Crystal structures and 77Se NMR spectra of molybdenum(IV) areneselenolates having intramolecular NH...Se hydrogen bonds

Salts of the monooxomolybdenum(IV,V) areneselenolates having intramolecular NH...Se hydrogen bonds, [Mo(IV)O(Se-2-RCONHC6H4)4]2- (R = t-Bu, CH3, CF3) and [Mo(V)O(Se-2-t-BuCONHC6H4)4]-, were synthesized and characterized by 1H nuclear magnetic resonance (NMR), 77Se NMR, electron spin resonance (ESR), UV-visible spectra, X-ray analysis, and electrochemical measurements. 77Se-1H correlated spectroscopy (COSY) indicated a significant correlation between amide 1H and selenolate 77Se atoms through an NH...Se hydrogen bond with 1J(77Se-1H) = 5.4 Hz coupling. The hydrogen bonds contribute to the positive shift in the Mo(V)/Mo(IV) redox potential. In the crystal structure of (PPh4)2[Mo(IV)O(Se-2-CH3CONHC6H4)4], an NH...O=Mo hydrogen bond was found. Ab inito calculations support the presence of intramolecular NH...O=Mo and NH...Se hydrogen bonds.     

Mechanism of alternating copolymerization of 4-hydroxy-4′-vinylbiphenyl with α-chloromaleic anhydride

The copolymerization of 4-hydroxy-4′-vinylbiphenyl (HVB) with α-chloromaleic anhydride (CMAn) was investigated in THF, 1,4-dioxane, and acetonitrile. The formation of the 1:1 charge transfer complex between HVB and CMAn was confirmed spectroscopically, and the corresponding equilibrium constant (K_eq) was determined as follows: K_eq = 0.19, 0.11, and 0.058 mol/L in THF, 1,4-dioxane, and CH₃CN, respectively. The copolymer composition is affected by the solvent, i.e., the content of HVB in the copolymer obtained in THF or 1,4-dioxane is lower than 50 mol % whereas the copolymer obtained in CH₃CN has excess of HVB units. The maximum rate of copolymerization was observed at a 1:1 initial comonomer mole ratio, irrespective of the solvent polarity. Plots of R_p/[HVB] vs. [HVB] gave a straight line with a slope and an intercept for the copolymerization in THF whereas a straight line in CH₃CN has no slope. On the basis of these results and ¹³C-NMR spectra of the copolymers, the mechanism of the predominant formation of alternating copolymers is discussed.     

Enzyme immunoelectrode for insulin incorporating a membrane partially treated with water vapour plasma

An enzyme immunoelectrode for the amperometric determination of serum insulin is described. The device consists of an immunoreactive membrane combined with a hydrogen peroxide electrode. The surface of a microporous hydrophobic polypropylene membrane is modified by water vapour plasma treatment to make it partially hydrophilic. Subsequent treatment with octamethylenediamine and glutaraldehyde enables the surface of this membrane to interact with various proteins. Anchoring of the antibody to Protein A immobilized on the membrane was effective for immunoreactivity.     

The scheduling of deliveries in a production-distribution system with multiple buyers

In a real production and distribution business environment with one supplier and multiple heterogeneous buyers, the differences in buyers’ ordering cycles have influence on production arrangements. Consequently, the average inventory level (AIL) at the supplier’s end is affected by both the production policy and the ordering policy, typically by the scheduling of deliveries. Consequently, the average inventory holding cost is most deeply affected. In this paper, it is proposed that the scheduling of deliveries be formulated as a decision problem to determine the time point at which deliveries are made to buyers in order to minimize the supplier’s average inventory. A formulation of the average inventory level (AIL) in a production cycle at the supplier’s end using a lot-for-lot policy is developed. Under the lot-for-lot policy, the scheduling of deliveries (SP) is formulated as a nonlinear programming model used to determine the first delivery point for each buyer with an objective to minimize the sum of the product of the individual demand quantity and the first delivery time for each buyer. Thus, the SP model determines not only the sequence of the first deliveries to individual buyers, but also the time when the deliveries are made. An iterative heuristic procedure (IHP) is developed to solve the SP model assuming a given sequence of buyers. Six sequence rules are considered and evaluated via simulation.     

Hydrobromic acid-dimethyl sulfoxide reagent for dealkylation of 5,10-dialkyl-5,10-dihydrophenazines: Synthesis of 10-alkyl-2(10H)-phenazinones

By the reaction of 5,10-dialkyl-substituted 5,10-dihydrophenazine with hydrobromic acid in dimethyl sulfoxide at 90–110°, 10-alkyl-2(10H)-phenazinone was obtained as a major product. Brominated dihydrophenazine was isolated in the case of 1,6-dichloro-5,10-dimethyl-5,10-dihydrophenazine.     

Development of ultra-short pulse VUV laser system for nanoscale processing

We have developed intense vacuum ultraviolet (VUV) radiation sources for advanced material processing, such as photochemical surface reactions and precise processing on a nanometer scale. We have constructed a new VUV laser system to generate sub-picosecond pulses at the wavelength of 126 nm. A seed VUV pulse was generated in Xe as the 7th harmonic of a 882-nm Ti:sapphire laser. The optimum conversion was achieved at the pressure of 1.2 Torr. The seed pulse will be amplified by the Ar₂^*\mathrm{Ar}_{2}^{*} media generated by an optical-field-induced ionization Ar plasma produced by the Ti:sapphire laser. We have obtained a gain coefficient of g=0.16 cm⁻¹. Our developing system will provide VUV ultra-short pulses with sub-μJ energy at a repetition rate of 1 kHz.     

Observation of vacuum-ultraviolet Ar2* radiation gain at 126 nm produced by an ultrashort high-intensity laser pulse propagating in a hollow fiber

We observed a small-signal gain of Ar2* emission at 126 nm by use of a hollow fiber to guide the high-intensity laser propagation in high-pressure Ar. The small-signal gain coefficient was measured to be 0.05 cm(-1) at 126 nm. Kinetic analysis revealed that the electrons produced by the high-intensity laser through an optical-field-induced ionization process initiated the Ar2* production processes. The increase in the emission intensity was measured to be exp(2.5), with an increase in the fiber length.     

Low-temperature performance of thin solid electrolyte cell based on MoO3-doped Bi2O3

Improvement of low-temperature performance of oxygen sensor was studied by preparing a thin film of 15 μm thickness. Melt-quenched Bi₂O₃ film doped with 16 mol% MoO₃ was used as an electrolyte after HF treatment. Impedance measurements were carried out in the frequency range DC-100 KHz. Resistance of electrolyte in the form of thin film (110ω) was negligibly small compared with the overall resistance of the cell (287 Kω) at 350°C. Oxygen/air concentration cell was constructed and the cell performance was measured at 350 and 300°C. Transference number close to unity and rapid response were observed at 350°C, however the cell showed a long response time of about 3 min at 300°C.     

Covariant quantization of string based on BRS invariance

Covariant canonical quantization of the bosonic string is performed, based on the BRS invariance principle. Defining a physical state by a modified form of Kugo-Ojima's subsidiary condition Q_B|phys〉 = 0 (Q_B = BRS charge), we prove a no-ghost theorem in a simple manner. There an interesting relation between critical dimension and BRS symmetry is noticed; namely, the conditions D = 26 and α₀ = 1 for the space-time dimension D and the zero-intercept α₀ of leading trajectory are required by the nilpotency Q_B² = 0 of the BRS charge. In addition, ghost number fractionization is observed in this system.     

SPECTRAL ANALYSIS OF CHLOROPHYLL a AGGREGATES IN THE PRESENCE OF WATER-SOLUBLE MACROMOLECULES

Abstract— The absorption and fluorescence spectra of chlorophyll a (Chi a) aggregates formed in aqueous solutions of polyvinyl alcohol) (PVA), polyvinyl pyrrolidone) (PVP), and bovine serum albumin (BSA) were analyzed by curve-fitting methods in the wavelength region from 650 to 800 nm. The results indicated that the aggregation of Chi a to polymeric forms such as (Chia–2H₂0), was suppressed in the presence of the macromolecules. The suppression was due to a coordination of macromolecule bound ligands to Chi a and was strongest in BSA and weaker in PVA. There were differences in the spectra even though the same types of polymeric Chi a forms were observed due to characteristically different composition of these forms. Fluorescence patterns indicated that energy was transferred from the shorter to the longer wavelength forms.