Acoustic-hydrophysical testing of a shallow site in coastal waters of the Korean Strait

The paper describes the results of testing experiments for solving problems of thermometry and positioning of an autonomous underwater vehicle (AUV) in the Korean Strait in a shallow sea with less than 10 m of water. The studies were conducted on acoustic tracks up to 615 m long, sensed with complex phase-shift keyed signals with a centeral frequency of 2500 Hz. Under field experiment conditions, it was shown that the resolution of the structure of pulse responses makes it possible to sense temperature changes less than one degree and to secure positioning of the AUV with an accuracy better than 1 m when operating in the near-bottom layer.     

Effect of temperature conditions of ion implantation on percolation ferromagnetism in Ge0.98Mn0.02 thin films

The effect of temperature conditions of ion implantation on the magnetic properties of Ge_0.98Mn_0.02 thin films has been studied. It has been shown that a decrease in the implantation temperature significantly increases the temperature of percolation magnetic ordering in the subsystem of dispersed Mn²⁺ ions. It has been demonstrated that the observed effect can be due to suppression of the thermally activated aggregation of Mn²⁺ ions into Ge₃Mn₅ clusters and increase in their concentration in the dispersed state.     

Slow Magnetic Relaxation,Antiferromagnetic Ordering,and Metamagnetism in MnII(H2dapsc)-FeIII(CN)6 Chain Complex with Highly Anisotropic Fe-CN-Mn Spin Coupling

Reactions of [Mn(H₂dapsc)Cl₂] ⋅ H₂O (dapsc=2,6- diacetylpyridine bis(semicarbazone)) with K₃[Fe(CN)₆] and (PPh₄)₃[Fe(CN)₆] lead to the formation of the chain polymeric complex {[Mn(H₂dapsc)][Fe(CN)₆][K(H₂O)_3.5]}_n ⋅ 1.5n H₂O ( 1 ) and the discrete pentanuclear complex {[Mn(H₂dapsc)]₃[Fe(CN)₆]₂(H₂O)₂} ⋅ 4 CH₃OH ⋅ 3.4 H₂O ( 2 ), respectively. In the crystal structure of 1 the high-spin [Mn^II(H₂dapsc)]²⁺ cations and low-spin hexacyanoferrate(III) anions are assembled into alternating heterometallic cyano-bridged chains. The K⁺ ions are located between the chains and are coordinated by oxygen atoms of the H₂dapsc ligand and water molecules. The magnetic structure of 1 is built from ferrimagnetic chains, which are antiferromagnetically coupled. The complex exhibits metamagnetism and frequency-dependent ac magnetic susceptibility, indicating single-chain magnetic behavior with a Mydosh-parameter φ=0.12 and an effective energy barrier (U_eff/k_B) of 36.0 K with τ₀=2.34×10⁻¹¹ s for the spin relaxation. Detailed theoretical analysis showed highly anisotropic intra-chain spin coupling between [Fe^III(CN)₆]³⁻ and [Mn^II(H₂dapsc)]²⁺ units resulting from orbital degeneracy and unquenched orbital momentum of [Fe^III(CN)₆]³⁻ complexes. The origin of the metamagnetic transition is discussed in terms of strong magnetic anisotropy and weak AF interchain spin coupling.     

Photochromic single-molecule magnets based on oxocarboxylate Mn<Subscript>12</Subscript> clusters and mononitrosyl Ru complexes

Mono- and dianionic oxocarboxylate Ru-Mn₁₂ clusters, [RuNO(en)₂Cl]-[Mn₁₂O₁₂(O₂CR)₁₆(H₂O)₄]₂ (R = Ph (1)), [RuNO(en)₂Cl][Mn₁₂O₁₂(O₂CR)₁₆(H₂O)₄] (R = C₆F₅ (2), CH₂Cl (3), R = CHCl₂ (4)), and [RuNO(NH₃)₄OH][Mn₁₂O₁₂(O₂CR)₁₆(H₂O)₄] (R = CH₂Cl (5), CHCl₂ (6)) containing photochromic mononitrosyl ruthenium complexes as cations were synthesized. The magnetic properties of the complexes in static and alternating magnetic fields were studied, and compounds 1–6 were found to be molecular nanomagnets. By IR spectroscopy, they were shown to exhibit also photochromic properties.     

Synthesis,structure, and NO-donor activity of the paramagnetic complex [Fe<Subscript>2</Subscript>(SC<Subscript>3</Subscript>H<Subscript>5</Subscript>N<Subscript>2</Subscript>)<Subscript>2</Subscript>(NO)<Subscript>4</Subscript>] as a model of nitrosyl [2FE-2S] proteins

The neutral dinuclear iron nitrosyl complex [Fe₂(SC₃H₅N₂)₂(NO)₄] (1) of the “g = 2.03” family with a ligand analogous to natural mercaptohistidine was synthesized by the metathesis reaction of the thiosulfate ligands in the [Fe₂(S₂O₃)₂(NO)₄]²⁻ anion with imidazolidine-2-thiolate ligands. The electrochemical determination of nitrogen oxide in solution showed that compound 1 has a lower NO-donor ability compared to the iron complexes with 1-methylimidazole-2-thiol and imidazole-2-thiol synthesized earlier. Study of the magnetic properties of polycrystals of 1 demonstrated that the effective magnetic moment at room temperature is ca. 2.45 μ_B and corresponds to a molecule containing a pair of the noninteracting spins S = 1/2. This is evidence that each iron coordination unit in complex 1 contains one unpaired electron, and the iron atom is in the low-spin state. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 28–34, January, 2007.