Energy Barrier For Relaxation Research Articles

Modulating the Magnetic Dynamics of Five‐Coordinate DyIII Single‐Molecule Magnets by the Substitution Effect on the Axial Ligand

AbstractTwo five‐coordinate mononuclear DyIII single‐molecule magnets [(TrapenTMS)Dy(L)] (Trapen=tris(2‐aminobenzyl) amine; TMS=SiMe3; L=OPMe3 1, OPEt3 2) have been synthesized by the reaction of [(TrapenTMS)Dy(THF)] and OPMe3, OPEt3, respectively. The molecular structures of 1 and 2 were fully established by single crystal X‐ray diffraction. The centre DyIII ions of both complexes exhibit distorted triangular bipyramid geometries, varying with different neutral ligands L on the apex. The TrapenTMS ligand forms the pyramid base of the trigonal bipyramid. Subtle structural modifications of the axial O‐ligand terminal substituent result in different dynamic magnetic behaviors. Magnetic data analysis reveals that 1 and 2 exhibit the characteristic behavior of SMM without a dc field, accompanying an unambiguous quantum tunneling of the magnetization. Field‐induced slow magnetic relaxation was observed for 1 and 2 under an applied bias dc field of 1000 Oe, the relaxation energy barriers are 107 K and 88 K for 1 and 2, respectively. We have investigated the differences in magnetism and magnetic anisotropy between the two complexes by ab initio calculations.

Anilato-Based Coordination Polymers with Slow Relaxation of the Magnetization: Role of the Synthetic Method and Anilato Ligand.

We have prepared and characterized three coordination polymers formulated as [Dy2(C6O4Cl2)3(fma)6] ⋅ 4.5fma (1) and [Dy2(C6O4X2)3(fma)6] ⋅ 4fma ⋅ 2H2O with X=Br (2) and Cl (3), where fma=formamide and C6O4X2 2-=3,6-disubstituted-2,5-dihydroxy-1,4-benzoquinone dianion with X=Cl (chloranilato) and Br (bromanilato). Compounds 1 and 3 are solvates obtained with slow and fast precipitation methods, respectively. Compounds 2 and 3 are isostructural and only differ in the X group of the anilato ligand. The three compounds present (6,3)-gon two-dimensional hexagonal honey-comb structures. Magnetic measurements indicate that the three compounds show slow relaxation of the magnetization at low temperatures when a continuous magnetic field is applied, although with different relaxation times and energy barriers depending on X and the crystallisation molecules. Compounds 1-3 represent the first examples of anilato-based lattices with formamide and field-induced slow relaxation of the magnetization.

Direct Observation of the Mutual Coupling Effect in the Protein-Water-Glycerol Mixture by Combining Neutron Scattering and Selective Deuteration.

Numerous studies have discussed the impact of cosolvents on the structure, dynamics, and stability of proteins in aqueous solutions. However, the dynamics of cosolvents in the protein-water-cosolvent ternary system is largely unexplored in experiments due to technical difficulty. Consequently, a comprehensive understanding of the interplay among proteins, water, and cosolvents is still lacking. Here, we employed selective deuteration and neutron scattering techniques to characterize the individual motions of each component in the protein/water/glycerol (GLY) mixture across various temperatures. The consistent dynamic onset temperatures and the correlation between the MSD of the protein and the viscosity of solvents revealed the mutual coupling effects among the three components. Furthermore, our experimental and simulation results showed that the hydrogen bond relaxation energy barrier in the ternary system is ∼43 kJ/mol, whereas in the protein-water binary system it is merely ∼35 kJ/mol. Therefore, we suggest that GLY can enhance hydrogen bond interactions in the ternary system through the mutual coupling effect, thereby serving as one of the protective mechanisms of protein preservation by GLY.

Photo-Activated Growth and Metastable Phase Transition in Metallic Solid Solutions.

Laser processing in metals is versatile yet limited by its reliance on phase transformation through heating rather than electronic excitation due to their low absorptivity, attributing from highly ordered structures. Metastable states (i.e., surfaces, glasses, undercooled liquids), however, present a unique platform, both energetically and structurally to enable energy landscape tuning through selective stimuli. Herein, this ansatz is demonstrated by exploiting thin passivating oxides to stabilize an undercooled state, followed by photo-perturbation of the near surface order to induce convective Marangoni flows, edge-coalescence and phase transition into a larger metastable solid bearing asymmetric composition between the near surface and core of the formed structure. The self-terminating nature of the process creates a perfectly contained system which can maintain a high relaxation energy barrier hence deep metastable states for extended periods of time.

ZnII-DyIII single-molecule magnets constructed by salen-type ligand, acetate and β-diketonate

A series of ZnII-DyIII complexes with molecular formula [LZn(CH3COO)Dy(hfac)2] (1), [LZn(CH3COO)2Dy(dbm)]·CH2Cl2 (2), [LZn(CH3COO)Dy(btfa)2]·CH2Cl2 (3), (H2L = N,N'-bis(3-methoxysalicylidene)-1,2-phenylenediamine, hfac = hexafluoroacetylacetone, dbm = dibenzoylmethane, btfa = benzoyltrifluoride acetone) were structurally and magnetically characterized. They have similar ZnII-DyIII structural cores bridged by N and O atoms of the hexadentate salen type ligand (L). The main difference between them is the peripheral β-diketonate co-ligands surrounding DyIII ion. Dynamic magnetic properties measurements revealed that complexes 1-3 exhibit the field-induced SMM behavior with relaxation energy barriers Ueff/kB of 45.49 K, 69.28 K and 101.34 K, respectively. The ac magnetic susceptibility of diluted sample 3Dy0.05Y0.95 confirmed the single molecule original relaxation, in which the quantum tunneling of magnetization (QTM) was suppressed efficiently and a butterfly-shaped hysteresis loop at 1.8 K was observed.

Ligand Modified and Light Switched On/Off Single-Chain Magnets of {Fe 2 Co} Coordination Polymers via Metal-to-Metal Charge Transfer

Ligand Modified and Light Switched On/Off Single-Chain Magnets of {Fe ₂ Co} Coordination Polymers via Metal-to-Metal Charge Transfer

Janus Pyrrolopyrrole Aza-dipyrrin: Hydrogen-Bonded Assemblies and Slow Magnetic Relaxation of the Cobalt(II) Complex in the Solid State.

A novel pyrrolopyrrole azadipyrrin (Janus-PPAD) with Janus duality was synthesized by a Schiff base-forming reaction of diketopyrrolopyrrole. The orthogonal interactions of the hydrogen-bonding ketopyrrole and metal-coordinating azadipyrrin moieties in Janus-PPAD enabled the metal ions to be arranged at regular intervals: zinc(II) and cobalt(II) coordination provided metal-coordinated Janus-PPAD dimers, which can subsequently form hydrogen-bonded one-dimensional arrays both in solution and in the solid state. The supramolecular assembly of the zinc(II) complex in solution was investigated by 1 H NMR spectroscopy based on the isodesmic model, in which a binding constant for the elongation of assemblies is constant. Owing to the tetrahedral coordination, in the solid state, the cobalt(II) complex exhibited a slow magnetic relaxation due to the negative D value of -27.1 cm-1 with an effective relaxation energy barrier Ueff of 38.0 cm-1 . The effect of magnetic dilution on the relaxation behavior is discussed. The relaxation mechanism at low temperature was analyzed by considering spin lattice interactions and quantum tunneling effects. The easy-axis magnetic anisotropy was confirmed, and the relevant wave functions were obtained by ab initio CASSCF calculations.

Theory of structural relaxation in glass from the thermodynamics of irreversible processes

This work proposes a fundamental thermodynamic description of structural relaxation in glasses by establishing a link between the Prony series solution to volume relaxation derived from the principles of irreversible thermodynamics and asymmetric Lévy stable distribution of relaxation rates. Additionally, it is shown that the bulk viscosity of glass, and not the shear viscosity, is the transport coefficient governing structural relaxation. We also report the distribution of relaxation times and energy barrier heights underpinning stretched exponential relaxation. It is proposed that this framework may be used for qualitative and quantitative descriptions of the relaxation kinetics in glass.

Origin of Magnetic Relaxation Barriers in a Family of Cobalt(II)-Radical Single-Chain Magnets: Density Functional Theory and Ab Initio Calculations.

Density functional theory (DFT) and ab initio calculations were performed to probe the origin of the magnetic relaxation barriers for two finite single-chain magnets (SCMs) featuring a one-dimension chain, Co(hfac)2(R-NapNIT) (R-NapNIT = 2-(2'-(R-)naphthyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, R = MeO (1) or EtO (2)). Our calculations show that the strong intrachain CoII-CoII exchange coupling interactions transmitted by radicals can contribute much more than ionic anisotropy to the height of the reversal barrier of magnetization for the single-chain magnets (SCMs) with |2E| < |4J/3|. In addition, the anisotropic energy barrier ΔA decreases with the decrease of |2E/J| ratio and finally vanishes in the limit of broad domain walls (|2E| < < |4 J/3|). Therefore, the total magnetic relaxation energy barriers of two SCMs mostly originate from the correlation energy barrier Δξ deriving from the indirect ferromagnetic interaction between CoII-CoII transmitted by the strong CoII-radical antiferromagnetic interactions.

A remarkable energy barrier for spin reversal in a field induced dinuclear ytterbium single molecule magnet.

A dinuclear ytterbium complex has been designed with a strong ligand field in equatorial positions. Magnetic studies reveal the presence of easy-axis anisotropy and field induced slow relaxation of magnetization with a remarkable energy barrier, Ueff = 53.58 cm-1, the highest value reported for any Yb-based SMMs to date. Furthermore, the ab initio calculations disclose the importance of a weak axial ligand field to design high-performance Yb-based SMMs.

Quantification of the Magnetic Anisotropy of a Single‐Molecule Magnet from the Experimental Electron Density

AbstractReported here is an entirely new application of experimental electron density (EED) in the study of magnetic anisotropy of single‐molecule magnets (SMMs). Among those SMMs based on one single transition metal, tetrahedral CoII‐complexes are prominent, and their large zero‐field splitting arises exclusively from coupling between the d and dxy orbitals. Using very low temperature single‐crystal synchrotron X‐ray diffraction data, an accurate electron density (ED) was obtained for a prototypical SMM, and the experimental d‐orbital populations were used to quantify the dxy‐d coupling, which simultaneously provides the composition of the ground‐state Kramers doublet wave function. Based on this experimentally determined wave function, an energy barrier for magnetic relaxation in the range 193–268 cm−1 was calculated, and is in full accordance with the previously published value of 230 cm−1 obtained from near‐infrared spectroscopy. These results provide the first clear and direct link between ED and molecular magnetic properties.

Quantification of the Magnetic Anisotropy of a Single-Molecule Magnet from the Experimental Electron Density.

Reported here is an entirely new application of experimental electron density (EED) in the study of magnetic anisotropy of single-molecule magnets (SMMs). Among those SMMs based on one single transition metal, tetrahedral CoII-complexes are prominent, and their large zero-field splitting arises exclusively from coupling between the d and dxy orbitals. Using very low temperature single-crystal synchrotron X-ray diffraction data, an accurate electron density (ED) was obtained for a prototypical SMM, and the experimental d-orbital populations were used to quantify the dxy-d coupling, which simultaneously provides the composition of the ground-state Kramers doublet wave function. Based on this experimentally determined wave function, an energy barrier for magnetic relaxation in the range 193-268 cm-1 was calculated, and is in full accordance with the previously published value of 230 cm-1 obtained from near-infrared spectroscopy. These results provide the first clear and direct link between ED and molecular magnetic properties.

Photoswitchable 11 nm CsCoFe Prussian Blue Analogue Nanocrystals with High Relaxation Temperature

Photoswitchable 11 nm nanocrystals with the coordination network Cs{Co[Fe(CN)6]} were obtained using a template-free method. The nanocrystals were recovered from the colloidal solutions as solid materials surrounded by cetyltrimethylammonium (CTA) cations or embedded in the organic polymer polyvinylpyrrolidone (PVP). Complementary magnetic, spectroscopic, and structural techniques, including EPR spectroscopy, reveal a majority (∼70%) of the low-spin and photoactive diamagnetic CoIIIFeII pairs located in the core of the nanocrystals and a mixture of CoIIFeII and CoIIFeIII species present mainly within the shell of the objects. While bulk compounds with similar vacancy concentration do not exhibit noticeable photoinduced charge transfer, the observed photoactivity of the nanocrystals is ascribed to their nanometric size. The relaxation temperature of the photoinduced state shifts upward by ∼55 K when PVP is replaced by CTA. This is ascribed to the larger rigidity of the dense CsCoFe_CTA material, whose metastable state is lower than that for CsCoFe_PVP, leading to a larger relaxation energy barrier and, therefore, to a higher relaxation temperature.

Chiral Photomagnets Based on Copper(II) complexes of 1,2-Diaminocyclohexane and Octacyanidomolybdate(IV) Ions.

Chiral photomagnets compose a class of multifunctional molecule-based materials with light-induced alteration of magnetization and chiral properties. The rational design and synthesis of such assemblies is a challenge, and only few such systems are known. Herein, the remarkable octacyanide-bridged enantiomeric pair of 1-D chains [Cu((R,R)-chxn)2]2[Mo(CN)8]·H2O (1R) and [Cu((S,S)-chxn)2]2[Mo(CN)8]·H2O (1S) exhibiting enantiopure structural helicity, which results in optical activity in the 350-800 nm range as confirmed by natural circular dichroism (NCD) spectra, is reported. The photomagnetic effects of 1R, 1S, and 1rac result from the blue light excitation (436 nm) of the photomagnetically active octacyanidomolybdate(IV) ions. In the excited state MoIVHS centers with S = 1 couple antiferromagnetically with the neighboring CuII centers with JCuMo values of -1.3, -1.0, and -1.1 cm-1 for 1R, 1S, and 1rac, respectively. The values of thermal relaxation energy barriers have been estimated as 142 and 356 K for 1R and 1S, being comparable with the energy range of the thermal bath. The value for 1rac reveals a significantly lower value of 75 K. On the basis of these results the value of gMoHS has been estimated to be in the range 4.8-5.8.

High-Pressure Crystallography as a Guide in the Design of Single-Molecule Magnets.

Single-molecule magnet materials owe their function to the presence of significant magnetic anisotropy, which arises from the interplay between the ligand field and spin-orbit coupling, and this is responsible for setting up an energy barrier for magnetic relaxation. Therefore, chemical control of magnetic anisotropy is a central challenge in the quest to synthesize new molecular nanomagnets with improved properties. There have been several reports of design principles targeting such control; however, these principles rely on idealized geometries, which are rarely obtained in crystal structures. Here, we present the results of high-pressure single-crystal diffraction on the single-ion magnet, Co(SPh)4(PPh4)2, in the pressure range of 0-9.2 GPa. Upon pressurization a sequence of small geometrical distortions of the central CoS4 moeity are observed, enabling a thorough analysis of the magneto-structural correlations. The magneto-structural correlations are investigated by theoretical analyses of the pressure-dependent experimental molecular structures. We observed a significant increase in the magnitude of the zero-field splitting parameter D, from -54.6 cm-1 to -89.7 cm-1, which was clearly explained from the reduction of the energy difference between the essential dxy and dx2-y2 orbitals, and structurally assigned to the change of an angle of compression of the CoS4 moeity.

Hexanuclear [Cp*Dy]6 single-molecule magnet.

A hexanuclear cluster [(Cp*Dy)6K4Cl16(THF)6], [Cp*Dy]6, has been constructed from six {Cp*DyIII} synthons in which the strongly coordinating Cp*- caps determine the local anisotropy axes. Structural characterization of [Cp*Dy]6 shows two almost parallel triangular (Cp*Dy)3 fragments that are linked by the K+ and Cl- ions. Magnetic measurements reveal slow thermal relaxation and fast quantum tunneling relaxation in the absence of an external dc field. After applying a weak dc field, the quantum tunneling relaxation is efficiently suppressed, giving a sizable energy barrier of 561 K, which represents the current record energy barrier for high nuclearity organometallic SMMs.

Different single-molecule magnets behaviors of carboxyl bridged dinuclear Dy(III) complexes induced by charged and neutral ligand

Three dinuclear dysprosium complexes, namely, Dy2(DBM)4L2(CH3CH2OH)2·2CH2Cl2(1), Dy2(DBM)4L2(CH3OH)2·2CH2Cl2(2), Dy2(BAC)4L2(CH3CH2OH)2 (3) and yttrium compound Y2(BAC)4L2(CH3CH2OH)2 (3Y) (L = 2,6-dimethoxybenzoic acid, DBM = dibenzoyl methane, BAC = Benzoylacetone), were structurally and magnetically characterized. The single-crystal structures showed that L serves as an effective bridge to link two Dy(III) centers with μ2-η1:η2-O2 coordination mode. Each Dy(III) ion was chelated by two bidentate β-diketonate co-ligands and a methanol or ethanol molecule, leading to an eight-coordinated geometry. The magnetic measurements revealed that all the complexes behaved as field-induced single-molecule magnets, and the ferromagnetic intramolecular interactions between Dy(III) ions are apparent. Strikingly, the alteration of neutral ligands between 1 and 2 did not result in a significant change of their relaxation energy barriers (Ueff/kB = 25.6 K and 26.1 K respectively), while the dramatically enhancement of energy barrier by nearly triple (91.6 K) increase was observed in 3 when modulating the terminal of β-diketonate anion and the open butterfly-shaped hysteresis loop was also observed at 1.8 K in 10% diluted samples of 3. The electrostatic model for the determination of the magnetic anisotropy in Dy complexes implemented by the Magellan program revealed that the dynamic magnetic relaxation is dominated by the charged β-diketonate ligand much more than the neutral ligand in this case.

Synthesis of a Neutral Mononuclear Four-Coordinate Co(II) Complex Having Two Halved Phthalocyanine Ligands That Shows Slow Magnetic Relaxations under Zero Static Magnetic Field.

Syntheses of a novel pseudotetrahedral four-coordinate mononuclear Co(II) complex that has two halved phthalocyanine moieties as the ligands, [Co(half-Pc)2] (1), and its magnetic properties as a single molecule magnet (SMM) are reported. A one pot reaction of phthalonitrile and lithium methoxide followed by the coordination to a Co(II) ion gave 1 as an orange solid in a moderate yield. X-ray crystallography on 1 reveals tetragonally distorted coordination geometry around the Co(II) ion. The M- HT-1 plots suggest that 1 has large axial magnetic anisotropy. The ac magnetic susceptibility data of the magnetically diluted 1 (dil.1) clearly show that the complex acts as an SMM even in the absence of the external static magnetic field ( Hdc). The influence of intermolecular and intramolecular interactions for the magnetic relaxation behaviors has been discussed by comparison of the magnetic data of 1 and dil.1. The Orbach process is suggested as the predominant mechanism of magnetic relaxations in the high-temperature range, and the Arrhenius plots provide the effective relaxation energy barrier and pre-exponential factor of Ueff = 54.0 cm-1 and τ0 = 3.17 × 10-10 s, respectively. The direct estimation of the axial anisotropic parameter of 1 was successfully performed by high-field, multifrequency ESR measurements up to 55 T and 2.5 THz. The evaluated axial zero-field splitting (ZFS) energy of 57.0 cm-1 is comparable to the Ueff energy, confirming that the magnetic relaxations are initiated by the thermal excitation from the ground | M S⟩ = |±3/2⟩ states to the |±1/2⟩ states in the high-temperature range. The results of the ab initio calculations based on the CAS(7,5) SCF wave functions indicate that the ground states of 1 consist mainly of | M S⟩ = |±3/2⟩ states, while the first excited states are the mixture of | M S⟩ = |+1/2⟩ and |-1/2⟩.

Synthesis, Structures, and Magnetic Properties of Two Coordination Assemblies of Mn(III) Single Molecule Magnets Bridged via Photochromic Diarylethene Ligands.

Two new coordination assemblies were prepared by combining the open and close forms of 1,2-bis(5-carboxyl-2-methyl-3-thienyl)perfluorocyclopentene (H2dae) with [Mn2(saltmen)2(H2O)2](PF6)2, where H2saltmen = 2,2'-((1 E,1' E)-((2,3-dimethylbutane-2,3-diyl)bis(azaneylylidene)) bis(methaneylylidene))diphenol. From X-ray diffraction analyses, the complexes had the following formula: [Mn2(saltmen)2(dae-open)] (1open) and [Mn(saltmen)(dae-close)]·H2O·Et3N (1close). Both complexes crystallized in the C2/ c monoclinic space group. In 1open, dae-o2- behaves as a bidentate ligand attached to the outer Mn-saltmen monomer via the oxygen atom of carboxylato groups, whereas in 1close, the dae-c2- ligand behaves as a monodentate ligand attached to the external Mn-saltmen dimer by only one carboxylato group of the photochromic ligand. The complexes showed reversible photochromic responses to UV/vis light and showed single-molecule magnet-like behavior. The relaxation times and energy barriers of the metal complexes are clearly affected by UV/vis irradiation.

Single‐Molecule Magnet Behavior in Two Tetranuclear Cyanide‐bridged FeIII2NiII2 Compounds

Two tetranuclear cyanide‐bridged FeIII2NiII2 compounds [Ni2(L1)4Fe2(μ‐CN)4(CN)2(L2)2]·2ClO4·CH3OH·4H2O (1) and [Ni2(L1)4Fe2(μ‐CN)4(CN)2(L3)2]·2ClO4 (2) [L1 = 4,4′‐dichloro‐2,2′‐bipyridine; L2 = hydrotris(pyrazolyl)borate; L3 = tetrakis(pyrazolyl)borate] were synthesized. Magnetic measurements indicated that both two compounds showed single‐molecule magnet (SMM) behaviors with the relaxation energy barrier of Δ/kB = 68.9(8) K for 1 and 12.6(1) K for 2. Magneto‐structural analysis indicated that the intermolecular interactions played an important part in the slow magnetic relaxation behaviors.