Thermostable polymers and, more particularly, thermostable fibers and films are becoming more and more important as the demands of space-age technology increase. In the preparation of thermostable fibers having good tensile strengths and practical utility the processibility of the polymer is of great importance. Aromatic polyamides meet the two most important requirements: a high degree of thermal stability and an ease of preparation as viscous solutions that can be spun into fibers or cast into films. 相似文献
A convenient method for oxidative decarboxylation of α-amino acids is presented. The aldehyde products may be isolated or converted to tetrahydroisoquinolines by addition of dopamine via Pictet–Spengler reaction. Racemic products are generated by phosphate buffer >300 mM to maximize regioselectivity. (S)-Enantiomer products are generated by norcoclaurine synthase reaction in maleic acid buffer to minimize chemical background reaction. 相似文献
Desirable components for dye‐sensitzed solar cell (DSC) sensitizers and fluorescent imaging dyes include strong donating building blocks coupled with well‐balanced acceptor functionalities for absorption beyond the visible range. We have evaluated the effects of increasing acceptor strengths and incorporation of dye morphology controlling groups on molar absorptivity and absorption breadth with indolizine donor‐based dyes. Indolizine‐based D –A and D –π–A sensitizers incorporating bis‐rhodanine, tricyanofuran (TCF), and cyanoacrylic acid functionalities were analyzed for performance in DSC devices. The TCF derivatives were also evaluated as near‐infrared (NIR)‐emissive materials with the AH25 emissions extending past 1000 nm. 相似文献
Phase transfer catalvsis, PTC, has become a common preparative method in organic chemistry. Numerous aliphatic substitution reactions have been performed yielding cvanides,1 azides,2 thiocyanates,3 ethers,4 and many other types of substitution products.1相似文献
A series of nanoparticles is prepared via layer‐by‐layer assembly of oppositely charged, synthetic biocompatible polyamidoamine polymers as potential carriers. Particle size, surface charge and internal chain mobility are quantified as a function of the polymer type and number of layers. The effect of addition of surfactant is examined to simulate the effects of nanoparticle dissolution. The cyctotoxicity of these particles (in epithelia and murine cell lines) are orders of magnitude lower than polyethyleneimine controls. Stable nanoparticles may be prepared from mixtures of strongly, oppositely charged polymers, but less successfully from weakly charged polymers, and, given their acceptable toxicity characteristics, such modularly designed constructs show promise for drug and gene delivery.
The potential effect of spectral interference on the accurate measurement of the cadmium (Cd) mass fraction in fortified breakfast cereal and a variety of dietary supplement materials using inductively coupled plasma quadrupole mass spectrometry was studied. The materials were two new standard reference materials (SRMs)—SRM 3233 Fortified Breakfast Cereal and SRM 3532 Calcium Dietary Supplement—as well as several existing materials—SRM 3258 Bitter Orange Fruit, SRM 3259 Bitter Orange Extract, SRM 3260 Bitter Orange-containing Solid Oral Dosage Form, and SRM 3280 Multivitamin/Multielement Tablets. Samples were prepared for analysis using the method of isotope dilution and measured using various operating and sample introduction configurations including standard mode, collision cell with kinetic energy discrimination mode, and standard mode with sample introduction via a desolvating nebulizer system. Three isotope pairs, 112Cd/111Cd, 113Cd/111Cd, and 114Cd/111Cd, were measured. Cadmium mass fraction results for the unseparated samples of each material, measured using the three instrument configurations and isotope pairs, were compared to the results obtained after the matrix was removed via chemical separation using anion exchange chromatography. In four of the six materials studied, measurements using the standard mode with sample introduction via the desolvating nebulizer gave results for the unseparated samples quantified with the 112Cd/111Cd isotope pair that showed a positive bias relative to the matrix-separated samples, which indicated a persistent inference at m/z?112 with this configuration. Use of the standard mode, without the desolvating nebulizer, also gave results that showed a positive bias for the unseparated samples quantified with the 112Cd/111Cd isotope pair in three of the materials studied. Collision cell/kinetic energy discrimination mode, however, was very effective for reducing spectral interference for Cd in all of the materials and isotope pairs studied, except in the multivitamin/multielement matrix (SRM 3280) where the large corrections for known isobaric interferences or unidentified interferences compromised the accuracy. For SRM 3280, matrix separation provided the best method to achieve accurate measurement of Cd. 相似文献
The potential of an optical sensor based on mid-infrared spectroscopy, utilising a zinc selenide (ZnSe) attenuated total reflectance (ATR) element coated with an amorphous Teflon polymer, to determine chlorinated hydrocarbon species (CHC) in an aqueous environment is examined. The polymer coating concentrates the analytes within the penetration depth of the Fourier transform infrared (FTIR) evanescent wave and excludes water from the region. Teflon AF (Amorphous Fluoropolymer) is a family of amorphous copolymers based on polytetrafluoroethylene (PTFE), and is commercially available in two polymeric grades. Teflon AF is highly amorphous in nature with a large 'void volume', exhibits excellent chemical resistance and low water absorption. Such properties identify it as an excellent candidate for enrichment coating on an ATR/FTIR sensor. The potential of both polymeric grades of Teflon AF as enrichment membranes for ATR/FTIR analysis of CHC species was examined and contrasted. A rapid, repeatable, reversible response was observed with both grades to a range of CHC species. Linear responses in the mg/L region, with detection limits in the low mg/L region were achieved with the system used. 相似文献