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The application of terahertz (THz) science in industrial technology and scientific research requires efficient THz detectors. Such detectors should be able to operate under various external conditions and conform to existing geometric constraints in the required application. Pyroelectric THz detectors are among the best candidates. This is due to their versatility, outstanding performance, ease of fabrication, and robustness. In this paper, we propose a compact pyroelectric detector based on a bioriented poled polyvinylidene difluoride film coated with sputtered metal electrodes for in situ absorption measurement at cryogenic temperature. The detector design was optimized for the registration system of the electron paramagnetic resonance (EPR) endstation of the Novosibirsk Free Electron Laser facility. Measurements of the detector response to pulsed THz radiation at different temperatures and electrode materials showed that the response varies with both the temperature and the type of electrode material used. The maximum signal level corresponds to the temperature range of 10–40 K, in which the pyroelectric coefficient of the PVDF film also has a maximum value. Among the three coatings studied, namely indium tin oxide (ITO), Au, and Cu/Ni, the latter has the highest increase in sensitivity at low temperature. The possibility of using the detectors for in situ absorption measurement was exemplified using two typical molecular spin systems, which exhibited a transparency of 20–30% at 76.9 cm−1 and 5 K. Such measurements, carried out directly in the cryostat with the main recording system and sample fully configured, allow precise control of the THz radiation parameters at the EPR endstation. [ABSTRACT FROM AUTHOR]

A new binuclear "paddle-wheel" complex, [Co2(bhbz)4(EtOH)2]·4EtOH (1, Hbhbz-3,5-di(tert-butyl)-4-hydroxybenzoic acid); an isostructural zinc complex (2); a and magnetically diluted sample of [Zn1.93Co0.07(bhbz)4(EtOH)2]·4EtOH (3) were obtained. Molecular structures of 1 and 2 were determined by single-crystal X-ray diffraction. DFT calculations for 1 indicate strong Co-Co antiferromagnetic exchange interactions in the binuclear fragment. It was shown that when one paramagnetic ion in the binuclear molecule is replaced by a diamagnetic zinc(II) ion, the remaining cobalt(II) ion can be considered as an isolated center with magnetic anisotropy, the parameters of which are determined by ab initio calculations. Magnetic properties for samples 1 and 3 were investigated and analyzed in detail. [ABSTRACT FROM AUTHOR]

A new 1D-coordination polymer [Co(Piv)2(NH2(CH2)6NH2)]n (1, Piv is Me3CCO2− anion) was obtained, the mononuclear fragments {Co(O2CR)2} within which are linked by μ-bridged molecules of hexamethylenediamine (NH2(CH2)6NH2). For this compound, two different monoclinic C2/c (α-1) and P2/n (β-1) phases were found at room temperature by single-crystal X-ray diffraction analysis, with a similar structure of chains and their packages in unit cells. The low-temperature phase (γ-1) of crystal 1 at 150 K corresponds to the triclinic space group P-1. As the temperature decreases, the structural phase transition (SPT) in the α-1 and β-1 crystals is accompanied by an increase in the crystal packing density caused by the rearrangements of both H-bonds and the nearest ligand environment of the cobalt atom ("octahedral CoN2O4 around the metal center at room temperature" → "pseudo-tetrahedral CoN2O2 at 150 K"). The SPT was confirmed by DSC in the temperature range 210–150 K; when heated above 220 K, anomalies in the behavior of the heat flow are observed, which may be associated with the reversibility of SPT; endo effects are observed up to 300 K. The SPT starts below 200 K. At 100 K, a mixture of phases was found in sample 1: 27% α-1 phase, 61% γ-1 phase. In addition, at 100 K, 12% of the new δ-1 phase was detected, which was identified from the diffraction pattern at 260 K upon subsequent heating: the a,b,c-parameters and unit cell volume are close to the structure parameters of γ-1, and the values of the α,β,γ-angles are significantly different. Further heating leads to a phase transition from δ-1 to α-1, which both coexist at room temperature. According to the DC magnetometry data, during cooling and heating, the χMT(T) curves for 1 form a hysteresis loop with ~110 K, in which the difference in the χMT values reaches 9%. Ab initio calculations of the electronic structure of cobalt(II) in α-1 and γ-1 have been performed. Based on the EPR data at 10 K and the ab initio calculations, the behavior of the χMT(T) curve for 1 was simulated in the temperature range of 2–150 K. It was found that 1 exhibits slow magnetic relaxation in a field of 1000 Oe. [ABSTRACT FROM AUTHOR]

Copper-nitroxide complexes are important systems in the area of molecular magnetism and are used as models for investigation of magneto-structural correlations. The complex of Cu (super 2) (super +) hexafluoroacetylacetonate (Cu (hfac) (sub 2)) with two pyrazol-substituted nitronyl nitroxides (L (super R)) represents an unusual exchange-coupled three-spin system.

The exchange coupling of spin triads is analyzed in the complexes of [Cu.sup.2+] hexafluoroacetylacetonate with two pyrazole-substituted nitronyl nitroxides. The modulation of exchange interaction between copper and nitroxides by lattice vibrations lead to the spin exchange process.

The d-group Kramers ions, having strong zero field splitting (ZFS) with axial symmetry and a negative D value for the ZFS Hamiltonian, are widely considered as candidates for use as single molecular magnets (SMMs). An important need is the means to switch the SMM between its states in a reasonably short and predictable period of time, which is generally not available. We propose an approach, Zeeman–far infrared (ZeFIR) double resonance, in which circularly polarized alternating magnetic fields in the far infrared (FIR) range induce selective magnetic dipole transitions between different Kramers doublets of the SMM and polarized microwave (mw) pulses transfer excitation inside the upper Kramers doublet. A combination of FIR and mw pulses allows unidirectional switching between +S and −S states of the ion. The proposed approach is considered for a model quartet system with total spin S = 3/2, which seems to be the most promising object for selective resonance manipulations of its states by circularly polarized radiation. [ABSTRACT FROM AUTHOR]