The umbral calculus and orthogonal polynomials

We determine all orthogonal polynomials having Boas-Buck generating functions g(t)(xf(t)), where% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacqqHOo% qwcaGGOaGaamiDaiaacMcacqGH9aqpruqqYLwySbacfaGaa8hiamaa% BeaaleaacaaIWaaabeaakiaadAeacaqGGaWaaSbaaSqaaiaabgdaae% qaaOGaaeikaiaadggacaGGSaGaa8hiaiaadshacaqGPaGaaeilaiaa% bccacaqGGaGaaeiiaiaadggacqGHGjsUcaaIWaGaaiilaiaa-bcacq% GHsislcaaIXaGaaiilaiaa-bcacqGHsislcaaIYaGaaiilaiablAci% ljaacUdaaeaacqqHOoqwcaGGOaGaamiDaiaacMcacqGH9aqpcaWFGa% WaaSraaSqaaiaaicdaaeqaaOGaamOraiaabccadaWgaaWcbaGaaeOm% aaqabaGccaGGOaWaaSqaaSqaaiaaigdaaeaacaaIZaaaaOGaaiilai% aa-bcadaWcbaWcbaGaaGOmaaqaaiaaiodaaaGccaGGSaGaa8hiaiaa% dshacaGGPaGaa8hiamaaBeaaleaacaaIWaaabeaakiaadAeacaqGGa% WaaSbaaSqaaiaabkdaaeqaaOGaaeikamaaleaaleaacaaIYaaabaGa% aG4maaaakiaacYcacaWFGaWaaSqaaSqaaiaaisdaaeaacaaIZaaaaO% Gaaiilaiaa-bcacaWG0bGaaiykaiaacYcacaWFGaWaaSraaSqaaiaa% icdaaeqaaOGaamOraiaabccadaWgaaWcbaGaaeOmaaqabaGccaGGOa% WaaSqaaSqaaiaaisdaaeaacaaIZaaaaOGaaiilaiaa-bcadaWcbaWc% baGaaGynaaqaaiaaiodaaaGccaGGSaGaa8hiaiaadshacaGGPaGaai% 4oaaqaaiabfI6azjaacIcacaWG0bGaaiykaiabg2da9iaa-bcadaWg% baWcbaGaaGimaaqabaGccaWGgbGaaeiiamaaBaaaleaacaqGZaaabe% aakiaacIcadaWcbaWcbaGaaGymaaqaaiaaisdaaaGccaGGSaGaa8hi% amaaleaaleaacaaIYaaabaGaaGinaaaakiaacYcacaWFGaWaaSqaaS% qaaiaaiodaaeaacaaI0aaaaOGaaiilaiaa-bcacaWG0bGaaiykaiaa% -bcadaWgbaWcbaGaaGimaaqabaGccaWGgbGaaeiiamaaBaaaleaaca% qGZaaabeaakiaabIcadaWcbaWcbaGaaGOmaaqaaiaaisdaaaGccaGG% SaGaa8hiamaaleaaleaacaaIZaaabaGaaGinaaaakiaacYcacaWFGa% WaaSqaaSqaaiaaiwdaaeaacaaI0aaaaOGaaiilaiaa-bcacaWG0bGa% aiykaiaacYcaaeaadaWgbaWcbaGaaGimaaqabaGccaWGgbGaaeiiam% aaBaaaleaacaqGZaaabeaakiaacIcadaWcbaWcbaGaaG4maaqaaiaa% isdaaaGccaGGSaGaa8hiamaaleaaleaacaaI1aaabaGaaGinaaaaki% aacYcacaWFGaWaaSqaaSqaaiaaiAdaaeaacaaI0aaaaOGaaiilaiaa% -bcacaWG0bGaaiykaiaacYcacaGGUaGaa8hiamaaBeaaleaacaaIWa% aabeaakiaadAeacaqGGaWaaSbaaSqaaiaabodaaeqaaOGaaeikamaa% leaaleaacaaI1aaabaGaaGinaaaakiaacYcacaWFGaWaaSqaaSqaai% aaiAdaaeaacaaI0aaaaOGaaiilaiaa-bcadaWcbaWcbaGaaG4naaqa% aiaaisdaaaGccaGGSaGaa8hiaiaadshacaGGPaGaaiOlaaaaaa!C1F3!\[\begin{gathered}\Psi (t) = {}_0F{\text{ }}_{\text{1}} {\text{(}}a, t{\text{), }}a \ne 0, - 1, - 2, \ldots ; \hfill \\\Psi (t) = {}_0F{\text{ }}_{\text{2}} (\tfrac{1}{3}, \tfrac{2}{3}, t) {}_0F{\text{ }}_{\text{2}} {\text{(}}\tfrac{2}{3}, \tfrac{4}{3}, t), {}_0F{\text{ }}_{\text{2}} (\tfrac{4}{3}, \tfrac{5}{3}, t); \hfill \\\Psi (t) = {}_0F{\text{ }}_{\text{3}} (\tfrac{1}{4}, \tfrac{2}{4}, \tfrac{3}{4}, t) {}_0F{\text{ }}_{\text{3}} {\text{(}}\tfrac{2}{4}, \tfrac{3}{4}, \tfrac{5}{4}, t), \hfill \\{}_0F{\text{ }}_{\text{3}} (\tfrac{3}{4}, \tfrac{5}{4}, \tfrac{6}{4}, t),. {}_0F{\text{ }}_{\text{3}} {\text{(}}\tfrac{5}{4}, \tfrac{6}{4}, \tfrac{7}{4}, t). \hfill \\\end{gathered}\]We also determine all Sheffer polynomials which are orthogonal on the unit circle. The formula for the product of polynomials of the Boas-Buck type is obtained.     

Γ andX bandgap hydrostatic deformation potentials for epitaxial In0.52Al0.48As on InP(001)

The pressure dependence of the direct and indirect bandgap of epitaxial In_0.52Al_0.48As on InP(001) substrate has been measured using photoluminescence up to 92 kbar hydrostatic pressure. The bandgap changes from Γ toX at an applied pressure of ∼ 43 kbar. Hydrostatic deformation potentials for both the Γ andX bandgaps are deduced, after correcting for the elastic constant (bulk modulus) mismatch between the epilayer and the substrate. For the epilayer we obtain and+(2.81±0.15)eV for the Γ andX bandgaps respectively. From the pressure dependence of the normalized Γ-bandgap photoluminescence intensity a Γ-X lifetime ratio, (τ_Γ/τ _X ), of 4.1×10⁻³ is deduced.     

Polyethene with pendant fullerene moieties

Polyethene with fullerene moieties pendant on short-chain branches was prepared by the catalytic copolymerization of ethene and a fullerene-containing vinylic comonomer, yielding polyethene copolymers containing up to 25 wt% of C60.     

Thermal Stability Of Folic Acid in the solid-state

This study attempts to identify the degradative process which folic acid undergoes in the solid-state under thermal stress. In order to facilitate the process, the various pieces of the chemical structure, namely, p-amino benzoic acid, pterin and glutamic acid as both its d- and l-isomers were investigated as separate entities. These structured solid-state pieces were then compared to the composite solid state folic acid degradative curves in order to identify the peaks seen and provide direction for the interpolation of the degradative mechanism. It was observed that none of the structural pieces could be superimposed as assumed earlier and hence an attempt was made to identify the decomposition products using various analytical techniques such as infrared spectroscopy, mass spectroscopy and X-ray diffraction which suggested that the glutamic acid fragment is lost first as evidenced by acid loss and amide enhancement in the IR spectra. The vitamin was ultimately degrading to carbon fragments and that further identification was not necessary. This revised version was published online in August 2006 with corrections to the Cover Date.     

Characterization of some essential oils and their key components: Thermoanalytical techniques

The present study was aimed at determining the kinetics of evaporation and establishing vapor pressure curves for both single and multi-component systems by thermogravimetry (TG) and differential scanning calorimetry (DSC). Essential oils (e.g. lavender oil, orange oil, clove oil and eucalyptus oil, etc.) are typically multi-component systems consisting of various volatile pure components (e.g. linalyl acetate, limonene, cinnamaldehyde, etc.) which resemble single component systems. In this study linalyl acetate was taken as the calibration compound for TG. The vapor pressure curves for the pure substances were plotted using TG and vapor pressure plots for clove oil and eucalyptus oil were constructed using DSC. The thermodynamic and kinetic parameters of the pure compounds were compared to that of the multi-component systems to quantitatively and qualitatively measure the influence of different compounds on each other. The k-value from the vapor pressure data for linalyl acetate was calculated as 112006 Pa kg^0.5mol^0.5s^-1 m^-2 K^-0.5. The vapor pressure values were used to determine the Antoine constants using the SPSS 10.0 software.This revised version was published online in November 2005 with corrections to the Cover Date.     

Platinum metallodrug-protein binding studies by capillary electrophoresis-inductively coupled plasma-mass spectrometry: characterization of interactions between Pt(II) complexes and human serum albumin

Characterizing how platinum metallocomplexes bind to human serum albumin (HSA) is essential in evaluating anticancer drug candidates. Using cisplatin as a reference complex, the application of capillary electrophoresis (CE) to reliably assess drug/HSA interactions was validated. Since this complex is small compared to the size of the protein, the binding response could only be recognized when applying CE coupled to a (platinum) metal-specific mode of detection, namely inductively coupled plasma-mass spectrometry (ICP-MS). This coupling allowed for confirmation of a specific affinity of cisplatin and novel Pt complexes to HSA, measurement of the kinetics of binding reactions, and determination of the number of drug molecules attached to the protein. As the cisplatin/HSA molar ratio increased, the reaction rate became faster with a maximum on the kinetic curve appearing at about 50 h of incubation at 20 times excess of cisplatin. The reaction was characterized as a pseudo-first order reaction with the rate constant k = 0.003 min(-1) at 37 degrees C. When incubated with a 20-fold excess of cisplatin, HSA bound up to 10 mol of Pt per mol of the protein. This is indicative for a strong metal-protein coordination occurring at several HSA sites other than the only protein cysteine residue. Structural analogs of cisplatin, bearing aminoalcohol ligands, showed comparable protein binding reactivity and stoichiometry but a common equilibrium was not reached even after one week of incubation. Also apparent was a two-step mechanism of the binding reaction. Results demonstrated the suitability of CE-ICP-MS as a rapid assay for high-throughput studying of drug/HSA interactions.     

Accreditation of reference material producers: the example of IRMM's Reference Materials Unit

The potential approaches for third-party assessment of reference material producers are revisited and the activities of the Reference Materials (RM) Unit of the Institute for Reference Materials and Measurements (IRMM) to obtain accreditation to ISO Guide 34 and ISO 17025 are described. Accreditation was related to the Unit as all matrix RM activities of the institute are concentrated there. A management system was established that allows sufficient flexibility to be applicable to a wide range of RMs while being precise enough to ensure compliance with ISO Guides 30, 31 and especially 34 and 35. Accreditation was achieved in 2004 with independent scopes for testing and RM production and was confirmed and extended in 2005. The key aspects of the RM Unit's management system for RM production are presented. Presented at BERM-10, April 2006, Charleston, SC, USA