Long-range electronic interactions at a high temperature: bromine adatom islands on Cu(111)

Long-range electronic interactions between Br adatom islands, which are formed at approximately 600 K, on Cu(111) are mediated by substrate surface-state electrons at that elevated temperature. Using scanning tunneling microscopy at 4 K, we have quantified nearest neighbor island separations and found favored spacings to be half-multiples of the Fermi wavelength of Cu(111). The strong interaction potential and decay length of the interisland interactions are discussed in terms of the interaction of Br with the substrate surface state.     

Asymptotic Energy Expansion for Rational Power Polynomial Potentials

Asymptotic energy expansion method is extended for polynomial potentials having rational powers. New types of recurrence relations are derived for the potentials of the form V(x)=x^2n/m+b₁x^n1/m1+b₂x^n2/m2 +··· + b_Nx^n_N/m_N where n,m,n₁,m₁,...,n_N,m_N are positive integers while coefficients b_k∈ C. As in the case of even degree polynomial potentials with integer powers, all the integrals in the expansion can be evaluated analytically in terms of Γ functions. With the help of two examples, we demonstrate the usefulness of these expansions in getting analytic insight into the quantum systems having rational power polynomial potentials.     

Bremsstrahlung shielding parameters in polymer concretes

Concretes are used for shielding in nuclear power plants. Beta radiation is emitted during the nuclear reactions. This beta radiation interacts with the concrete and results in secondary radiation such as bremsstrahlung. Shielding parameters of beta-induced bremsstrahlung in concretes are important in the field of radiation protection. We have evaluated the cross section, yield, intensity and dose rate of beta-induced bremsstrahlung by pure beta nuclides of end point energy ranges from 0.4 to 5?MeV in some polymer-based concretes such as sulfur polymer concrete, barium polymer concrete, calcium polymer concrete, fluorine polymer concrete, chlorine polymer concrete and germanium polymer concrete. We have compared the shielding properties among the studied polymer concretes. The efficiency, intensity and dose rate of bremsstrahlung increases with a maximum energy of beta nuclide and modified atomic number of the concrete. From the detailed study, it is clear that the barium polymer concrete is having large bremsstrahlung dose rate and specific bremsstrahlung constant values than the other studied polymer concretes. This means barium polymer concrete is a good absorber of bremsstrahlung radiation than the other studied polymer concretes.     

Asymptotic Energy Expansion for Rational Power Polynomial Potentials

Asymptotic energy expansion method is extended for polynomial potentials having rational powers. New types of recurrence relations are derived for the potentials of the form V(x)= x2n/m+b1xn1/m1+b2x n2/m2+ …+ bNxnN/mN where n, m, n1, m1, . . . , nN, mN are positive integers while coefficients bk∈C. As in the case of even degree polynomial potentials with integer powers, all the integrals in the expansion can be evaluated analytically in terms of Γ functions. With the help of two examples, we demonstrate the usefulness of these expansions in getting analytic insight into the quantum systems having rational power polynomial potentials.     

Structures of kokzeylanol and kokzeylanonol two new natural tri- and tetra- oxygenated D:A-friedo-oleananes

Kokzeylanol and kokzeylanonol obtained from $\text{Kokoona}$$\text{zeylanica}$ have been shown to be 6β,27-dihydroxy-D:A-friedo-olean-3-one ($\text{1}$) and 6β,27-dihydroxy-D:A-friedo-oleana-3,21-dione ($\text{2}$), respectively by the deoxygenatlon of their 27-acetoxy derivatives using Lithium-ethylene diamine reduction coupled with spectroscopic and irradiation methods. Kokzeylanonol represents the first tetraoxygenated D:A-friedo-oleanane isolated from a natural source.     

Higher-order semiclassical energy expansions for potentials with non-integer powers

In this paper, we present a semiclassical eigenenergy expansion for the potential |x|^α when α is a positive rational number of the form2n/m (n is a positive integer and m is an odd positive integer). Remarkably, this expansion is found to be identical to the WKB expansion obtained for the potentialx ^N(N-even), if2n/m is replaced byN. Taking the limitm → 2 of the above expansion, we obtain an explicit asymptotic energy expansion of symmetric odd power potentials |x|^2j+1 (j- positive integer). We then show how to develop approximate semiclassical expansions for potentials |x|^α when α is any positive real number.     

LC Method for the Determination of NPC1161, Primaquine and their Metabolites in Various Biological Systems

NPC1161 is an 8-aminoquinoline anti-malarial analog, which has a favorable toxicity profile relative to primaquine and other 8-aminoquinolines. High-performance liquid chromatographic method was developed for the determination of NPC1161, primaquine and their metabolites in biological samples in order to facilitate metabolic and pharmacokinetic studies. The method includes extraction of the unchanged drugs and their metabolites from the biological samples. Separation was achieved by reversed-phase chromatography on a C18 column with water–acetonitrile both containing 0.025% trifluoroacetic acid as the mobile phase. Recoveries of NPC1161 and its metabolites were greater than 60% in various biological samples tested. No interference with the components of the biological material was observed. The detector response was linear with concentrations of NPC1161 and its metabolites (desalkyl NPC1161 and carboxy NPC1161) in the ranges from 0.5 to 80.0, 0.4–60.0 and 0.4–70.0 μg mL⁻¹, respectively. A mass spectrometry coupled with electrospray ionization (ESI) interface method is described for the identification of NPC1161 and its metabolites in biological samples. This method involved the use of the [M + H]⁺ions of NPC1161, C3 analog (internal std. for the assay), desalkyl NPC1161 and carboxy NPC1161 at m/z 434, 406, 349 and 449 in the positive ion mode with extractive ion monitoring (EIM). This method will have an important application in pharmacokinetic studies of NPC1161 and in understanding the mechanism of metabolism of this novel 8-aminoquinoline analog in more detail.     

GC-MS Analysis of the 8-Aminoquinoline Antimalarial [NPC1161] and its Carboxy Metabolite in Plasma and Red Blood Cells of Primates

This study describes a novel and simple GC-MS procedure developed for the determination of the concentration of the 8-aminoquinoline antimalarial agent NPC1161 and its carboxy metabolite in plasma and red blood cells. Preliminary pharmacokinetic data were generated for the two enantiomers of NPC1161 in monkeys. NPC1161, the internal standard, and desalkyl metabolite were converted to their mono-heptafluorobutyrates, while the carboxy metabolite underwent an intramolecular cyclization to give a lactam product. The calibration curves were linear ranging from 10 to 2,000 ng mL⁻¹. The developed GC-MS method is sensitive and reproducible for measuring blood level of this antimalarial drug.     

Determination of bromide and nitrite by indirect redox titration using phenyl iodosoacetate

Bromide has been determined by its oxidation with an excess of phenyl iodosoacetate in the presence of acetanilide to give bromine which subsequently reacts with acetanilide to form 4-bromoacetanilide. The residual amount of phenyl iodosoacetate was evaluated iodometrically. Thus, for every mol of bromide one mol of phenyl iodosoacetate was consumed. For the determination of bromine in organic compounds, the test substance was decomposed by fusion with alkali peroxide to liberate bromide which was then evaluated by the phenyl iodosoacetate method. For its determination, nitrite has been reacted with an excess of isoniazid in acid medium to form isonicotinyl azide (which does not react with phenyl iodosoacetate) and the residual amount of isoniazid was titrated with phenyl iodosoacetate in the presence of acidified bromide and methyl red indicator (when isoniazid and phenyl iodosoacetate react in a 12 molar ratio). Each mol of nitrite is equivalent to 2 mol of phenyl iodosoacetate.     

Reversible Mechanical Interlocking of D‐Shaped Molecular Karabiners bearing Coordination‐Bond Loaded Gates: Route to Self‐Assembled [2]Catenanes

Complexation of 1,4‐phenylenebis(methylene) diisonicotinate, L1 , with cis‐protected Pd^II components, [Pd( L′ )(NO₃)₂], in an equimolar ratio yielded binuclear complexes, 1 a – d of [Pd₂( L′ )₂( L1 )₂](NO₃)₄ formulation where L′ stands for ethylenediamine (en), tetramethylethylenediamine (tmeda), 2,2′‐bipyridine (bpy), and phenanthroline (phen). The combination of 4,4′‐bipyridine, L2 , with the cis‐protected Pd^II units is known to yield molecular squares, 2 a – d . However, 2 b – d coexist with the corresponding molecular triangles, 3 b – d . Combination of an equivalent each of the ligands L1 and L2 with two equivalents of cis‐protected Pd^II components in DMSO resulted in the D ‐shaped heteroligated complexes [Pd₂( L′ )₂( L1 )( L2 )](NO₃)₄, 4 a – d . Two units of the D ‐shaped complexes interlock, in a concentration dependent fashion, to form the corresponding [2]catenanes [Pd₂( L′ )₂( L1 )( L2 )]₂(NO₃)₈, 5 a – d under aqueous conditions. Crystal structures of the macrocycle [Pd₂(tmeda)₂( L1 )( L2 )](PF₆)₄, 4 b′′ , and the catenane [Pd₂(bpy)₂( L1 )( L2 )]₂(NO₃)₈, 5 c , provide unequivocal support for the proposed molecular architectures.