Na[Li(NH2BH3)2]--the first mixed-cation amidoborane with unusual crystal structure

We describe the successful synthesis of the first mixed-cation (pseudoternary) amidoborane, Na[Li(NH(2)BH(3))(2)], with theoretical hydrogen capacity of 11.1 wt%. Na[Li(NH(2)BH(3))(2)] crystallizes triclinic (P1) with a = 5.0197(4) ?, b = 7.1203(7) ?, c = 8.9198(9) ?, α = 103.003(6)°, β = 102.200(5)°, γ = 103.575(5)°, and V = 289.98(5) ?(3) (Z = 2), as additionally confirmed by Density Functional Theory calculations. Its crystal structure is topologically different from those of its orthorhombic LiNH(2)BH(3) and NaNH(2)BH(3) constituents, with distinctly different coordination spheres of Li (3 N atoms and 1 hydride anion) and Na (6 hydride anions). Na[Li(NH(2)BH(3))(2)], which may be viewed as a product of a Lewis acid (LiNH(2)BH(3))/Lewis base (NaNH(2)BH(3)) reaction, is an important candidate for a novel lightweight hydrogen storage material. The title material decomposes at low temperature (with onset at 75 °C, 6.0% mass loss up to 110 °C, and an additional 3.0% up to 200 °C) while evolving hydrogen contaminated with ammonia.     

Structures, electronic properties and solid state luminescence of Cu(I) iodide complexes with 2,9-dimethyl-1,10-phenanthroline and aliphatic aminomethylphosphines or triphenylphosphine

The luminescent complexes of triphenylphosphine and two interesting aminomethylphosphines: P(CH(2)N(CH(2)CH(2))(2)NCH(3))(3) and P(CH(2)N(CH(2)CH(2))(2)O)(3) with copper(I) iodide and 2,9-dimethyl-1,10-phenanthroline (dmp): [CuI(dmp)PPh(3)], [CuI(dmp)P(CH(2)N(CH(2)CH(2))(2)NCH(3))(3)] and [CuI(phen)P(CH(2)N(CH(2)CH(2))(2)O)(3)] are presented in this work. These complexes were characterized in solution by means of NMR spectroscopy and their structures were crystallographically determined in the solid state. All complexes crystallize as the discrete dimers bound by π-stacking interactions between dmp rings. The coordination geometry about the Cu(I) centre is pseudo-tetrahedral showing small flattening and large rocking distortions. The investigated compounds exhibit intense orange photoluminescence in the solid state (emission peaks at r.t.: λ(max) = 588-592 nm; τ = 1.7-2.2 and 6.4-10.0 μs; at 77 K: λ(max) = 605-612 nm; τ = 4.8-6.5 and 32-47 μs), which is several orders higher than the luminescence of the analogous complexes with 1,10-phenanthroline (phen). Electronic and structural properties of the [CuI(dmp/phen)PR(3)] complexes were characterized using DFT methods to interpret their photophysics. On the basis of TDDFT calculations the broad CT bands observed in UV-Vis spectra are interpreted as the two mixed transitions from σ(CuI) bond with a small admixture of σ(CuP) bond to π* phen or dmp ligand: (MX,MPR(3))LCT, while the emissions most probably occur from two triplet states which are in thermal equilibrium.     

Stability of multi-additive mappings in non-Archimedean normed spaces

A function f:Vn→W, where V is a commutative semigroup, W is a linear space and n?1 is an integer, is called multi-additive if it is additive in each variable. In this paper we prove the generalized Hyers-Ulam stability of multi-additive mappings in non-Archimedean normed spaces, using the so-called direct method.     

Regularity of weakly subquadratic functions

Related to the theory of convex and subadditive functions, we investigate weakly subquadratic mappings, that is, solutions of the inequality

     

Applications of hybrid universality to multivariable zeta-functions

In the present paper, we obtain new results on universality as applications of hybrid universality and almost-periodicity in its half-plane of absolute convergence. By using these, we show the universality for Euler products of Igusa type, Euler-Zagier multiple zeta-functions and Tornheim-Hurwitz type of double zeta-functions.     

On Riesz Transforms Characterization of <Emphasis Type="Italic">H</Emphasis><Superscript>1</Superscript> Spaces Associated with Some Schrödinger Operators

Let \(\mathcal Lf(x)=-\Delta f (x)+V(x)f(x)\), V?≥?0, \(V\in L^1_{loc}(\mathbb R^d)\), be a non-negative self-adjoint Schrödinger operator on \(\mathbb R^d\). We say that an L ¹-function f is an element of the Hardy space \(H^1_{\mathcal L}\) if the maximal function

$ \mathcal M_{\mathcal L} f(x)=\sup\limits_{t>0}|e^{-t\mathcal L} f(x)| $

belongs to \(L^1(\mathbb R^d)\). We prove that under certain assumptions on V the space \(H^1_{\mathcal L}\) is also characterized by the Riesz transforms \(R_j=\frac{\partial}{\partial x_j}\mathcal L^{-1\slash 2}\), j?=?1,...,d, associated with \(\mathcal L\). As an example of such a potential V one can take any V?≥?0, \(V\in L^1_{loc}\), in one dimension.

     

The Eilenberg-Moore Category and a Beck-type Theorem for a Morita Context

The Eilenberg-Moore constructions and a Beck-type theorem for pairs of monads are described. More specifically, a notion of a Morita context comprising of two monads, two bialgebra functors and two connecting maps is introduced. It is shown that in many cases equivalences between categories of algebras are induced by such Morita contexts. The Eilenberg-Moore category of representations of a Morita context is constructed. This construction allows one to associate two pairs of adjoint functors with right adjoint functors having a common domain or a double adjunction to a Morita context. It is shown that, conversely, every Morita context arises from a double adjunction. The comparison functor between the domain of right adjoint functors in a double adjunction and the Eilenberg-Moore category of the associated Morita context is defined. The sufficient and necessary conditions for this comparison functor to be an equivalence (or for the moritability of a pair of functors with a common domain) are derived.     

LC�CMS�CMS Method for the Analysis of New Non-Imidazole Histamine H3 Receptor Antagonist 1-[3-(4-tert-Butylphenoxy)propyl]piperidine in Rat Serum��Application to Pharmacokinetic Studies

A sensitive and specific liquid chromatography electrospray ionisation-tandem mass spectrometry method for determination of new non-imidazole histamine H(3) receptor antagonist 1-[3-(4-tert-butylphenoxy)propyl]piperidine (DL76) in rat serum has been developed and validated. Chromatography was performed on a XBridge? C18 analytical column (2.1?×?30?mm, 3.5?μm, Waters, Ireland) with gradient elution using a mobile phase containing acetonitrile and water with an addition of 0.1% of formic acid. Detection was achieved by an Applied Biosystems MDS Sciex (Concord, Ontario, Canada) API 2000 triple quadrupole mass spectrometer. Electrospray ionization (ESI) was used for ion production. The limit of detection in the SRM mode was found to be 0.5?ng?mL(-1). The limit of quantification was 1?ng?mL(-1). The precision and accuracy for both intra- and inter-day determination of DL76 ranged from 1.65 to 15.09% and from 88.74 to 113.43%. The results of this analytical method validation allow to carry out pharmacokinetic studies in rats. The method was used for the pilot study of the pharmacokinetic behavior of DL76 in rats after intravenous administration.     

Properties of β-sitostanol/DPPC monolayers studied with Grazing Incidence X-ray Diffraction (GIXD) and Brewster Angle Microscopy

Although the influence of structurally modified sterols on artificial membranes has been intensively investigated, studies on the properties of stanols, which are saturated analogs of sterols, are very rare. Therefore, we have performed Grazing Incidence X-ray Diffraction (GIXD) experiments aimed at studying in-plane organization of a plant stanol-β-sitostanol monolayer and its mixtures with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine - DPPC at the air/water interface. The collected GIXD data, resulting in-plane parameters and BAM images provide information on molecular organization and in-plane ordering of the investigated films. It was found that the lateral organization of β-sitostanol/DPPC monolayers depends on their composition. The oblique structure of the in-plane lattice of tilted hydrophobic region of molecules, found for DPPC film, is maintained at 10 mol% of stanol in the system. However, at 30 and 90 mol% of stanol in the mixture, the arrangement of molecules is hexagonal and they are oriented perpendicularly to the interface. With the addition of stanol the extend of the in-plane order of the monolayers decreases. Moreover, in mixtures the ordered domains consist of both monolayer's components. Additionally, β-sitostanol film is of similar in-plane organization as the corresponding sterol monolayer (β-sitosterol) and stanol induces condensing effect on DPPC.