Super-hydrophobic transparent surface by femtosecond laser micro-patterned catalyst thin film for carbon nanotube cluster growth

In this work, super-hydrophobic surfaces were fabricated by femtosecond laser micro-machining and chemical vapor deposition to constitute hybrid scale micro/nano-structures formed by carbon nanotube (CNT) clusters. Nickel thin-film microstructures, functioning as CNT growth catalyst, precisely control the distribution of the CNT clusters. To obtain minimal heat-affected zones, femtosecond laser was used to trim the nickel thin-film coating. Plasma treatment was subsequently carried out to enhance the lotus-leaf effect. The wetting property of the CNT surface is improved from hydrophilicity to super-hydrophobicity at an advancing contact angle of 161 degrees. The dynamic water drop impacting test further confirms its enhanced water-repellent property. Meanwhile, this super-hydrophobic surface exhibits excellent transparency with quartz as the substrate. This hybrid fabrication technique can achieve super-hydrophobic surfaces over a large area, which has potential applications as self-cleaning windows for vehicles, solar cells and high-rise buildings.     

Symmetry‐Guided Design and Fluorous Synthesis of a Stable and Rapidly Excreted Imaging Tracer for 19F MRI

Getting FIT : A bispherical ¹⁹F imaging tracer, ¹⁹FIT, was designed and synthesized. ¹⁹FIT is advantageous over perfluorocarbon‐based ¹⁹F imaging agents, as it is not retained in the organs and does not require complex formulation procedures. Imaging agents such as ¹⁹FIT can lead to ¹⁹F magnetic resonance imaging (MRI) playing an important role in drug therapy, analogous to the role played by ¹H MRI in disease diagnosis.

     

Lithium barium silicate,Li2BaSiO4, from synchrotron powder data

The structure of lithium barium silicate, Li₂BaSiO₄, has been determined from synchrotron radiation powder data. The title compound was synthesized by high‐temperature solid‐state reaction and crystallizes in the hexagonal space group P6₃cm. It contains two Li atoms, one Ba atom (both site symmetry ..m on special position 6c), two Si atoms [on special positions 4b (site symmetry 3..) and 2a (site symmetry 3.m)] and four O atoms (one on general position 12d, and three on special positions 6c, 4b and 2a). The basic units of the structure are (Li₆SiO₁₃)⁵⁻ units, each comprising seven tetrahedra sharing edges and vertices. These basic units are connected by sharing corners parallel to [001] and through sharing (SiO₄)⁴⁻ tetrahedra in (001). The relationship between the structures and luminescence properties of Li₂SrSiO₄, Li₂CaSiO₄ and the title compound is discussed.     

Porphyrin profiles in blood, urine and faeces by HPLC/electrospray ionization tandem mass spectrometry

A high-resolution high-performance liquid chromatography/electrospray ionization quadrupole time-of-flight tandem mass spectrometry method is described for the analysis of porphyrins in blood, urine and faeces. The gradient elution reversed-phase HPLC system using acetonitrile-methanol-1 m ammonium acetate/acetic acid buffer (pH 5.16) as gradient solvent mixtures was able to separate all porphyrin metabolites, including the type I and type III isomers of uroporphyrin, hepta-, hexa- and penta-carboxylic acid porphyrins and coproporphyrin. The porphyrins were positively identified by the protonated molecules [M+H](+) and further characterized by tandem mass spectrometric analysis with each porphyrin giving a characteristic collisioninduced dissociation product ion spectrum. The mass chromatograms obtained by HPLC/ESI MS are useful for the differential diagnosis of the porphyrias, since each type of porphyria has a typical porphyrin excretion pattern.     

On range and response: Dimensions of process flexibility

There are two dimensions to process flexibility: range versus response. Range is the extent to which a system can adapt, while response is the rate at which the system can adapt. Although both dimensions are important, the existing literature does not analytically examine the response dimension vis-a-vis the range dimension.     

Design of Gate‐Ground‐NMOS‐Based ESD Protection Circuits with Low Trigger Voltage,Low Leakage Current,and Fast Turn‐On

In this paper, electrostatic discharge (ESD) protection circuits with an advanced substrate‐triggered NMOS and a gate‐substrate‐triggered NMOS are proposed to provide low trigger voltage, low leakage current, and fast turn‐on speed. The proposed ESD protection devices are designed using 0.13 μm CMOS technology. The experimental results show that the proposed substrate‐triggered NMOS using a bipolar transistor has a low trigger voltage of 5.98 V and a fast turn‐on time of 37 ns. The proposed gate‐substrate‐triggered NMOS has a lower trigger voltage of 5.35 V and low leakage current of 80 pA.     

Development of stable phosphohistidine analogues

Protein phosphorylation is one of the most common and extensively studied posttranslational modifications (PTMs). Compared to the O-phosphorylation of Ser, Thr, and Tyr residues, our understanding of histidine phosphorylation is relatively limited, particularly in higher eukaryotes, due to technical difficulties stemming from the intrinsic instability and isomerism of phosphohistidine (pHis). We report the design and synthesis of stable and nonisomerizable pHis analogues. These pHis analogues were successfully utilized in solid-phase peptide synthesis and semi-synthesis of histone H4. Significantly, the first antibody that specifically recognizes pHis was obtained using the synthetic peptide as the immunogen.     

High-density arrays of InGaN nanorings, nanodots, and nanoarrows fabricated by a template-assisted approach

Dense, crystalline arrays of InGaN nanorings, nanodots, and nanoarrows have been fabricated on GaN substrates by template-assisted nano-area selective growth. To create the nanostructures, we have used nanoporous anodic alumina films as templates to pattern nanopores in an SiO2 transfer layer, and then used this patterned SiO2 layer as a template for nitride growth by metalorganic chemical vapor deposition. We have varied the diameter of the deposited nitride nanostructures from 35 to 250 nm by changing the initial anodic alumina template structure. In addition, by controlling the nitride growth time we have created various types of nanostructures, from nanorings to nanoarrows. This structural evolution begins with the nucleation and formation of a nanoring structure, followed by coalescence and growth to form faceted nanodots, and finally lateral overgrowth to form faceted nanoarrows.     

Conformational preferences of proline oligopeptides

A conformational study on the terminally blocked proline oligopeptides, Ac-(Pro)(n)()-NMe(2) (n = 2-5), is carried out using the ab initio Hartree-Fock level of theory with the self-consistent reaction field method in the gas phase and in solutions (chloroform, 1-propanol, and water) to explore the preference and transition between polyproline II (PPII) and polyproline I (PPI) conformations depending on the chain length, the puckering, and the solvent. The mean differences in the free energy per proline of the up-puckered conformations relative to the down-puckered conformations for both diproline and triproline increases for the PPII-like conformations and decreases for the PPI-like conformations as the solvent polarity increases. These calculated results indicate that the PPII-like structures have preferentially all-down puckerings in solutions, whereas the PPI-like structures have partially mixed puckerings. The free energy difference per proline residue between the PPII- and PPI-like structures decreases as the proline chain becomes longer in the gas phase but increases as the proline chain becomes longer in solutions and the solvent polarity increases. In particular, our calculated results indicate that each of the proline oligopeptides can exist as an ensemble of conformations with the trans and cis peptide bonds in solutions, although the PPII-like structure with all-trans peptide bonds is dominantly preferred, which is reasonably consistent with the previously observed results. In diproline Ac-(Pro)(2)-NMe(2), the rotational barrier to the cis-to-trans isomerization for the first prolyl peptide bond increases as the solvent polarity increases, whereas the rotational barrier for the second prolyl peptide bond does not show the monotonic increase as the solvent polarity increases. When the rotational barriers for these two prolyl peptide bonds were compared, it could be deduced that the conformational transition from PPI with the cis peptide bond to PPII with the trans peptide bond is initiated at the C-terminus and proceeds to the N-terminus in water. This is consistent with the results from NMR experiments on polyproline in D(2)O but opposite to the results from enzymatic hydrolysis kinetics experiments on polyproline.     

Information coverage for wireless sensor networks

Coverage is a very important issue in wireless sensor networks. Current literature defines a point to be covered if it is within the sensing radius of at least one sensor. In this paper we argue that this is a conservative definition of coverage. This definition implicitly assumes that each sensor makes a decision independent of other sensors in the field. However, sensors can cooperate to make an accurate estimation, even if any single sensor is unable to do so. We then propose a new notion of information coverage and investigate its implications for sensor deployment. Numerical and simulation results show that significant savings in terms of sensor density for complete coverage can be achieved by using our definition of information coverage compared to that by using the existing definition.