Novel amphiphilic network polymers consisting of nonpolar,short primary polymer chains and polar,long crosslink units: Influence of characteristic dangling chains on swelling behavior of resulting amphiphilic gels

Novel amphiphilic network polymers consisting of nonpolar, short primary polymer chains and polar, long crosslink units were prepared, and the swelling behavior of resulting amphiphilic gels is discussed by focusing on the influence of characteristic dangling chains; that is, benzyl methacrylate (BzMA) was copolymerized with tricosaethylene glycol dimethacrylate [CH₂?C(CH₃)CO(OCH₂CH₂)₂₃OCOC(CH₃)?CH₂, PEGDMA‐23] in the presence of lauryl mercaptan as a chain‐transfer agent because BzMA forms nonpolar, short primary polymer chains and PEGDMA‐23 as a crosslinker contains a polar, long poly(oxyethylene) unit. The enhanced incorporation of dangling chains into the network polymer was brought by shortening the primary polymer chain length, and copolymerization with methoxytricosaethylene glycol methacrylate, a mono‐ene counterpart of PEGDMA‐23, enforced the incorporation of flexible dangling poly(oxyethylene) chains into the network polymer, although the former dangling chains as terminal parts of primary poly(BzMA) chains were rather rigid. Then, the influence of characteristic dangling chains on the swelling behavior of amphiphilic gels was examined in mixed solvents consisting of nonpolar t‐butylbenzene and polar methanol. The profiles of the solvent‐component dependencies of the swelling ratios were characteristic of amphiphilic gels. The introduction of dangling poly(oxyethylene) chains led not only to an increased swelling ratio but also to sharpened swelling behavior of amphiphilic gels. The swelling response of amphiphilic gels was checked by changing the external solvent polarity. The dangling chains with freely mobile end segments influenced the swelling response of gels. The amphiphilic gels with less entangled, collapsed crosslink units exhibited faster swelling response than the ones with more entangled, collapsed primary polymer chains. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2192–2201, 2004     

Light attenuation in a semitransparent foam sheet-Thickness measurement for industrial use

An optical method for measuring the thickness of heterogeneous materials has been studied. The method is based on the light attenuation theory. A complete system has been constructed in order to demonstrate the applicability of the present method for industrial use. The experimental set-up consists of semiconductor lasers, focusing lenses, photo-diodes serving as a power meter and a personal computer with an A/D converter for data acquisition. Averaging of numerous measurements is required in the present method because the heterogeneous cell structure of the foam material yields large fluctuations in transmitted light levels. The fluctuations can be reduced to below 1% of the transmitted light power by 80 times averaging. The error of the measurement is considered to be a few tens of micrometers in thickness. The present system is capable of sampling data at a rate of 400 Hz and has been successfully applied to a manufacturing process.     

Die Copolymerisation von Vinylhydrochinon und Acrylnitril mit Tri-n-Butylboran

Ohne Zusammenfassung     

Surface photochemistry: The photo-chlorination of aromatic hydrocarbons with ferric chloride on alumina

Irradiation of a number of aromatic hydrocarbons adsorbed on alumina in the presence of ferric chloride leads to monochlorination.     

Hochtemperaturphosphidierung von Eisen-Nickellegierungen mittels Phosphordampf

High Temperature Phosphidation of Iron-Nickel Alloys by Phosphorus Vapor A study was undertaken concerning the products and kinetics in the phosphidation of iron-nickel alloys with various ratios of metallic constituents at 700° in phosphorus vapor at 1 atm by a sealed-tube method. X-ray diffraction patterns and an electron microprobe analysis of the products showed that the phosphide-layer structure reaches the expression of NiP₂ ～ Ni₆P₅/Ni₂P, Fe₂P/(Fe? Ni alloy). The phosphidations proceeded according to a parabolic rate law for all the compositions of the alloy. A marker experiment indicated that the diffusing species was not phosphorus but metals. The rate constant decreased with an increase in the content of iron in the alloy.     

Complete asymmetric induction in heteroconjugate addition on an acyclic system a new synthetic approach directed toward ansamacrolide maytansine

Acyclic asymmetric induction was achieved in >99 % $\text{threo}$ formation via coordinated intermediate ($\text{3}$) in the heteroconjugate addition ($\text{2}$ to $\text{4}$); the heteroatom in the adduct being used for elongation of the carbon chain toward maytansine $\text{1}$).     

Carbon-13 NMR studies of the biologically active nor-diterpenoid dilactones from Podocarpus plants

Carbon-13 NMR signals of the biologically active norditerpenoid dilactones from Podocarpus plants were fully assigned by using selective ¹H decoupling, coupling constants (²J_CH), spin-lattice relaxation times (T₁) and correlation of the spectra of more than thirty dilactone congeners. The spectra of five nagilactones, B, C, D, E and F, which constitute representative members of three major structural types of the dilactones: (A) 8:14, 9:11-dienolide (α-pyrone) type, (B) 7α:8α-epoxy-9:11-enolide type, and (C) 7:8,9:11-dienolide type, were extensively analysed. Some characteristic steric interactions for the substituents on the ring system can be demonstrated from the spectral properties.