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Qubits are the basic unit of quantum information and computation. To realize quantum computing and information processing, the decoherence times of qubits must be long enough. Among the studies of molecule‐based electron spin qubits, most of the work focused on the ions with the spin S=1/2, where only single‐bit gates can be constructed. However, quantum operations require the qubits to interact with each other, so people gradually carry out relevant research in ions or systems with S>1/2 and multilevel states. In this work, a two‐dimensional (2D) oxygen‐coordinated GdIIINaI‐based oxamato supramolecular coordination framework, Na[Gd(4‐HOpa)4(H2O)] ⋅ 2H2O (1, 4‐HOpa=N‐4‐hydroxyphenyloxamate), was selected as a possible carrier of qubit. The field‐induced slow magnetic relaxation shows this system has phonon bottleneck (PB) effect at low temperatures with a very weak magnetic anisotropy. The pulse electron paramagnetic resonance studies show the spin‐lattice and spin‐spin relaxation times are T1=1.66 ms at 4 K and Tm=4.25 μs at 8 K for its diamagnetically diluted sample (1Gd0.12 %). It suggested that the relatively long decoherence time is mainly ascribed to its near isotropic and the PB effect from resonance phonon trapped for pure sample, while the dilution further improves its qubit performance. [ABSTRACT FROM AUTHOR]

Two seven-coordinate Co(II)-nitrate complexes, [Co(tmpdc)(NO3)2] (1) and [Co(tmpdt)(NO3)2]·CH3CN (2) (tmpdc = N,N,N′,N′-tetramethyl-2,6-pyridinedicarboxamide, tmpdt = N,N,N′,N′-tetramethyl-2,6-pyridinedithiocarboxamide) with tridentate neutral ligands tmpdc or tmpdt have been prepared. Their crystal structures by single X-ray diffraction show markedly different coordination geometries when two donor atoms of the tridentate ligand change from oxygen in 1 to sulfur in 2. Complex 1 is a capped octahedral while complex 2 is a pentagonal bipyramid. Results of direct-current (dc) magnetic measurements and high-frequency electron paramagnetic resonance (HFEPR) indicate the anisotropic S = 3/2 spin ground state of the Co(II) ions with the easy-plane anisotropy for both 1 and 2. Frequency- and temperature-dependent alternating-current (ac) magnetic susceptibility studies reveal slow magnetic relaxation for 1 and 2 under applied fields. [ABSTRACT FROM AUTHOR]

The polycrystals of S = 1/2 spin-dimer compound BaCu(SeO 3) 2 have been synthesized by using solid-state reaction. Without long-range order, the magnetic susceptibility χ (T) curve presents two anomalies at T 1 = 5 K and T G = 58 K due to antiferromagnetic (AFM) short-range order and short-range ferromagnetic (FM) correlations, respectively, which is further supported by the specific heat and electron spin resonance data. The high-temperature χ (T) curve follows the Curie-Weiss law with θ CW = 11.3 K, showing the dominant intradimer FM interaction. The magnetization M (H) curve at 2 K is characteristic of an AFM-FM transition at 0.4 T, suggesting the weak interdimer AFM couplings. The density function theory calculations and quantum Monte Carlo simulations allow an estimation of the intradimer and interdimer exchanges with J 1 / k B = 39.09 K, J 2 / k B = −1.51 K, and J 3 / k B = −1.68 K. Interestingly, the χ −1(T) curve within θ CW < T < T G deviates downward from paramagnetic Curie-Weiss behavior, mimicking the Griffiths-like phase. This is further supported by the ac magnetic susceptibility and magnetic relaxation measurements. The competing intradimer FM and interdimer AFM exchanges with a subtle ratio between them are proposed to be responsible for the formation of Griffiths-like phase. [Display omitted] • Spin-dimer compound BaCu 2 (SeO 3) 2 has been successfully synthesized. • The χ −1(T) curve within θ CW < T < T G deviates downward from PM Curie-Weiss behavior, mimicking the Griffiths-like phase. • The DFT calculations show that the intradimer interaction is FM with J 1 / k B = 39.09 K, the interdimer couplings are weak. • The magnetization reaches 1.06 μ B /Cu2+ at 30 T, very close to the saturated value of 1.08 μ B /Cu2+ (g = 2.15 from ESR). [ABSTRACT FROM AUTHOR]

Two air-stable Co(III)–Co(II) mixed-valence complexes of molecular formulas [CoIICoIII(L)(DMAP)3(CH3COO)]·H2O·CH3OH (1) and [CoIICoIII(L)(4-Pyrrol)3 (CH3COO)]·0.5CH2Cl2 (2) (H4L = 1,3-bis-(5-methyl pyrazole-3-carboxamide) propane; DMAP = 4-dimethylaminopyridine; and 4-Pyrrol = 4-pyrrolidinopyridine) were synthesized and characterized by single-crystal X-ray crystallography, high-field electron paramagnetic resonance (HFEPR) spectroscopy, and magnetic measurements. Both complexes possess one five-coordinated paramagnetic Co(II) ion and one six-coordinated Co(III) ion with octahedral geometry. Direct-current magnetic susceptibility and magnetization measurements show the easy-axis magnetic anisotropy that is also confirmed by low-temperature HFEPR measurements and theoretical calculations. Frequency- and temperature-dependent alternating-current magnetic susceptibility measurements reveal their field-assisted slow magnetic relaxation, which is a characteristic behavior of single-molecule magnets (SMMs), caused by the individual Co(II) ion. The effective energy barrier of complex 1 (49.2 cm−1) is significantly higher than those of the other dinuclear Co(III)–Co(II) SMMs. This work hence presents the first instance of the dinuclear Co(III)–Co(II) single-molecule magnets with a five-coordinated environment around the Co(II) ion. [ABSTRACT FROM AUTHOR]

• A soft tripodal ligand was used to construct a high-spin Co(II) complex with weak ligand field. • HFEPR and magnetic data reveal easy-axis anisotropy and SMM's behavior for this complex. • This complex is the first instance of Co(II)-based single-ion magnet with an octahedral CoS 6 unit. The soft donor ligands are of great importance to the pursuit of 3d transition-metal complexes with large magnetic anisotropy. Herein, a soft tripodal ligand, hydrotris(mercaptobenzothiazolyl)borate (Tbz) was used to construct a high-spin mononuclear complex [CoII(Tbz) 2 ] (1), having an octahedral geometry in an S 6 donor set. The combination of direct-current (dc) magnetic susceptibility and Low-temperature high-field electron paramagnetic resonance (HFEPR) reveals the easy-axis magnetic anisotropy of 1. Complex 1 shows field-induced slow relaxation of magnetization at an applied magnetic field of 1000 Oe, indicating the behavior of single-molecule magnet. The foregoing result constitutes the first instance of Co(II)-based single-ion magnet containing a CoS 6 unit. [ABSTRACT FROM AUTHOR]

• The magnetic decoupling between the Cu1 ferromagnetic chain and the Cu2 antiferromagnetic chain has been revealed. • The high-field magnetization presents a metamagnetic transition at 1.7 T and a half-saturated ferromagnetic (FM)-like magnetization process. • The antiferromagnetic resonances of the antiferromagnetically coupled Cu1 FM chains were observed, showing the presence of significant magnetic anisotropy. The high-field magnetization and electron spin resonance (ESR) are reported for the two-dimensional triangular-lattice antiferromagnet Cu 2 (OH) 3 HCO 2. The compound has an antiferromagnetic (AFM) order at T N = 4.9 K with the Curie-Weiss temperature θ CW = − 3.8 K. The high-field magnetization up to 50 T exhibits a metamagnetic transition at 1.7 T followed by a half-saturated ferromagnetic (FM)-like magnetization process, showing the magnetic decoupling between the Cu1 FM chain and the Cu2 AFM chain. The unsaturated magnetization at 50 T serves as an evidence of much larger AFM exchange in the Cu2 chain. The temperature-dependent ESR spectra are in line with the development of magnetic correlations and AFM ordering. The observed ESR modes below T N originate from the AFM resonances of the antiferromagnetically coupled Cu1 FM chains. The zero-field gap of 111 GHz and the zero-frequency field of 2.4 T suggest the presence of significant magnetic anisotropy. [ABSTRACT FROM AUTHOR]