Stereoselective synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes via intramolecular radical cyclizations mediated by CAN

The stereoselective intramolecular cyclizations of bis(cinnamyl)tosylamides and dimethyl bis(cinnamyl)malonates mediated by cerium(IV) ammonium nitrate leading to the synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes are described.     

Synthesis of aromatic aldehydes via NiCl2 reduction and hydrolysis of oxazolines

Reduction of 2-aryl-oxazolines with NiCl₂/NaBH₄ followed by hydrolysis gives the corresponding aldehydes in good yields.     

Free boundary viscous flows at micro and mesolevel during liquid composites moulding process

Numerical simulation aspects, related to low Reynolds number free boundary viscous flows at micro and mesolevel during the resin impregnation stage of the liquid composite moulding process (LCM), are presented in this article. A free boundary program (FBP), developed by the authors, is used to track the movement of the resin front accurately by accounting for the surface tension effects at the boundary. Issues related to the global and local mass conservation (GMC and LMC) are identified and discussed. Unsuitable conditions for LMC and consequently GMC are uncovered at low capillary numbers, and hence a strategy for the numerical simulation of such flows is suggested. FBP encompasses a set of subroutines that are linked to modules in ANSYS. FBP can capture the void formation dynamics based on the analysis developed. We present resin impregnation dynamics in two dimensions. Extension to three dimensions is a subject for further research. Several examples are shown and efficiency of different stabilization techniques are compared. Copyright © 2004 John Wiley & Sons, Ltd.     

Determination of nickel in alloys and plant leaves with salicylaldehyde 3-oxobutanoylhydrazone by spectrophotometry.

A simple and highly sensitive reagent of salicylaldehyde 3-oxobutanoylhydrazone (salicylaldehyde acetoacetic acid hydrazone, SAAH) was synthesized and studied for the spectrophotometric determination of nickel in detail. In the pH range 6, which greatly increased the selectivity, nickel reacted with SAAH to form a 1:1 yellow complex, having a sensitive absorption peak at 405 nm. Under the optimal conditions, Beer's law was obeyed over the range from 0.0117 to 0.1174 microg cm(-3). The apparent molar absorptivity was 3.025 x 10(5) dm3 mol(-1) cm(-1). The detection limit and the variation coefficient were found to be 1.752 ng cm(-3) and 1.0%, respectively. The method has been applied to the quantitative determination of nickel in different alloys and leaves.     

Efficient synthesis of 1,4-dihydronaphthalenelignans from 5-methylene-4-substituted-2(5H)-furanones and a concise synthesis of solafuranone

A short synthetic strategy for synthesis of lignan analogues involving 5-methylene-4-substituted-2(5H)-furanones as the key intermediates has been developed. Various lignans including the natural product solafuranone and analogues of dihydrotaiwanin C and deoxydehydropodophyllotoxin were synthesized in good yields.     

Working group report: Neutrino and astroparticle physics

This is the report of neutrino and astroparticle physics working group at WHEPP-7. Discussions and work on CP violation in long baseline neutrino experiments, ultra high energy neutrinos, supernova neutrinos and water Cerenkov detectors are discussed.     

Analysis of a Duopoly Supply Chain and its Application in Electricity Spot Markets

This paper studies a supply chain consisting of two suppliers and one retailer in a spot market, where the retailer uses the newsvendor solution as its purchase policy, and suppliers compete for the retailer’s purchase. Since each supplier’s bidding strategy affects the other’s profit, a game theory approach is used to identify optimal bidding strategies. We prove the existence and uniqueness of a Nash solution. It is also shown that the competition between the supplier leads to a lower market clearing price, and as a result, the retailer benefits from it. Finally, we demonstrate the applicability of the obtained results by deriving optimal bidding strategies for power generator plants in the deregulated California energy market. Supported in part by RGC (Hong Kong) Competitive Earmarked Research Grants (CUHK4167/04E and CUHK4239/03E), a Distinguished Young Investigator Grant from the National Natural Sciences Foundation of China, and a grant from Hundred Talents Program of the Chinese Academy of Sciences.     

Kinetic evidence of a common mechanism in the oxidations of diethyl sulfide by dichromates and halochromates of heterocyclic bases

The oxidations of diethyl sulfide by potassium dichromate, pyridinium dichromate, quinolinium dichromate, imidazolium dichromate, nicotinium dichromate, isonicotinium dichromate, pyridinium fluorochromate, quinolinium fluorochromate, imidazolium fluorochromate, pyridinium chlorochromate, quinolinium chlorochromate, and pyridinium bromochromate follow identical kinetic orders—first‐order each with respect to the chromium(VI) reagents, sulfide and hydrogen ion, and moderately inhibited by manganese(II) ion. The energy of activation varies linearly with the logarithm of frequency factor and so does the enthalpy of activation with the entropy of activation. Also, the activation free energies do not differ significantly. The dichromates and halochromates of heterocyclic bases oxidize diethyl sulfide via a common mechanism. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 35: 1–8, 2003     

Block copolymer mediated synthesis of amphiphilic gold nanoparticles in water and an aqueous tetrahydrofuran medium: An approach for the preparation of polymer–gold nanocomposites

The synthesis of polymer‐matrix‐compatible amphiphilic gold (Au) nanoparticles with well‐defined triblock polymer poly[2‐(N,N‐dimethylamino)ethyl methacrylate]‐b‐poly(methyl methacrylate)‐b‐poly[2‐(N,N‐dimethylamino)ethyl methacrylate] and diblock polymers poly(methyl methacrylate)‐b‐poly[2‐(N,N‐dimethylamino)ethyl methacrylate], polystyrene‐b‐poly[2‐(N,N‐dimethylamino)ethyl methacrylate], and poly(t‐butyl methacrylate)‐b‐poly[2‐(N,N‐dimethylamino)ethyl methacrylate] in water and in aqueous tetrahydrofuran (tetrahydrofuran/H₂O = 20:1 v/v) at room temperature is reported. All these amphiphilic block copolymers were synthesized with atom transfer radical polymerization. The variations of the position of the plasmon resonance band and the core diameter of such block copolymer functionalized Au particles with the variation of the surface functionality, solvent, and molecular weight of the hydrophobic and hydrophilic parts of the block copolymers were systematically studied. Different types of polymer–Au nanocomposite films [poly(methyl methacrylate)–Au, poly(t‐butyl methacrylate)–Au, polystyrene–Au, poly(vinyl alcohol)–Au, and poly(vinyl pyrrolidone)–Au] were prepared through the blending of appropriate functionalized Au nanoparticles with the respective polymer matrices {e.g., blending poly[2‐(N,N‐dimethylamino)ethyl methacrylate]‐b‐poly(methyl methacrylate)‐b‐poly[2‐(N,N‐dimethylamino)ethyl methacrylate‐stabilized Au with the poly(methyl methacrylate)matrix only}. The compatibility of specific block copolymer modified Au nanoparticles with a specific homopolymer matrix was determined by a combination of ultraviolet–visible spectroscopy, transmission electron microscopy, and differential scanning calorimetry analyses. The facile formation of polymer–Au nanocomposites with a specific block copolymer stabilized Au particle was attributed to the good compatibility of block copolymer coated Au particles with a specific polymer matrix. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1841–1854, 2006