperature interval of 100-225 K, featuring hysteresis loops 44 and 32.5 K/21 K wide for PtII-methyl and PtII/PdII-ethyl derivatives, while the PdII-methyl derivative undergoes a much less cooperative multistep SCO. Excluding PtII-methyl, the remaining compounds display light-induced excited spin-state trapping at 10 K with TLIESST temperatures in the range of 50-70 K. Single-crystal studies performed in the temperature interval 100-250 K confirmed the layered structure and the occurrence of complete transformation between the high- and low-spin states of the FeII center for the four compounds. Strong positional disorder seems to be the source of elastic frustration driving the multistep SCO observed for the PdII-methyl derivative. It is expected that the peripheral disulfanyl groups will favor anchoring and growing of the monolayer on gold substrates and optimal electron transport in the device.

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Confinement inside MOFs Enables Guest-Modulated Spin Crossover of Otherwise Low-Spin Coordination Cages.

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Guest induced reversible on-off switching of elastic frustration in a 3D spin crossover coordination polymer with room temperature hysteretic behaviour.

Project description:A binary reversible switch between low-temperature multi-step spin crossover (SCO), through the evolution of the population γ HS(T) with high-spin (HS)-low-spin (LS) sequence: HS1LS0 (state 1) ↔ HS2/3LS1/3 (state 2) ↔ HS1/2LS1/2 (state 3) ↔ HS1/3LS2/3 (state 4) ↔ HS0LS1 (state 5), and complete one step hysteretic spin transition featuring 20 K wide thermal hysteresis centred at 290 K occurs in the three-dimensional (3D) Hofmann-type porous coordination polymer {FeII(3,8phen)[Au(CN)2]2}·xPhNO2 (3,8phen = 3,8-phenanthroline, PhNO2 = nitrobenzene), made up of two identical interpenetrated pcu-type frameworks. The included PhNO2 guest (x = 1, 1·PhNO2) acts as a molecular wedge between the interpenetrated 3D frameworks via PhNO2-3,8phen intermolecular recognition and is the source of the strong elastic frustration responsible for the multi-step regime. Detailed X-ray single crystal analysis reflects competition between spatial periodicities of structurally inequivalent HS and LS SCO centres featuring: (i) symmetry breaking (state 3) with ⋯HS-LS⋯ ordering with γ HS = 1/2; and (ii) occurrence of spatial modulation of the structure providing evidence for stabilization of local or aperiodic ordered mixed spin states for states 2 and 4 (with γ HS ≈ 2/3) and 4 (with γ HS ≈ 1/3), respectively. Below c.a. 20 K, structural and magnetic analyses show the photogeneration of a metastable HS*, state 6. The room-temperature single-step hysteretic regime appears with release of the guest (x = 0, 1) and the elastic frustration, and reversibly switches back to the original four-step behaviour upon guest re-adsorption. Both uncommon relevant SCO events meeting in the same material represent a rare opportunity to compare them in the frame of antiferro- and ferro-elastic transitions.

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Thermo- and photo-modulation of exciplex fluorescence in a 3D spin crossover Hofmann-type coordination polymer.

Project description:The search for bifunctional materials showing synergies between spin crossover (SCO) and luminescence has attracted substantial interest since they could be promising platforms for new switching electronic and optical technologies. In this context, we present the first three-dimensional FeII Hofmann-type coordination polymer exhibiting SCO properties and luminescence. The complex {FeII(bpben)[Au(CN)2]}@pyr (bpben = 1,4-bis(4-pyridyl)benzene) functionalized with pyrene (pyr) guests undergoes a cooperative multi-step SCO, which has been investigated by single crystal X-ray diffraction, single crystal UV-Vis absorption spectroscopy, and magnetic and calorimetric measurements. The resulting fluorescence from pyrene and exciplex emissions are controlled by the thermal and light irradiation (LIESST effect) dependence of the high/low-spin state population of FeII. Conversely, the SCO can be tracked by monitoring the fluorescence emission. This ON-OFF interplay between SCO and luminescence combined with the amenability of Hofmann-type materials to be processed at the nano-scale may be relevant for the generation of SCO-based sensors, actuators and spintronic devices.

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Redox and guest tunable spin-crossover properties in a polymeric polyoxometalate.

Project description:A bifunctionalized polyoxometalate (POM), [V6O19(C16H15N6O)2]2-, which contains a redox active hexavanadate moiety covalently linked to two tridentate 2,6-bis(pyrazol-1-yl)pyridine (1-bpp) ligands, has been prepared and characterized. Reaction of this hybrid molecule with Fe(ii) or Zn(ii) ions produces crystalline neutral 1D networks of formula Fe[V6O19(C16H15N6O)2]·solv (2) and Zn[V6O19(C16H15N6O)2]·solv (3) (solv = solvent molecules). Magnetic properties of 2 show an abrupt spin-crossover (SCO) with the temperature, which can be induced by light irradiation at 10 K (Light-Induced Excited Spin-State Trapping, LIESST effect). Interestingly, this porous and flexible structure enables reversible exchange of solvents in 2, which allows tuning the temperature of the thermal SCO. In 2 and 3, the hexavanadate unit can be reduced by electrochemical or chemical means in a reversible way. Chemical reduction and reoxidation by a postsynthetic method is accompanied by the insertion in the structure of the reductant and oxidant molecules (cobaltocene and tribromide, respectively), which provokes drastic changes in the spin state of Fe(ii). This leads to an elegant switching multifunctional material in which SCO properties of the Fe(ii) complexes coexist with the redox properties of the POM and can be tuned by a variety of stimuli such as temperature, light, solvent exchange or electron transfer. During the reduction process, 3 undergoes a single-crystal-to-single-crystal one-electron reduction, which confirms the presence of cobaltocenium cations by single crystal X-ray diffraction.

| S-EPMC10016358 | biostudies-literature

Spin-crossover modulation via single-crystal to single-crystal photochemical [2 + 2] reaction in Hofmann-type frameworks.

Project description:This study reports the first modulation of spin-crossover (SCO) behavior via a photochemical [2 + 2] cycloaddition reaction. Here we construct two no-solvent Fe(ii)-Ag(i) bimetallic Hofmann-type frameworks, [Fe(4-spy)2{Ag(CN)2}2] (1) and [Fe(2,4-bpe)2{Ag(CN)2}2] (2) (4-spy = 4-styrylpyridine, 2,4-bpe = trans-1-(2-pyridyl)-2-(4-pyridyl)ethylene). For 1, the dimerization of 4-spy results in a single-crystal to single-crystal (SCSC) transformation from 2D interdigitated layers to a 3D interpenetrated structure. Additionally, a 3D ? 3D structural transformation accompanied with Ag(i)-N bond breaking is achieved via the photochemical cycloaddition reaction of 2,4-bpe in 2. More importantly, both the spin transition temperatures and the SCO character are effectively modulated; thus, this approach provides a new strategy for constructing photo-responsive SCO magnetic materials.

| S-EPMC6764279 | biostudies-literature

Dimensional crossover in a layered ferromagnet detected by spin correlation driven distortions.

Project description:Magneto-elastic distortions are commonly detected across magnetic long-range ordering (LRO) transitions. In principle, they are also induced by the magnetic short-range ordering (SRO) that precedes a LRO transition, which contains information about short-range correlations and energetics that are essential for understanding how LRO is established. However these distortions are difficult to resolve because the associated atomic displacements are exceedingly small and do not break symmetry. Here we demonstrate high-multipole nonlinear optical polarimetry as a sensitive and mode selective probe of SRO induced distortions using CrSiTe3 as a testbed. This compound is composed of weakly bonded sheets of nearly isotropic ferromagnetically interacting spins that, in the Heisenberg limit, would individually be impeded from LRO by the Mermin-Wagner theorem. Our results show that CrSiTe3 evades this law via a two-step crossover from two- to three-dimensional magnetic SRO, manifested through two successive and previously undetected totally symmetric distortions above its Curie temperature.

| S-EPMC6458139 | biostudies-literature

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