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41.
Dalibor Stankovic Dragan Manojlovic Goran Roglic Sladjana Kostic‐Rajacic Ivan Andjelkovic Biljana Dojcinovic Jelena Mutic 《Electroanalysis》2011,23(8):1928-1933
The determination of Pb and Cd with a Nafion‐modified glassy carbon electrode and Cu‐DPABA complex (Cu‐DPABA–NA/GCE; DPABA is methyl 3,5‐bis{bis‐[(pyridin‐2‐yl)methyl]amino}methyl‐benzoate) as an alternative electrode for anodic stripping voltammetry was described. Pb and Cd were accumulated in acetate buffer pH 4 at a potential of ?1.4 V (vs. Ag/AgCl electrode) for 120 s followed by a DPASV scan from ?1.2 to ?0.2 V. Under optimum conditions the calibration curves were linear in the range of 4.8×10?9–5.0×10?5 and 5.0×10?9–5×10?5 mol L?1 for Pb and Cd, respectively. Detection limits were 1.8×10?9 and 1.2×10?9 mol L?1 for Pb and Cd, respectively. Different parameters and conditions, such as membrane ingredients, accumulation time, potential and pH value were optimized. A study of interfering substances was also performed. A significant increase in current was achieved at the modified electrode in comparison with the bare glassy carbon electrode. The validation of the proposed method was made by Pb and Cd determination in the certified reference material Groundwater CRM 610 (BCR, Community Bureau of Reference, Brussels, Belgium). The electrode was successfully applied for determination of Pb and Cd in river water with a high content of organic contaminants without any pretreatment. 相似文献
42.
Wu D Wang Q Assary RS Broadbelt LJ Krilov G 《Journal of chemical information and modeling》2011,51(7):1634-1647
We present a new computational strategy for the design and evaluation of novel enzymatic pathways for the biosynthesis of fuels and chemicals. The approach combines the use of the Biochemical Network Integrated Computational Explorer (BNICE) framework and a structure-based screening method for rapid generation and evaluation of novel enzymatic reactions and pathways. The strategy is applied to a case study of 1-butanol production from pyruvate, which yielded nine novel biosynthetic pathways. Using screening criteria based on pathway length, thermodynamic feasibility, and metabolic flux analysis, all nine novel pathways were deemed to be attractive candidates. To further assess their feasibility of implementation, we introduced a new screening criterion based on structural complementarity using molecular docking methods. We show that this approach correctly reproduces the native binding poses for a wide range of enzymes in key classes related to 1-butanol production and provides qualitative agreement with experimental measures of catalytic activity for different substrates. In addition, we show that the structure-based methods can be used to select specific proteins that may be promising candidates to catalyze novel reactions. 相似文献
43.
Yasuda T Shimizu T Liu F Ungar G Kato T 《Journal of the American Chemical Society》2011,133(34):13437-13444
A series of propeller-shaped π-conjugated molecules based on 2,4,6-tris(thiophene-2-yl)-1,3,5-triazines has been designed and synthesized to obtain ambipolar charge-transporting liquid-crystalline materials. The 3-fold electron-donating aromatic units are attached to the electron-accepting triazine core, which forms electro-functional octupolar π-conjugated structures. These octupolar molecules self-organize into one-dimensional columnar nanostructures and exhibit ambipolar carrier transport behavior, which has been revealed by time-of-flight measurements. In this approach, electron-donor and acceptor electro-active segments are assembled individually in each column to give one-dimensional nanostructured materials with precisely tuned electronic properties. Their desirable electronic structures responsible for both hole and electron conductions have also been examined by cyclic voltammetry and theoretical calculations. The present results provide a new guideline and versatile approach to the design of ambipolar conductive nanostructured liquid-crystalline materials. 相似文献
44.
Henig J Mamedov I Fouskova P Tóth É Logothetis NK Angelovski G Mayer HA 《Inorganic chemistry》2011,50(14):6472-6481
A novel class of 1,4,7,10-tetraazacyclododecane-1,4,7-tris(methylenecarboxylic) acid (DO3A)-based lanthanide complexes with relaxometric response to Ca(2+) was synthesized, and their physicochemical properties were investigated. Four macrocyclic ligands containing an alkyl-aminobis(methylenephosphonate) side chain for Ca(2+)-chelation have been studied (alkyl is propyl, butyl, pentyl, and hexyl for L(1), L(2), L(3), and L(4), respectively). Upon addition of Ca(2+), the r(1) relaxivity of their Gd(3+) complexes decreased up to 61% of the initial value for the best compounds GdL(3) and GdL(4). The relaxivity of the complexes was concentration dependent (it decreases with increasing concentration). Diffusion NMR studies on the Y(3+) analogues evidenced the formation of agglomerates at higher concentrations; the aggregation becomes even more important in the presence of Ca(2+). (31)P NMR experiments on EuL(1) and EuL(4) indicated the coordination of a phosphonate to the Ln(3+) for the ligand with a propyl chain, while phosphonate coordination was not observed for the analogue bearing a hexyl linker. Potentiometric titrations yielded protonation constants of the Gd(3+) complexes. log K(H1) values for all complexes lie between 6.12 and 7.11 whereas log K(H2) values are between 4.61 and 5.87. Luminescence emission spectra recorded on the Eu(3+) complexes confirmed the coordination of a phosphonate group to the Ln(3+) center in EuL(1). Luminescence lifetime measurements showed that Ca-induced agglomeration reduces the hydration number which is the main cause for the change in r(1). Variable temperature (17)O NMR experiments evidenced high water exchange rates on GdL(1), GdL(2), and GdL(3) comparable to that of the aqua ion. 相似文献
45.
Goran Djanković 《Archiv der Mathematik》2011,97(6):535-547
In this paper we investigate the sixth moment of the family of L-functions associated to holomorphic modular forms on GL 2 with respect to a congruence subgroup Γ1(q). The bound for central values averaged over the family, consistent with the Lindelöf hypothesis, is obtained for prime levels q. 相似文献
46.
Goran Radojev Torsten Linß 《Numerical Methods for Partial Differential Equations》2019,35(6):2305-2317
Collocation with triquadratic C1‐splines for a singularly perturbed reaction–diffusion problem in three dimension is studied. A posteriori error bound in the maximum norm is derived for the collocation method on arbitrary tensor‐product meshes which is robust in the perturbation parameter. Numerical results are presented that support our theoretical estimate. 相似文献
47.
The Ramanujan Journal - In this paper we investigate the distribution of degrees of the least common multiples of random subsets of monic polynomials of degree n in $${\mathbb {F}}_q[t]$$ . We... 相似文献
48.
In this paper we determine the composition series of the generalized principal seriesδ⋊σ assuming thatσ is strongly positive discrete series. 相似文献
49.
R.Michael Barnett Goran Senjanović L. Wolfenstein D. Wyler 《Physics letters. [Part B]》1984,136(3):191-195
Phenomenological consequences of a light neutral Higgs scalar S (mass < 3.7 GeV) are explored in various two-Higgs-doublet models where some of the couplings are strongly enhanced. In one class of models the two-gluon decay mode is predominant, and decays into two muons are quite suppressed. A detailed analysis of the decay b → s + S is given. The consequences a light scalar for supersymmetric models are discussed. 相似文献