Some Conditions on Real Hypersurfaces in Quaternionic Projective Spaces in Terms of Lie Derivatives

The purpose of this paper is to give a non-existence property with the Lie derivative of the structure tensors φ _i and some characterizations of real hypersurfaces of type A ₁, A ₂ in a quaternionic projective space QP ^m in terms of the Lie derivatives of the second fundamental tensor A and the induced Riemannian metric g on the distribution D ^⊥ = Span {U ₂, U ₂, U ₃}. This revised version was published online in June 2006 with corrections to the Cover Date.     

On the short carbonyl bond in bis[μ‐1,2‐benzisothiazol‐3(2H)‐one 1,1‐dioxido‐κ2N:O]bis{[1,2‐benzisothiazol‐3(2H)‐one 1,1‐dioxido‐κN]bis(imidazole)copper(II)}

The short carbonyl bond in the title compound, [Cu₂(C₇H₄­NO₃S)₄(C₃H₄N₂)₄] [Liu, Huang, Li & Lin (1991). Acta Cryst. C 47 , 41–43], is an artifact of disorder in the iso­thia­zol‐3(2H)‐one 1,1‐dioxide part of the 1,2‐benziso­thia­zol‐3(2H)‐one entity. In the present redetermination, all bond dimensions in the centrosymmetric dinuclear mol­ecule are normal. The five‐coordinate Cu atom shows trigonal–bipyramidal coordination. Hydro­gen bonds from the imidazole donor ligand link adjacent mol­ecules into a two‐dimensional layer structure.     

Comparison of Operating Mechanisms for the Poly(N-vinylcarbazole) Based Non-Volatile Memory Devices

Summary: The organic non-volatile memory devices (NVMs) based on poly(N-vinylcarbazole) (PVK) with the different structures and compositions were fabricated and evaluated. The resistance states in the devices were controlled by the external electric field and exhibited the distinctive properties; the device with a single PVK layer was a write-once read-many-times memory by the field induced filament as a conduction path and its memory properties depended on the PVK thickness, the PVK/Al/PVK structured device was operated by a space charge limited current model and was sensitive to preparing condition of the internal Al layer, and the device performances with the PVK based charge transfer complex depended on the composition of the CT materials and the surface condition of the bottom electrode.     

Experimental and numerical analysis of spray-atomization characteristics of biodiesel fuel in various fuel and ambient temperatures conditions

The purpose of this work is to reveal the effects of fuel temperatures and ambient gas conditions on the spray-atomization behavior of soybean oil methyl ester (SME) fuel. The spray-atomization behavior was analyzed through spray parameters such as the axial distance from the nozzle tip, local and overall Sauter mean diameter (SMD). These parameters were obtained from a spray visualization system and a droplet measuring system. In addition, the experimental results were compared with the numerical results calculated by the KIVA-3V code. It was revealed that the increase of the fuel temperature (from 300 K to 360 K) little affects the spray liquid tip penetration. The increase of the ambient gas temperature (from 300 K to 450 K) caused a increase in the spray liquid tip penetration. Also, biodiesel fuel evaporation actively occurred due to the increase in the fuel temperature and the ambient gas temperature. Of special significance was that the highest vapor fuel mass concentration was observed at the center region of the spray axis. In the results of the microscopic characteristics, the detected local droplet size at the axial direction and overall droplet size at the axial and radial direction in a control volume increased when the fuel temperature increased. This is believed to be due to an increase in the number of small droplets that quickly evaporated. In addition, the increased fuel temperature caused the decrease of the number of droplets and the increase of the vapor fuel mass. The mean axial velocity of droplets decreased with increasing fuel temperature.     

Gold Nanostructures Formed in Ionic Clusters of Perfluorinated Ionomer

Summary: Gold nanoparticles and nanorods have been synthesized in the ionic cluster network of Nafion using a liquid‐phase chemical impregnation/reduction process seemingly visualizing the phase‐separated hydrated cluster network of Nafion. The spherical shape of the hydrated clusters is clearly seen by the replicated gold nanoparticles with diameters of 5–6 nm. The gold nanoparticles grow through the Nafion cluster network to form gold nanorods with diameters of 5–6 nm and a characteristic length of 12–15 nm, which compare well to the previously reported small‐angle X‐ray scattering results. Tiny channels between adjacent spherical clusters are also observed, which expand to form a rod structure by a reorganization of ion exchange sites and an elastic deformation of Nafion polymer chains. The gold nanorods become interconnected in a cascadic feature, and a tripod‐shaped nanorod structure is one of the most commonly observed structures of the replicated gold. Although further study should be performed, the synthesized gold may be used to visualize the hydrated cluster and the network structure of Nafion, which could be used as important information in identifying the morphology and ion transport phenomena of Nafion.

Gold nanoparticles and nanorods growing through a hydrated Nafion cluster network.     

Comparative analysis of characteristics of Si, Mg, and undoped GaN

We have grown undoped, Si- and Mg-doped GaN epilayers using metalorganic chemical vapor deposition. The grown samples have electron Hall mobilities (carrier concentrations) of 798 cm²/V s (7×10¹⁶ cm⁻³) for undoped GaN and 287 cm²/V s (2.2×10¹⁸ cm⁻³) for Si-doped GaN. Mg-doped GaN shows a high hole concentration of 8×10¹⁷ cm⁻³ and a low resistivity of 0.8 Ω cm. When compared with undoped GaN, Si and Mg dopings increase the threading dislocation density in GaN films by one order and two orders, respectively. Besides, it was observed that the Mg doping causes an additional biaxial compressive stress of 0.095 GPa compared with both undoped and Si-doped GaN layers, which is due to the incorporation of large amount of Mg atoms (4–5×10¹⁹ cm⁻³).     

Size-selective shell cross-linked interior functionalized siloxane nanocages

A new structure, consisting of a shell cross-linked, 2 nm size siloxane nanocage containing propylamine groups tethered to the interior face of the shell was synthesized, starting with micelles of the surfactant molecule, (triethoxysilyl)propylcetylcarbamate. After hydrolysis of the ethoxysilyl groups and condensation and capping of the silanols to form a cross-linked, one-atom-layer-thick siloxane shell, the carbamate was converted to amine, releasing the cetyl group from the structure and resulting in the desired spherical nanocage. The intermediates in the synthesis process and the final structure were characterized by 1H and 29Si NMR, DLS, TEM, and mass spectroscopy. The amine groups tethered to the interior surface of the shell react readily with ninhydrin but do not interact with the larger ZnTPP, indicating molecular size selectivity by the cross-linked shell. The structure also exhibits confinement effect in the amine-catalyzed decarboxylation of acetoacetic acid, exhibiting higher activity and higher selectivity for acetal than (aminopropyl)triethoxysilane.     

Steric control of a bridging ligand for high-nuclearity metallamacrocycle formation: a highly puckered 60-membered icosanuclear metalladiazamacrocycle

A novel S4-symmetric icosanuclear manganese metalladiazamacrocycle was synthesized using a pentadentate ligand, N-3-phenyl-trans-2-propenoylsalicylhydrazide (H3L), that has a rigid and bulky terminal N-acyl group. A 20 cyclic repeat of an--(Mn-N-N)--linkage resulted in a highly puckered diaza-bridged 60-membered icosanuclear metallamacrocycle. The steric interaction between the ligands in the cyclic system leads to five consecutive Mn(III) centers in a chemically different--(Mn(A)Mn(B)Mn(C)Mn(D)Mn(E))--environment, with the chiralities of the metal centers being in a rather complicated--(LambdaLambdaDeltaLambdaLambda)(DeltaDeltaLambdaDeltaDelta)--sequence.