Pauli Equation for Non-Abelian Dyons in Moduli Space

Undertaking the study of behaviour of an extended dyon moving in the generalized electromagnetic field of another non-Abelian dyon in moduli space, Dirac's equation has been solved for energy eigenvalues and it has been shown that spin momentum of an interacting non-Abelian dyon behaves as extra energy source. Introducing suitable spinors, the Pauli equation for a spin-1/2 non-Abelian dyon moving in the field of another non-Abelian dyon has been solved in moduli space and it has been shown that ad hoc introduction of spin in the system of two non-Abelian dyons perceptibly modifies the energy eigenvalues and eigenfunctions of bound states of the system.     

Prompt Gamma Neutron Activation Analysis of 316-L Stainless Steel

Prompt gamma-rays from thermal neutron capture reaction have been used to measure the concentrations of the main constituents namely Fe, Ni and Cr in 316-L stainless steel using recently established prompt gamma neutron activation analysis (PGNAA) facility at Pakistan Institute of Nuclear Science and Technology (PINSTECH). High resolution, high purity germanium detector with 40% relative efficiency was employed for the gamma-ray spectroscopy of the samples. The interference-free full energy gamma-ray peaks of the elements of interests were selected in the high energy low background region (5.0–9.0 MeV). The efficiency calibration of the detector was performed using ultra pure standards of chromium and chlorine obtained respectively from Merck and Alpha Inorganics. This paper describes, in addition, the salient features as well as the background of establishing PGNAA facility at the Institute.     

Zeros of the densities of infinitely divisible measures on R n

Let be an infinitely divisible probability measure onR ⁿ without Gaussian component and let be its Lévy measure. Suppose that is absolutely continuous with respect to the Lebesgue measure . We investigate the structure of the set ⁿ of admissible translates of . This yields a unified presentation of previously known results. We also show that if(S)>0 then is equivalent to , under the assumption that supp =R ⁿ , whereS is the closure of the semigroup generated by the support of .The research of this author is supported by KBN Grant.The research of this author is supported by AFSOR Grant No. 90-0168, and the University of Tennessee Science Alliance, a State of Tennessee Center of Excellence.     

Semistable laws on topological vector spaces

Summary In this paper we discuss three types of results: Firstly, we present two Lévy-Hinin type representations of Poisson type infinitely divisible (i.d.) laws on certain topological vector (TV) spaces; one of these complements a known representation due to Dettweiler. Secondly, we define and characterize r-semistable laws on locally convex TV spaces and also obtain good representation of their characteristic functions. Finally, we discuss the existence and the continuity of the semigroup { _tt>0} of i.d. laws on locally convex TV spaces. These complement similar known results of Siebert.The research of this author is partially supported by the Office of Naval Research under contract No. N0014-78-C-0468     

Synthesis, characterization and cytotoxicity of some palladium(II), platinum(II), rhodium(I) and iridium(I) complexes of ferrocenylpyridine and related ligands. Crystal and molecular structure of trans-dichlorobis(3-ferrocenylpyridine)palladium(II)

The preparation of a series of ferrocenyl nitrogen donor ligands including ferrocenylpyridines, ferrocenylphenylpyridines and 1,1^′-di(2-pyridyl)ferrocene is described. Coordination studies of the substituted pyridines (L) were carried out with platinum, palladium, rhodium and iridium. This resulted in the preparation of the following types of complexes: [MCl(CO)₂(L)] and [M(cod)(L)₂]ClO₄ where M=Rh or Ir, cod=1,5-cyclooctadiene; [M^′Cl₂(L)₂] where M^′=Pt or Pd. The X-ray crystal structure of trans-dichlorobis(3-ferrocenylpyridine)palladium was obtained. The complexes were screened for activity against two human cancer cell lines. At least two of the complexes displayed growth inhibition similar to that of the widely used chemotherapeutic agent, cisplatin.     

Synthesis,characterization, DNA binding and cleavage activity of homoleptic zinc(II) β-oxodithioester chelate complexes

New homoleptic zinc(II) complexes, [Zn(L)₂], where L = methyl-3-hydroxy-(3-pyridyl)-2-propenedithioate L1 1, and methyl-3-hydroxy-(4-pyridyl)-2-propenedithioate L2 2, have been synthesized and characterized by elemental (C, H, and N) analysis, ESI-MS, and (IR, UV–vis, NMR) spectroscopy; the structure of 1 has been deduced by X-ray crystallography. The DNA binding and cleavage activity of the complexes have been studied. The cleavage potential of pBR322 DNA by 1 and 2 has been checked. Complex 1, which contains nitrogen of the pyridine group in the 3-position enhances DNA cleavage potential in the presence of ascorbic acid; however, the complex is protective against DNA cleavage in the presence of DMSO or H₂O₂. Also, 1 causes cytotoxicity against the MCF-7 breast cancer cell line. The efficient cytotoxic activity and DNA cleavage ability of 1 in the presence of ascorbic acid shows its potential anticancer properties and the need for further investigations of its potential as an anticancer drug.     

Modification of sulfonated poly(ether ether ketone) with phenolic resin

Soluble phenol formaldehyde resin containing hydroxymethyl groups has been used to modify sulfonated poly(ether ether ketone) (SPEEK). Modification has been carried out with films containing both the polymers and using dimethyl formamide (DMF) as casting solvent at various temperatures under reduced pressure. Associated solvent and the hydrogen‐bonded by‐product dimethyl amine (DMA) were removed through mild alkali–acid–water treatment. Cured and treated films show good and consistent mechanical properties, water uptake (22–25%), ion‐exchange capacity (1.1–1.5 meq/g) and proton conductivity (125–150 mS/cm) at 30°C and hold promise for application in fuel cells, as indicated by a polarization study in a fuel cell test station. Copyright © 2007 John Wiley & Sons, Ltd.     

An efficient synthesis of rearranged new biologically active benzimidazoles derived from 2-formyl carvacrol

Research on Chemical Intermediates - A new series of benzimidazole derivatives was synthesized by one-pot two-step reaction as a result of unexpected rearrangement during reaction of 2-formyl...     

Strategy to design aqueous-soluble iron-oxide molecular cluster and nanostructure using polyoxometalate ligand scaffold

Profound availability of iron on earth crust and diversely accessible redox states, makes it a significant metal ion in biology as well as to design molecular catalysts and nanostructured materials. Low-oxidation potential and prone to hydrolysis in an aqueous medium, predominantly in neutral to basic pH, of the divalent iron in the active site of the catalysts, results in the formation of bulk and/or colloidal ferric-hydroxide, oxy-hydroxide, and -oxide. However, nature has developed its own strategy to preserve iron-oxide cluster core, e.g., Ferritin, without aggregation in physiological pH via designing protein scaffold as protector ligand. Although molecular iron-oxo clusters, isolated by using small organic ligands, are depicted as potent catalysts, they usually don't sustain under catalytic turnover condition. In this context, the isolation of multinuclear iron-oxo clusters soluble in water and their subsequent catalysis in the aqueous phase remains a perdurable challenge. Polyoxometalates (POM) are themselves small metal-oxo cluster anions where the metals are in the highest valent-state and a diverse POM structure can be obtained simply by varying the metal ions. Depending on the structure of the POM, the available terminal or bridging oxo groups can act as donor atoms to one or more iron centers. Consequently, a variety of iron clusters can be stabilized by using POM scaffold. Thereby, polyoxoanions, extremely aqueous-soluble and oxidatively inert under reaction conditions, behaved as versatile ligand platform to stabilize iron clusters of different nuclearity (n = 2–30) in water. Moreover, different possible structures and diversity in chemical property by varying hetero atoms or metal ions led to the isolation of a unique aqueous soluble iron-oxide and/or iron-oxy-hydroxide nanostructure where a significant number of polyoxoanions were covalently attached, making them extremely soluble nanostructures. This review summarizes the adapted synthetic strategies to isolate such molecular and nano-scopic iron clusters stabilized by POM anions and describes their stability in an aqueous medium and showcases their prospective applications in different emerging areas.     

one-pot synthesis of pyrrolo-[3,4-d]isoxazoline-4,6-diones via nitrile oxides

1,3-Dipolar cycloaddition of nitrile oxides generated in situ in the presence of variously substituted N-arylmaleimides and N-benzylmaleimide provides new pyrrolo[3,4-d]izoxazoline-4,6-diones in good yields. The whole procedure could be performed in a practical and efficient one-pot operation. All the cycloadducts were isolated in excellent yields and identified by spectral studies. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 444–448, March, 2009.