Synthesis and characterization of MDI-butanediol urethane model compounds

Hard-segment model compounds containing one to five 4,4′-methylene bis(p-phenylisocyanate) (MDI) units extended with 1,4-butanediol (BD) were synthesized. The ends of the model compounds were reacted with ethanol. The melting point (T_m) of the model compounds increased with the number of MDI units to an extrapolated value of 299°C for the homopolymer using Flory's equation accounting for chain end defects. The ΔH of fusion was 5.3 kcal/mol. Intrinsic viscosity measurements in DMA solutions revealed a Mark Houwink exponent of 1.43 suggesting that the hard-segment model compounds are rodlike in solution. Wide-angle X-ray diffraction showed that the percentage of hard-segment crystallinity decreased as the oligomer length increased. Infrared spectroscopy studies showed that the distribution of hydrogen bond distances between C?O and NH groups became broader with increasing segment length.     

Micromachined high frequency PMN-PT/epoxy 1-3 composite ultrasonic annular array

This paper reports the design, fabrication, and performance of miniature micromachined high frequency PMN-PT/epoxy 1-3 composite ultrasonic annular arrays. The PMN-PT single crystal 1-3 composites were made with micromachining techniques. The area of a single crystal pillar was 9 × 9 μm. The width of the kerf among pillars was ∼5 μm and the kerfs were filled with a polymer. The composite thickness was 25 μm. A six-element annular transducer of equal element area of 0.2 mm² with 16 μm kerf widths between annuli was produced. The aperture size the array transducer is about 1.5 mm in diameter. A novel electrical interconnection strategy for high density array elements was implemented. After the transducer was attached to the electric connection board and packaged, the array transducer was tested in a pulse/echo arrangement, whereby the center frequency, bandwidth, two-way insertion loss (IL), and cross talk between adjacent elements were measured for each annulus. The center frequency was 50 MHz and −6 dB bandwidth was 90%. The average insertion loss was 19.5 dB at 50 MHz and the crosstalk between adjacent elements was about −35 dB. The micromachining techniques described in this paper are promising for the fabrication of other types of high frequency transducers, e.g. 1D and 2D arrays.     

Analysis of effect of casein phosphopeptides on zinc binding using mass spectrometry

Phosphorylation is one of the key events in signal transduction and zinc plays an important catalytic and/or structural role in many biological systems. The binding of Zn to a phosphopeptide will alter the physiological functions of a peptide. The binding of casein phosphopeptides (CPPs) to Zn has been analyzed using nanospray mass spectrometry. Electrospray ionization (ESI) spectra of peptides produced by tryptic digestion of alpha-casein incubated with Zn show both free and Zn-bound phosphopeptides. The interaction of CPPs and the corresponding dephosphorylated peptides with zinc is compared. This study demonstrates that the phosphorylation state of a peptide dramatically affects Zn binding, with the decrease in Zn-bound forms of peptide paralleling the decrease in phosphorylation as casein is chemically dephosphorylated, although, in some cases, a small amount of residual Zn-binding capacity remains in the completely dephosphorylated peptide. The observed fragmentation patterns of the Zn-bound CPPs support the thesis that nonphosphorylated residues are involved in the metal binding.     

Improving the performance of self-organizing maps via growing representations

Self-organizing maps (SOMs) are a type of artificial neural network that through training can produce simplified representations of large, high dimensional data sets. These representations are typically used for visualization, classification, and clustering and have been successfully applied to a variety of problems in the pharmaceutical and bioinformatics domains. SOMs in these domains have generally been restricted to static sets of nodes connected in either a grid or hexagonal connectivity and planar or toroidal topologies. We investigate the impact of connectivity and topology on SOM performance, and experiments were performed on fixed and growing SOMs. Three synthetic and two relevant data sets from the chemistry domain were used for evaluation, and performance was assessed on the basis of topological and quantization errors after equivalent training periods. Although we found that all SOMs were roughly comparable at quantizing a data space, there was wide variation in the ability to capture its underlying structure, and growing SOMs consistently outperformed their static counterparts in regards to topological errors. Additionally, one growing SOM, the Neural Gas, was found to be far more capable of capturing details of a target data space, finding lower dimensional relationships hidden within higher dimensional representations.     

A fulleropyrrolidine end-capped platinum-acetylide triad: the mechanism of photoinduced charge transfer in organometallic photovoltaic cells

The fullerene end-capped platinum acetylide donor-acceptor triad Pt(2)ThC(60) was synthesized and characterized by using photophysical methods and photovoltaic device testing. The triad consists of the platinum acetylide oligomer Ph-[triple bond, length as m-dash]-Pt(PBu3)2-[triple bond, length as m-dash]-Th-[triple bond, length as m-dash]-Pt(PBu3)2-[triple bond, length as m-dash]-Ph (Ph=phenyl and Th=2,5-thienyl, stereochemistry at both Pt centers is trans) that contains fulleropyrrolidine moieties on each of the terminal phenylene units. Electrochemistry of the triad reveals relatively low potential oxidation and reduction waves corresponding, respectively, to oxidation of the platinum acetylide and reduction of the fulleropyrrolidine units. Photoluminescence spectroscopy shows that the singlet and triplet states of the platinum acetylide chromophore are strongly quenched in the triad assembly, both in solution at ambient temperature as well as in a low-temperature solvent glass. The excited state quenching arises due to intramolecular photoinduced electron transfer to produce a charge separated state based on charge transfer from the platinum acetylide (donor) to the fulleropyrrolidine (acceptor). Picosecond time resolved absorption spectroscopy confirms that the charge transfer state is produced within 1 ps of photoexcitation, and it decays by charge recombination within 400 ps. Organic photovoltaic devices fabricated using spin-coated films of Pt2ThC60 as the active material operate with modest efficiency, exhibiting a short circuit photocurrent of 0.51 mA cm(-2) and an open circuit voltage of 0.41 V under 100 mW cm(-2)/AM1.5 illumination. The results are discussed in terms of the relationship between the mechanism of photoinduced electron transfer in the triad and the comparatively efficient photovoltaic response exhibited by the material.