Publications by authors named "Sang Ho Lim"

We report the ability to trap the dimer Au(μ-dppe)I (dppe is 1,2-bis(diphenylphosphino)ethane) with different separations between the three-coordinate gold ions in crystalline solvates. All of these solvates ((Au(μ-dppe)I·4(CHCl) (), Au(μ-dppe)I·2(CHCl) (), the polymorphs α-Au(μ-dppe)I·2(HC(O)NMe) () and β-Au(μ-dppe)I·2(HC(O)NMe) (), and Au(μ-dppe)I·4(CHCl) ()) along with polymeric {Au(μ-dppe)I}·(CHCl) ()) originated from the same reaction, only the solvent system used for crystallization differed. In the different solvates of Au(μ-dppe)I, the Au···Au separation varied from 3.

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To efficiently degrade organic pollutants, photocatalysts must be effective under both ultraviolet (UV) radiation and sunlight. We synthesized a series of new metal-organic frameworks by using mild hydrothermal conditions. These frameworks incorporate three distinct bipyridyl ligands: pyrazine (pyr), 4,4'-bipyridine (bpy), and 1,2-bis(4-pyridyl)ethane (bpe).

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A spontaneous crystallization of an uranium(VI)-organic coordination compound with sodium and 2-methoxybenzoate (2-mba) was observed in acidic solutions, and the solubility product, molecular vibrations, crystal structure, thermal stability, and emission properties of the atypically low-soluble U(VI) complex (Na[UO(2-mba)]·12HO(s)) were fully investigated for the first time. A long-term solubility experiment and speciation modeling gave a solubility product of log = -12.18 ± 0.

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We report the magnetic phase transitions of a spin-5/2, 2-dimensional triangular lattice antiferromagnet (AFM) NaBaMn(PO). From specific heat measurements, we observe two magnetic transitions at temperatures 1.15 and 1.

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Environmental damage from serious nuclear accidents should be urgently restored, which needs the removal of radioactive species. Radioactive iodine isotopes are particularly problematic for human health because they are released in large amounts and retain radioactivity for a substantial time. Herein, we prepare platinum-coated iron nanoparticles (Fe@Pt) as a highly selective and reusable adsorbent for iodine species, i.

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Complexation of actinides and lanthanides with carboxylic organic ligands is a critical issue affecting radionuclide migration from deep geological disposal systems of spent nuclear fuel. A series of Eu(iii)-aliphatic dicarboxylate compounds, as chemical analogs of radioactive Am(iii) species, Eu(Ox)(HO), Eu(Mal)(HO), and Eu(Suc)(HO), were synthesized and characterized using X-ray crystallography and time-resolved laser fluorescence spectroscopy to examine the ligand-dependent binding modes and the corresponding changes in spectroscopic properties. Powder X-ray crystallography results confirmed that all of the compounds presented a crystalline polymer structure with a trigonal prism square-face tricapped polyhedron geometry centered on Eu(iii) in a nine-coordinate environment involving nine oxygen atoms.

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We provide the material synthesis method, crystal structure information, and characterization of a novel mixed-valent metal oxide KInTeTeO, closely related to zirconolite (CaZrTiO), a radioactive waste immobilized material, having a 3D framework. The reported metal oxide containing an alkali-metal cation (K), main-group cation (In), tellurate, and tellurite has been synthesized as both single crystals and a pure polycrystalline phase through a hydrothermal synthesis method. Single-crystal X-ray diffraction indicates that KInTeO crystallizing in the orthorhombic space group (No.

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The magnetic and interface properties of [Pt/Co/Pt] were investigated. First, the magnetic properties were determined from the magnetic dead layer plots, in which the Co layer was considered as two distinct parts representing different magnetic properties. The two parts with low and high t ranges are close to and away from the top interface (Co/Pt), respectively.

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The coverage and temperature dependence of ZIRLO cladding with HO adsorption are studied using synchrotron-based high-resolution photoemission spectroscopy (HRPES). Based on the analytical results of the Zr 3d, O 1 s, C 1 s, and Sn 3d HRPES profiles prior to HO adsorption, we determine the surface compositions of O, hydroxyl OH, chemisorbed HO, zirconium carbide, adventitious carbon, Sn metal, and SnO in ZIRLO. When ZIRLO is exposed to HO molecules, the relative proportion of zirconium metal decreases, whereas that of the total zirconium oxides increases, suggesting the reaction between HO and the zirconium metal in ZIRLO.

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The low-field sensitivity of a giant magnetoresistance (GMR) spin valve can be enhanced by tailoring the bias field of the free layer because this sensitivity and bias field are known to show a strong correlation. In this study, the free-layer bias field is reduced considerably to almost zero via the insertion of an ultrathin nonmagnetic spacer between the pinned layer and the pinning layer. The spacer promotes an increase in the density of Néel walls in the pinned layer.

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The mono- and di-chloroform solvates of [Au (μ-1,2-bis(diphenylarsino)ethane) ](AsF ) undergo single-crystal-to-single-crystal transformations that result in gain (over 12 hours) or slow loss (over five years) of only one chloroform molecule. The change in solvation results in changes in the structure and luminescence of the digold cation. The cation consists of a pair of slightly bent As-Au-As units that are connected through the two bridging dpae ligands and by aurophilic interactions with Au⋅⋅⋅Au contacts of 3.

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The perpendicular magnetic anisotropy (PMA) properties of Pt/Co/MgO trilayers are investigated as a function of the MgO sputtering power (P) and its thickness (t), both of which are important parameters affecting the degree of oxygen interpenetration into Co during sputtering. A strong PMA is achieved at small values of P and t, where the oxygen interpenetration into Co is expected to be small. The range of oxygen interpenetration is relatively extended in such a way that it affects both the Pt/Co and Co/MgO interfaces.

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In this study, we derive analytical expressions for the critical switching current density induced by spin Hall effect in magnetic structures with the first- and second-order perpendicular magnetic anisotropy. We confirm the validity of the expressions by comparing the analytical results with those obtained from a macrospin simulation. Moreover, we find that for a particular thermal stability parameter, the switching current density can be minimized for a slightly positive second-order perpendicular magnetic anisotropy and the minimum switching current density can further be tuned using an external magnetic field.

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A large change is observed in the magnetic properties of amorphous Fe-Zr thin films sputtered at different Ar pressures. The change depends on the composition of the alloys and at compositions near 60 at.% Fe, for example, the magnetisation measured at 10 kOe increases 30-fold with an increase in the Ar pressure from 2 to 10 mTorr.

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Left ventricular aneurysm (LVA) and false aneurysm are complications of acute myocardial infarction, trauma, and cardiac surgery. Left ventricular false aneurysm (LVFA) is a particularly catastrophic complication owing to its high propensity for rupture. Surgical resection should be considered for LVFA occurring within three months after myocardial infarction or development of congestive heart failure.

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Background: The development of single-port thoracoscopic surgery and two-lung ventilation reduced the invasiveness of minor thoracic surgery. This study aimed to evaluate the feasibility and safety of single-port thoracoscopic bleb resection for primary spontaneous pneumothorax using two-lung ventilation with carbon dioxide insufflation.

Methods: Between February 2009 and May 2014, 130 patients underwent single-port thoracoscopic bleb resection under two-lung ventilation with carbon dioxide insufflation.

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Artificial interface anisotropy is demonstrated in alternating Co/Pt and Co/Pd stripe patterns, providing a means of forming magnetic anisotropy using lithography. In-plane hysteresis loops measured along two principal directions are explained in depth by two competing shape and interface anisotropies, thus confirming the formation of interface anisotropy at the Co/Pt and Co/Pd interfaces of the stripe patterns. The measured interface anisotropy energies, which are in the range of 0.

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Massive air leakage through a lacerated lung produces inadequate ventilation and hypoxemia. Tube exchange from a single to double lumen endotracheal tube (DLT), and lung separation to maintain oxygenation, are challenging for seriously injured patients. In this case report, we aim to describe how a bronchial blocker (BB) makes it easier to perform a lung separation in this situation; it also increases the overall safety of the procedure.

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Objectives: One-lung ventilation is considered to be mandatory in video-assisted thoracoscopic surgery. However, the authors showed in a previous report that two-lung ventilation with low tidal volume is feasible in thoracoscopic bleb resection (TBR). In this study, they evaluated optimal respiratory rate during TBR under two-lung ventilation with low-tidal volume anesthesia.

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The colorless, two-coordinate gold(i) complex, [(H2O)3Na][Au(SCSN3)2], has been synthesized through the [2 + 3] cyclic reaction of carbon disulfide and sodium azide in the presence of the labile complex (tht)AuCl. Metathesis of [(H2O)3Na][Au(SCSN3)2], with tetra(phenyl)arsonium chloride produced colorless needles of (Ph4As)[Au(SCSN3)2]. The structure of [(H2O)3Na][Au(SCSN3)2] involves linear gold coordination by two exocyclic sulfur atoms of the 1,2,3,4-thiatriazole-5-thiolate anions.

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1,3,5-Tris(4-phosphonophenyl)benzene was synthesized via a microwave heating assisted route and was subsequently used for the preparation of a new zirconium phosphonate with honeycomb-like structure displaying remarkable thermal stability and hydrolysis resistance.

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Follicular helper T (TFH) cells are recently highlighted as their crucial role for humoral immunity to infection as well as their abnormal control to induce autoimmune disease. During an infection, naïve T cells are differentiating into TFH cells which mediate memory B cells and long-lived plasma cells in germinal center (GC). TFH cells are characterized by their expression of master regulator, Bcl-6, and chemokine receptor, CXCR5, which are essential for the migration of T cells into the B cell follicle.

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Background: Sevoflurane anesthesia commonly causes emergence agitation (EA) in children. One previous study has reported that the use of nitrous oxide (N2O) during the washout of sevoflurane may reduce EA by decreasing the residual sevoflurane concentration, while many animal studies suggest that N2O poses a potential risk to children. The present study was designed to compare EA in children assigned to receive sevoflurane with N2O (group N) or sevoflurane alone (group S).

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In this study, the thermal stability and critical switching field of nanostructured elliptical synthetic ferrimagnets are calculated by using an analytical/numerical combined method, and the relationship between the two parameters is investigated. In conventional single magnetic layers, the critical switching field is a good measure of the thermal stability since the anisotropy, which determines the thermal stability, scales with the critical switching field. However, no such correlation is expected in nanostructured synthetic ferrimagnets, where the anisotropy is poorly defined owing to the strong interlayer magnetostatic interactions between two magnetic layers.

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An array of coordination-driven supramolecular metal-ligand clusters has been synthesized using polytopic phosphine ligands and coinage metals (Cu(+), Ag(+), Au(+)). Rigid 3-fold or 2-fold symmetric phosphine ligands have been prepared: 1,3,5-tris((4-(diphenylphosphino)ethynyl)phenyl)benzene) (tppepb, L(1)), 1,4-bis((diphenylphosphino)ethynyl)benzene (1,4-dppeb, L(2)), 1,3-bis((diphenylphosphino)ethynyl)benzene (1,3-dppeb, L(3)), 2,6-bis((diphenylphosphino)ethynyl)pyridine (2,6-dppep, L(4)), and 1,5-bis((diphenylphosphino)ethynyl)naphthalene (1,5-dppen, L(5)). Self-assembly of these ligands with coinage metals produces four different types of metal-ligand clusters, or in some cases coordination polymers, depending on number and relative geometry of the phosphine donor atoms.

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