Dimethacrylate derivatives of dimer acid

Dimethacrylate monomers are used in a wide variety of crosslinked polymer applications, including adhesives, coatings, dental restoratives, and stereolithography. The advantages of rapid curing and good mechanical properties offered by these materials are countered by problems with dimensional changes during polymerization and long‐term physical instability resulting from water sorption and loss of residual unreacted monomer. In this work, several examples of hydrophobic monomers based on a dimer acid structure were synthesized, and their monomeric and homopolymer properties were evaluated. The photopolymerization reactivity and conversion were investigated with near‐infrared spectroscopy. Studies of the volumetric shrinkage, water sorption, and water contact angle and three‐point‐bend testing of the homopolymers were also carried out, with the results compared with those of commonly used dimethacrylate monomers. The new monomers produced higher degrees of conversion combined with lower polymerization shrinkage and water sorption values in comparison with conventional monomers. The relatively low crosslink density of dimethacrylates constructed from dimer acid produced polymers with high flexibility and low modulus, as expected; however, changes in the functionality of the group linking the dimer acid core with the methacrylate end groups induced significant property differences. On the basis of the properties demonstrated by the dimer acid monomers and their homopolymers, these new materials appear well suited for applications such as coatings and adhesives. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3921–3929, 2006     

Radical reactions initiated by the photochemical cleavage of carbon-indium bonds of organoindium compounds

Intra- and intermolecular reactions of carbon-centered radicals generated by photolysis of organoindium compounds were examined. The photolysis of vinylindium compounds and indium acetylides provided vinyl and alkynyl radicals, respectively, which were trapped with ethyl iodoacetate giving the corresponding β,γ-unsaturated esters. Allylic indium compounds, prepared from 8-bromo- or 8-iodooct-1,6-dienes and powdered indium metal, underwent an intramolecular radical cyclization to afford the 5-exo-trig product.     

Transfer effects on communication and collision avoidance behavior from playing a three-dimensional auditory game based on a virtual auditory display

Transfer effects on two everyday auditory skills from playing an auditory game using a virtual auditory display (VAD) were investigated using two groups of 20 normally sighted participants. Representative auditory skills of blindfolded participants were pre-tested using communication and collision avoidance tasks. They performed the tasks two weeks later. Participants in a training group played the VAD-based game on seven days (30 min/day) during the two weeks: control group participants did not. Playing the VAD-based game significantly increased face-contacts in the communication task and significantly improved participants’ collision avoidance. No significant differences were found between the groups’ subjective ratings of the rated tension levels during the communication task or between rated levels for the collision threat. Performance revealed transfer effects of playing the VAD-based game on communication behaviors in social interaction and on avoidance of approaching objects: VAD-based games are effective training tools for auditory skills used in daily life.     

Direct imaging of spatially modulated superfluid phases in atomic fermion systems

It is proposed that the spatially modulated superfluid phase, or the Fulde-Ferrell-Larkin-Ovchinnikov state could be observed in resonant fermion atomic condensates which are realized recently. We examine optimal experimental setups to achieve it by solving the Bogoliubov-de Gennes equation for both idealized one-dimensional and realistic three-dimensional cases. The spontaneous modulation of this superfluid is shown to be directly imaged as the density profiles either by optical absorption or by Stern-Gerlach experiments.     

Black string perturbations in RS1 model

Keywords We present a general formalism for black string perturbations in the Randall-Sundrum 1 model (RS1). First, we derive the master equation for the electric part of the Weyl tensor E _μν. Solving the master equation using the gradient expansion method, we give the effective Teukolsky equation on the brane at low energy. It is useful to estimate gravitational waves emitted by perturbed rotating black strings. We also argue on the effect of the Gregory-Laflamme instability on the brane using our formalism.     

Polymorphic structure and physical properties of the polyester/ether poly(ethylene-1,2-diphenoxyethane-p,p′ -dicarboxylate)

X-ray diffraction studies of fibers of the polyester/ether poly(ethylene-1,2-diphenoxyethane-p,p′ -dicarboxylate) (PEET) produced by high-speed melt spinning show the existence of two polymorphic forms, designated α and β, in the solid state. The α form is obtained by annealing filaments melt spun at takeup speeds below 3000 m/min and is also found in samples crystallized from the melt and from dilute solutions. The α form has a monoclinic unit cell with dimensions a = 7.83, b = 10.33, c = 18.68 Å, and β = 83.1°. The equilibrium melting temperature and heat of fusion of the α form are 288.3°C and 19.1 cal/g, respectively. The β form predominates in highly oriented filaments obtained at takeup velocities above 6000 m/min. The unit cell is orthorhombic with dimensions a = 7.28, b = 5.65, and c = 18.64 Å. The β form does not transform to the α form on annealing.     

A palladium catalyzed conversion of halohydrins to ketones

Pd(OAc)₂ combined with P(o-Tol)₃ catalyzes the conversion of halohydrins to ketones in the presence of K₂CO₃. Various halohydrins, which are easily available from olefins, can be converted to ketones in high yields.     

Emulsifier-free emulsion polymerization of tetrafluoroethylene by radiation. II. Effects of reaction conditions on polymer particle size and number

The size, distribution, and number of PTFE particles formed by radiation-induced emulsifier-free polymerization were measured by electron microscope and automatic particle analyzer (centrifugation method). From the electron micrographs we found that the particles are formed within 5 min. The change in the number of polymer particles (n_p) with reaction time (t) depends on the relative concentration of growing polymer chains to stabilizing species produced by the radiolysis of water and monomer; that is, it was governed by TFE pressure/dose rate ratio and classified into three cases: case I, dn_p/dt = 0 (e.g., at 3 × 10⁴ rad/hr and 20 kg/cm²); case II, dn_p/dt < 0 (e.g., at dose rate below 1.9 × 10⁴ rad/hr and 20 kg/cm²); case III, dn_p/dt > 0 (e.g., at 3 × 10⁴ rad/hr and 2 kg/cm²). The polymer molecular weight above 10⁶ is almost independent of the particle size. The polymerization loci are mainly on the surface of polymer particles dispersed in the aqueous phase in cases I and II except in the initial stage. In case III new particles are formed successively during polymerization. Therefore the polymerization loci are mainly in the aqueous phase. Especially in case I, we concluded that after the generation of particles the propagation proceeds mainly on the surface of polymer particles like the core shell model proposed by Granico and Williams.