Influence of Emotion on Memory for Temporal Information.

Contextual information, such as color and spatial location, has been found to be better remembered for emotional than for neutral items. The current study examined whether the influence of emotion extends to memory for another fundamental feature of episodic memory: temporal information. Results from a list-discrimination paradigm showed that (a) item memory was enhanced for both negative and positive pictures compared with neutral ones and was better for negative than for positive pictures and (b) temporal information was better remembered for negative than for positive and neutral pictures, whereas positive and neutral pictures did not differ from each other. These findings are discussed in relation to the processes involved in memory for temporal information. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Carbazole based hole transporting materials for solid state dye sensitizer solar cells: role of the methoxy groups

The synthesis of new organic hole transporting materials (HTMs) based on 3,6‐disubstituted 9H‐carbazole‐3,6‐diamine,N,N,N′,N′‐tetraphenyl‐9‐(4‐methoxyphenyl) derivatives and their applications in solid state dye sensitizer solar cells (DSSCs) are described. The effect of the methoxy group localized on the para position of the diphenylamine moieties on the thermal, electronic and electrochemical properties and photovoltaic performance is discussed. In solid state DSSCs, utilization of the aforementioned HTMs in combination with the dye D102 (TiO₂/D102/HTM/Au) shows a positive influence of the methoxy group on the photovoltaic conversion efficiency compared with unsubstituted diphenylamine grafted groups. A study on the concentration of the HTM is also carried out and shows an optimal concentration around 200 mg mL^?1. Without further optimization, the best device gives a power conversion efficiency of 1.75% under AM 1.5 solar irradiation (100 mW cm^?2).     

Mastering the structure of PLA foams made with extrusion assisted by supercritical CO2

In this study, the outcome of operating conditions of extrusion assisted by supercritical CO₂ for the manufacture of poly(lactic acid) foams was investigated. It was found that the temperature before and inside the die was the most prominent parameter to tune the foam properties. Foam porosity as high as 96% could be obtained (for die temperature between 109 and 112 °C), representing a total expansion exceeding 30. In this temperature range, low crystallinity (≈6%) was induced giving foams with high radial expansion i.e., large diameters and open porosity. At 112 °C, the CO₂ was able to greatly expand the foams, providing 73% of its potential blowing effect. On the other hand, a low die temperature (below a die temperature of 107 °C) induces a significantly higher level of crystallinity resulting in foams with closed‐porosity and a large longitudinal expansion due to higher strength of the polymer melt. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45067.     

Diphenylamino-substituted derivatives of 9-phenylcarbazole as glass-forming hole-transporting materials for solid state dye sensitized solar cells

The synthesis and properties of glass-forming diphenylamino-substituted derivatives of 9-phenylcarbazole with methoxy groups in the different position of diphenylamino moieties are reported. A comparative study on their thermal, optical, photoelectrical and electrochemical properties is presented. The synthesized compounds exhibit high thermal stability with 5% weight loss temperatures ranging from 344 to 475 °C. The derivatives absorb electromagnetic irradiation in the range of 225–425 nm with the band gaps of 2.94–3.08 eV. The ionization energies of the synthesized compounds range from 5.04 to 5.56 eV. The lowest ionization energies and band gaps are observed for compounds containing para methoxy-substituted phenyl rings of diphenylamino moieties and for disubstituted carbazole derivatives. Charge-transporting properties of the selected compounds were tested by time-of-flight technique. Hole drift mobilities in the amorphous layers of the materials reach 10⁻³ cm²/V s at high electric fields. The derivatives were tested as hole transport materials in solid-state dye sensitized solar cells and showed conversion efficiency up to 0.54%.     

The effect of copolymer composition on the surface properties of perfluoroalkylethyl acrylates

The surface properties of two perfluoroalkylethyl acrylic copolymers—aqueous, Zonyl^®329 and solvent‐based, Zonyl^®225—were studied. Zonyl^®329 is a water‐based dispersion and Zonyl^®225 a solvent‐based copolymer solution; both polymers have the same perfluoroalkyethyl side chains [F(CF₂)_nCH₂CH₂? ] but have different comonomer compositions. Thin films, prepared by dip coating onto mica and quartz, with and without annealing, were characterized by contact angle and by X‐ray photoelectron spectroscopy (XPS). The contact angle measurements showed little variation with polymer and with substrate, consistent with the supposition that the perfluoroalkylethyl chains aggregate on the surface and thus dominate surface properties, irrespective of the composition of the rest of the polymer. XPS revealed only small variations in surface chemistry for studied films. Annealed films showed improved segregation for solvent‐based Zonyl^®225, which has both hydrocarbon alkyl and perfluoroalkylethyl side chains; the presence of hydrocarbon alkyl chains enables the perfluoroalkylethyl chains to reorganize after annealing. Depending on the external conditions, this thermal treatment can enable more perfluoroalkylethyl chains to reach the film surface (solid/air interface), leading to a reduction in the dispersive‐dominant surface and enhancement in perfluoroalkylethyl segregation. This suggested that perfluoroalkylethyl side chains dominate the surface properties, which are thus not dependent on substrate, backbone composition, or formulation. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Localization of human transcription factor TEF-4 and TEF-5 (TEAD2, TEAD3) genes to chromosomes 19q13.3 and 6p21.2 using fluorescence in situ hybridization and radiation hybrid analysis

The tetrapeptide Ala-lle-Gly-Met bound to a Wang resin via the methionine residue was studied by NMR under MAS conditions and compared to the same peptide in solution. The bound peptide exhibits average linewidths superior to those observed for the peptide in solution. The origin of the residual NMR linewidth observed for the bound form was investigated. The dynamics of the peptide is shown to be only marginally responsible for the increased linewidth; the major cause of the line broadening appears to be nonaveraged magnetic susceptibility differences.     

Use of BPX‐70 60‐m GC columns for screening the fatty acid composition of industrial cookies

The fatty acid (FA) composition of food is requested for labelling purposes and food composition tables. Suitable analytical methods for labelling purposes must be able to efficiently identify and accurately quantify FA as swiftly and cheaply as possible. This study evaluated a middle‐length highly polar column, the BPX‐70 60‐m column, to balance analysis efficiency and duration. The use of a 60‐m column led to the loss of data on minor FA but a gain in analysis time. The column was evaluated by analysing the FA composition of ten cookies made with different kinds of fats, including milk fat, and pure and/or partially hydrogenated vegetable oils. The FA elution order in this GC phase has been poorly documented in the literature compared to equivalent highly polar CPSil‐88 and SP‐2460 GC phases. Co‐elutions and overlaps on the BPX‐70 column were studied and commented upon. Overall, the BPX‐70 60‐m column could be used for rapid screening of the FA composition of simple foods. Analysis of the FA composition of a complex matrix, such as a dairy product, and specific analysis of trans‐FA required a longer highly polar column, possibly after fractionation by silver‐ion liquid chromatography. Compared to other GC phases, the BPX‐70 enabled effective isolation of 18:3 isomers although these isomers co‐eluted with 20:1 isomers on other highly polar GC phases. However, some CLA isomers co‐eluted with other FA on this column, and a specific analysis of these special FA would require another phase and/or different chromatographic conditions.     

Graphoepitaxy of High‐Quality GaN Layers on Graphene/6H–SiC

The implementation of graphene layers in gallium nitride (GaN) heterostructure growth can solve self‐heating problems in nitride‐based high‐power electronic and light‐emitting optoelectronic devices. In the present study, high‐quality GaN layers are grown on patterned graphene layers and 6H–SiC by metalorganic chemical vapor deposition. A periodic pattern of graphene layers is fabricated on 6H–SiC by using polymethyl methacrylate deposition and electron beam lithography, followed by etching using an Ar/O₂ gas atmosphere. Prior to GaN growth, an AlN buffer layer and an Al_0.2Ga_0.8N transition layer are deposited. The atomic structures of the interfaces between the 6H–SiC and graphene, as well as between the graphene and AlN, are studied using scanning transmission electron microscopy. Phase separation of the Al_0.2Ga_0.8N transition layer into an AlN and GaN superlattice is observed. Above the continuous graphene layers, polycrystalline defective GaN is rapidly overgrown by better quality single‐crystalline GaN from the etched regions. The lateral overgrowth of GaN results in the presence of a low density of dislocations (≈10⁹ cm⁻²) and inversion domains and the formation of a smooth GaN surface.     

Comparison of pulse subtraction Doppler and pulse inversion Doppler

In this paper, a new Doppler technique based on pulse subtraction imaging (PSD) is described and compared with pulse inversion Doppler (PID). Combining a nonlinear contrast agent imaging technique with a Doppler process provides a tool for detecting motion of both contrast agents and tissues. This has potential in targeted imaging in which attached microbubbles need to be separated from moving ones and surrounding tissues. The results from both simulation and experiment show that PSD is able to differentiate bubble motion from tissue motion. For Doppler processing conducted at the fundamental frequency, the contrast-to-tissue ratio (CTR) in PSD was 3.3 (±0.4) times higher on average than PID at a mechanical index (MI) of 0.1. At the harmonic frequency, PID was shown to have a 3.1 (±0.4) times higher CTR than PSD. Overall, taken in their optimum processing conditions, PID has a CTR up to 1.9 (±0.4) times higher than PSD. The CTRs for both techniques have also been shown to increase with increasing MI. However, for the same axial Doppler resolution. PSD also allows less energy to be transmitted into the medium, which makes it less disruptive. The relative performances of PSD and PID in terms of the bandwidth of the imaging system are also discussed.     

Involvement of surface cysteines in activity and multimer formation of thimet oligopeptidase

Thimet oligopeptidase is a metalloenzyme involved in regulatingneuropeptide processing. Three cysteine residues (246, 248,253) are known to be involved in thiol activation of the enzyme.In contrast to the wild-type enzyme, the triple mutant (C246S/C248S/C253S)displays increased activity in the absence of dithiothreitol.Dimers, purportedly formed through cysteines 246, 248 and 253,have been thought to be inactive. However, analysis of the triplemutant by native gel electrophoresis reveals the existence ofdimers and multimers, implying that oligomer formation is mediatedby other cysteines, probably on the surface, and that some ofthese forms are enzymatically active. Isolation and characterizationof iodoacetate-modified monomers and dimers of the triple mutantrevealed that, indeed, certain dimeric forms of the enzyme arestill fully active, whereas others show reduced activity. Cysteineresidues potentially involved in dimerization were identifiedby modeling of thimet oliogopeptidase to its homolog, neurolysin.Five mutants were constructed; all contained the triple mutationC246S/C248S/C253S and additional substitutions. Substitutionsat C46 or C682 and C687 prevented multimer formation and inhibiteddimer formation. The C46S mutant had enzymatic activity comparableto the parent triple mutant, whereas that of C682S/C687S wasreduced. Thus, the location of intermolecular disulfide bonds,rather than their existence per se, is relevant to activity.Dimerization close to the N-terminus is detrimental to activity,whereas dimerization near the C-terminus has little effect.Altering disulfide bond formation is a potential regulatoryfactor in the cell owing to the varying oxidation states insubcellular compartments and the different compartmental locationsand functions of the enzyme. Received March 1, 2003; revised June 17, 2003; accepted June 23, 2003.