An Improved Procedure for Cyclisation of Chalcones to Flavanones Using Celite Supported Potassium Fluoride in Methanol: Total Synthesis of Bavachinin

Chalcones may be cyclised to the corresponding flavanones by stirring with KF-celite suspended in methanol at reflux. This method gives consistently higher conversion than other reported procedures and its utility is illustrated by the synthesis of the linear prenylated flavanone bavachinin.     

Phase-field modeling of void evolution and swelling in materials under irradiation

Void swelling is an important phenomenon observed in both nuclear fuels and cladding materials in operating nuclear reactors. In this work we develop a phase-field model to simulate void evolution and void volume change in irradiated materials. Important material processes, including the generation of defects such as vacancies and self-interstitials, their diffusion and annihilation, and void nucleation and evolution, have been taken into account in this model. The thermodynamic and kinetic properties, such...     

“Living” free radical graft copolymers I: Preparation and properties

Polymers substituted with thio groups are useful for the photochemical synthesis of graft copolymers. Such copolymers have been prepared by the initial conversion of backbone polymers containing chlorinated substituents into polymers containing diethyldithiocarbamate (TC), isopropyl xanthate (IX) or mercaptobenzothiazole (BT) functionality. The photochemical reaction of monomers with these products produced graft copolymers. A variety of halogenated polymers were investigated as starting materials for these syntheses, including poly(vinyl chloride), chlorinated polyvinyl chloride), chlorinated polyethylene, chlorobutyl rubber and neoprene. Characteristics of the grafting reactions, including “pseudo-living” behavior and tandem grafting aspects, were investigated. Glass transitions of the grafted polymers were found to vary uniformly with composition for most of the grafted products.     

Thermodynamic properties of phenol–formaldehyde resin

Characterization measurements of a commercial phenol-formaldehyde resin prepared from constituents including phenol and formaldehyde in the molar ratio 1:1.33 are reported. The measurements consist of (1) the linear thermal expansion coefficient between approximately 85 and 270°K; (2) the specific heat capacity between approximately 6 and 100°K; (3) the Young's modulus at room temperature. A critical examination of the data reveals that: (1) the vibrational behavior is predominantly that of a three-dimensional assembly; (2) as far as data available from other sources permit an assessment to be made, the principle of additivity appears to be applicable to the specific heat capacity between approximately 50 and 100°K; and (3) the data lie near the limit of an empirical relationship observed between the Young's modulus and linear thermal expansion coefficient of other polymers.     

A search for the exotic Ξ<Superscript>−−</Superscript> (1860) in the hyperon beam experiment WA89(1860) in the hyperon beam experiment WA89

We report on a high statistics search for the Ξ^??(1860) resonance in Σ^?-nucleus collisions at 340 GeV/c. No evidence for this resonance is found in our data sample which contains 676000 Ξ^? candidates above bakground. For the decay channel Ξ^??(1860)→Ξ^? π ^? and the kinematic range 0.15<xF<0.9 we find a 3σ upper limit for the production cross section of 3.1 and 3.5 μb per nucleon, for reactions with carbon and copper, respectively.     

The proton and carbon chemical shift assignments of 2-substituted thioxanthones

The complete proton and carbon chemical shift assignments have been made for thioxanthone, 2-fluorothioxanthone, 2-chlorothioxanthone, 2-bromothioxanthone, 2-N, N-dimethylsulfonamidothioxanthone, 2-methylthioxanthone, 2-methoxythioxanthone and 2-acetylthioxanthone. Assignments were made with the aid of both COSY and CSCM two-dimensional nmr techniques. The C2 substituent alters chemical shifts in the unsubstituted heterocyclic ring.