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1.
Well-organized thiol monolayers on electrode surfaces are prepared using the Langmuir–Blodgett and self-assembly methods. Planned modification of the molecules building the monolayer allow the electron tunneling efficiency across the monolayer to be controlled. The barrier properties of the monolayers are probed by electrochemical methods. The extent of blocking for all systems under study indicates that contribution of the electroactive molecules that find direct access to the electrode surface can be neglected. These observations permit us to use the monolayers for the determination of the kinetic parameters of Fe(CN)3–
6 and IrCl2–
6 ion reduction. Such monolayers are employed for the studies of long-range electron transport. We show that insertion of amide bonds in appropriate positions of the alkyl chains of all molecules building the monolayer makes it possible to create a lateral hydrogen-bond network linking the internal amide groups in the monolayer and contributing to the electronic coupling between the redox probe and the electrode. The relation between the location of the amide moiety in the molecule and its importance for the electron tunneling efficiency through the intervening organic medium is discussed. 相似文献
2.
Anna Maria Zawisza 《Tetrahedron letters》2007,48(38):6738-6742
The Pd-catalyzed homocoupling of aryl halides in a basic DMF solution is often accompanied by the dehalogenation of the substrate as side reaction. When an inorganic base such as sodium bicarbonate is used, the reducing role of the solvent has been demonstrated using DMF-d7 and GC/MS analysis. 相似文献
3.
An efficient and stereoselective synthesis of pyrrolidine-, piperidine-, and azepane-type N-heterocycles is described by the intramolecular Pd(0)-catalysed cyclisation of amino allylic carbonates. The use of chiral ligands gave the corresponding heterocyclic derivatives having er values that were from moderate to good. 相似文献
4.
M. Zawisza 《Physics of Particles and Nuclei Letters》2011,8(9):924-927
Correlations between non-identical particles at small relative velocity probe asymmetries in the average space-time emission
points at freeze-out. The origin of such asymmetries may be from long-lived resonances, bulk collective effects, or differences
in the freeze-out scenario for the different particle species. STAR has extracted pion-proton correlation functions from a
dataset of Au+Au collisions at √s
NN
= 200 GeV. We present correlation functions in the spherical harmonic decomposition representation, for different centralities
and for different combinations of pions and (anti-)protons. 相似文献
5.
Rafal Sitko Beata Zawisza Ewa Talik Paulina Janik Grzegorz Osoba Barbara Feist Ewa Malicka 《Analytica chimica acta》2014
Graphene oxide (GO) is a novel material with excellent adsorptive properties. However, the very small particles of GO can cause serious problems is solid-phase extraction (SPE) such as the high pressure in SPE system and the adsorbent loss through pores of frit. These problems can be overcome by covalently binding GO nanosheets to a support. In this paper, GO was covalently bonded to spherical silica by coupling the amino groups of spherical aminosilica and the carboxyl groups of GO (GO@SiO2). The successful immobilization of GO nanosheets on the aminosilica was confirmed by scanning electron microscopy and X-ray photoelectron spectroscopy. The spherical particle covered by GO with crumpled silk wave-like carbon sheets are an ideal sorbent for SPE of metal ions. The wrinkled structure of the coating results in large surface area and a high extractive capacity. The adsorption bath experiment shows that Cu(II) and Pb(II) can be quantitatively adsorbed at pH 5.5 with maximum adsorption capacity of 6.0 and 13.6 mg g−1, respectively. Such features of GO nanosheets as softness and flexibility allow achieving excellent contact with analyzed solution in flow-rate conditions. In consequence, the metal ions can be quantitatively preconcentrated from high volume of aqueous samples with excellent flow-rate. SPE column is very stable and several adsorption–elution cycles can be performed without any loss of adsorptive properties. The GO@SiO2 was used for analysis of various water samples by flame atomic absorption spectrometry with excellent enrichment factors (200–250) and detection limits (0.084 and 0.27 ng mL−1 for Cu(II) and Pb(II), respectively). 相似文献
6.
Malicka E Sitko R Zawisza B Heimann J Kajewski D Kita A 《Analytical and bioanalytical chemistry》2011,399(9):3285-3292
The paper presents possibilities and difficulties in nondestructive analysis of small multielement single crystals performed
by means of X-ray spectrometry techniques: micro-X-ray fluorescence spectrometry (μ-XRF), energy-dispersive electron probe
microanalysis (ED-EPMA), and X-ray photoelectron spectroscopy (XPS). The capability of the X-ray spectroscopy techniques in
elemental analysis is demonstrated with the single crystals of selenide spinels of the general formula M
x
N
y
Cr
z
Se4 (M+2 and N+3 are, for example, Zn+2, V+3, Ga+3, Cd+2, In+3, and Sb+3). The results of the nondestructive analyses (μ-XRF, ED-EPMA, and XPS) are compared with those obtained by inductively coupled
plasma optical emission spectrometry (ICP-OES) and wavelength-dispersive X-ray spectrometry (WDXRF) following sample digestion.
The present study shows satisfactory agreement between the results of μ-XRF analysis performed using the standardless fundamental
parameter method and the results obtained with the WDXRF and ICP-OES analyses. If the measured single crystal is precisely
positioned, the difference between μ-XRF and wet analysis (WDXRF and ICP-OES) does not exceed 5% rel. The reliable results
of ED-EPMA can be obtained only if the measured area is sufficiently large, i.e., of 200 × 300 μm. Even if this condition
is fulfilled, the relative difference between the ED-EPMA and the wet analysis may reach 10% rel. In case of the XPS analysis,
the accuracy of results depends on the proper preparation of the sample surface. It should be free of contamination that can
be obtained by scraping in situ in ultrahigh vacuum. The ion etching, commonly used for cleaning the surface, leads to preferential
sputtering; therefore, the reliable results cannot be obtained. 相似文献
7.
8.
Zawisza I Nullmeier M Pust SE Boukherroub R Szunerits S Wittstock G 《Langmuir : the ACS journal of surfaces and colloids》2008,24(14):7378-7387
Ultrathin titanium layers when deposited on the surface of gold can be successfully applied for infrared reflection absorption spectroscopy (IRRAS) investigations. It was shown that the reflectivity, the phase shift, and the mean square electric field of the p- and s-polarized IR radiation in up to 20 nm thick titanium layers covered with a 3-4 nm thick layer of native oxide are comparable to those of the air/gold interface. The surface selection rule is fulfilled. Thus, qualitative and quantitative analysis of 1,2-dimyristoyl- sn-glycero-3-phosphocholine (DMPC) bilayers transferred in liquid expanded (LE) and liquid condensed (LC) states can be performed. Differences are found in the hydration state and molecular arrangement of the two investigated bilayers. In the DMPC bilayer in the LE state, the C-N bond in the positively charged choline moiety is inclined by approximately 70 degrees toward the surface of the negatively charged titanium substrate. In the phosphate moiety, the in-plane vector of the O-P-O group makes a small angle of approximately 15 degrees to the surface normal. This open structure of the lipid molecule corresponds to the B crystal structure of the DMPC molecule and provides space for strong hydration of the polar headgroup. In the DMPC bilayer in the LC state, the intermolecular distances are reduced; the C-N bond of the choline group makes a smaller angle to the surface normal, and the in-plane vector of the O-P-O group in the phosphate moiety displays a larger tilt. The degree of hydration is reduced. The arrangement of the polar headgroup region corresponds to the A crystal structure of the DMPC molecule. 相似文献
9.
PM IRRAS investigation of thin silica films deposited on gold. Part 1. Theory and proof of concept 总被引:1,自引:0,他引:1
Zawisza I Wittstock G Boukherroub R Szunerits S 《Langmuir : the ACS journal of surfaces and colloids》2007,23(18):9303-9309
Polarization modulation infrared reflection absorption spectroscopy (PM IRRAS) was successfully used for the first time to characterize an optically transparent thin oxide film. SiO2 layers of 7 nm thickness were synthesized by plasma enhanced chemical vapor deposition (PECVD) on 200 nm thick gold covered glass slides. Despite the fact that silica is transparent and absorptive to IR radiation when deposited in the form of thin films on a gold surface, it preserves the high metallic reflectivity for the IR light. At grazing angles of incidence of the IR beam, the enhancement of the normal component of the electric field at the interface is comparable to that of Au alone. In addition, the analysis of the structure of a 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) lipid monolayer deposited using the Langmuir-Blodgett technique is demonstrated. 相似文献
10.
Bilayers of 1-octadecanol were transferred from the gas-solution interface onto a Au(111) electrode surface using either the horizontal touch or the Langmuir-Blodgett (LB) technique. The horizontal touch method gives an X-type film in which the molecule in the bottom layer is oriented with the tail toward the metal and the head toward the tail of the molecule in the top layer (head to tail orientation). The LB technique allows one to build not only X but also a Y bilayer, in which the molecules in the two leaflets are oriented tail to tail with the polar heads facing the metal and the solution. The properties of these films were characterized by electrochemistry and polarization modulation infrared reflection absorption spectroscopy (PM IRRAS). The freshly prepared X bilayer is defect free and is characterized by a low capacity of 0.84 microF cm(-2). The bilayer may be desorbed from the electrode surface at E < -0.6 V and readsorbed again at more positive potentials. The potential-driven readsorption gives a Y film with a higher capacity of 2.2 microF cm(-2). The IR studies of a mixed bilayer composed of one hydrogenated leaflet and a second deuterated leaflet showed that 1-octadecanol molecules assume a more vertical orientation in the leaflet facing the solution than in the leaflet in contact with the metal. Upon desorption of the X film, the molecules in the bottom layer flip-flop and the readsorbed film assumes the Y structure. Smaller tilt angles are observed in the X film as opposed to the Y film. 相似文献