National Repository of Grey Literature 60 records found  beginprevious38 - 47nextend  jump to record: Search took 0.01 seconds. 
Structural, Redox and Spectrometric Characterization of Energetic Material FOX-7 (2,2-dinitroethene-1,1-diamine) in Solution
Šimková, Ludmila ; Ludvík, Jiří
The investigation of energetic materials, especially organic nitro-amino-derivatives, always has attracted attention of physical chemists. However, published articles demonstrate lack of systematic study of molecules based on aliphatic backbones, rather than aromatic structures. This work represents the first systematic electrochemical and spectrometric characterization of 2,2-dinitroethene-1,1-diamine (FOX-7) in aqueous and aprotic solvent. Based on the results obtained from combination of electrochemistry with spectrometric methods, the actual structure of FOX-7 in various media was revealed, its reducibility described and radical intermediates as well as products were intercepted, isolated and characterized.
Role of Intramolecular Electron Interactions in Cathodic Reduction of Three Isomeric Benzenedialdehydes in Non-aqueous Media – a (Spectro)Electrochemical Study
Kantnerová, Kristýna ; Klíma, Jiří ; Ludvík, Jiří
This contribution is focused on cathodic reduction of three isomeric benzenedialdehydes – orthophthalaldehyde (OPA), isophthalaldehyde (IPA) and terephthalaldehyde (TPA) – in non-aqueous acetonitrile and dimethylformamide. Although their electrochemical behavior in aqueous solutions has been published several times, their investigation in organic aprotic solvents is lacking. Using DC-polarography, cyclic voltammetry, preparative electrolyses, coulometry and UV/Vis spectroelectro-chemistry their reduction was described and in the case of OPA and TPA, stable radical anions were characterized by EPR spectroscopy. The role of intramolecular electron interactions in their cathodic reduction is discussed.
Electrochemical Reduction of FOX-7 in Aprotic Solvent Accompanied by Formation of a Radical with Alternating Line-width Effect
Šimková, Ludmila ; Lušpai, K. ; Klíma, Jiří ; Ludvík, Jiří
Different structures of FOX-7 in various solutions play a crucial role in the mechanism of its electrochemical reduction. In aprotic solvent the irreversible four-electron, four-proton reduction of one nitro group proceeds according to the autoprotonation mechanism. The zwitterionic form of FOX-7 serves as a source of protons. The two-step reduction is accompanied by an adsorption step in dependence on used solvent and material of electrode. The in situ spectroelectrochemical measurements revealed formation of a dianion radical intermediate with alternating line-width effect. The intramolecular dynamic processes were described by temperature dependent in situ ESR measurement.
Electrochemical Study of Oxazaborine Chromophores
Mikysek, T. ; Josefík, F. ; Vytřas, K. ; Ludvík, Jiří
This contribution describes a basic electrochemical study of a series of newly synthesized chromophores based on the oxazaborine core. The attention was focused on determination of the first oxidation and the first reduction potentials, their difference and the relationship to the calculated highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies. The oxidation is mostly a two-electron irreversible process, the first reduction is also irrevesible, but involving one-electron. For better understanding of the relationship between the structure and redox properties, the approach using sigma (para) constants of Hammett type was applied, the difference between E(ox) and E(red) was correlated with the HOMO-LUMO gap.
The Use of Self-Assembled Monolayer of Thiolated Calix[4]arene on Polycrystaline Gold Electrode Surface
Hrdlička, V. ; Navrátil, Tomáš ; Šestáková, Ivana ; Barek, J. ; Ludvík, Jiří
This study deals with the use of thiolated calixarene (C[4]A) as gold electrode modifier, alone or in combination with insulating undecanthiol (C11SH), which is used to fill the gaps between calixes. Desorption potential of thiolated C[4]A and C11SH are both pH dependent, cathodic desorption peaks can be recorded in basic solutions only. The properties of the modified electrode were investigated using hydroquinone - electrochemically active molecule which fits inside the C[4]A cavity. Obtained data suggest that the electrochemical oxidation/reduction ofhydroquinone does not use C[4]A cavities as size-selective channels.
Electrochemistry of Polynitrocalix-[4]-arenes
Liška, Alan ; Ludvík, Jiří
Calix[4]arene is a suitable inert and stable frame for building "smart" molecules and supramolecular assemblies. Polynitrocalix[4]arenes where reducible nitro groups are located at the upper rim are promising precursors for aimed development of sensors. In this work a series of mono-, di-, tri- and tetra nitroderivatives was reduced, the sequence of individual steps was described and the mechanism discussed. It was found that in this molecule with several redox centers all nitro groups are electronically isolated and thus are reduced independently yielding poly-radical ions. Two different couples of equivalent nitro groups were proved in tetranitro derivatives. The experimental results were confirmed by quantum chemical calculations.
New Characterisation Approaches for Carbon Ionic Liquid Electrodes (CILES)
Mikysek, T. ; Stočes, M. ; Švancara, I. ; Vytřas, K. ; Ludvík, Jiří
Within this study, some new approaches to characterize the carbon paste mixtures and the respective carbon ionic liquid electrodes (CILEs) are presented and their properties discussed. Particular attention has been paid to the changes of the resistivity, relative to the dependence on composition of the CILE. Three types of carbon ionic liquid pastes were examined, and for the interpretation of experimental data, the results were compared with those of "classic" carbon paste electrode (CPE) based on graphite powder. Some problems connected with homogeneity and stability of carbon pastes are also discussed.
Electrochemical Reduction of 1,3-Alt-tetranitrothiacalix[4]arenes
Liška, Alan ; Ludvík, Jiří
Calixarenes are organic molecules which contain several aromatic units (in this work four) connected by methylene („calixarenes“) or sulfur („thiacalixarenes“) bridges. Calix[4]arenes can exist in four defined conformations: cone-, partial cone-, 1,2- and 1,3-alternating (Fig. 1). The conformational stability of a (thia)calix[4]arene is controlled by the size of the substituents on the upper or the lower rim, or by other interactions (e.g. hydrogen bonds). These compounds are very attractive for supramolecular chemists, since they have the shape of a cavity, being able to exhibit host-guest interaction according to the substitution 1,2. The calixarene skeleton itself is not reducible. Therefore it´s necessary to introduce a suitable redox probe in the calixarene frame in order to use electrochemical methods for investigations of calixarene properties. For the purpose of this study the nitro group was chosen because its electrochemical reduction proceeds easily in a well-defined way.
Electrochemical Study of Triazaborine Chromophores
Mikysek, T. ; Josefík, F. ; Ludvík, Jiří
This contribution describes a basic electrochemical behaviour of a series of newly synthesized chromophores based on triazaborine core. The main attention has been paid to the investigation of the first oxidation and first reduction process of such compounds using cyclic voltammetry, rotating disk voltammetry and polarography. The oxidation is mostly a two-electron irreversible process, whereas the first reduction is in most cases revesible, involving one-electron. For better understanding of the relationship between the structure and redox properties, the Linear Free Energy relationship (LFER) approach using sigma (para) constants of Hammett type was applied, the oxidation and reduction centers were localized, the difference between E(ox) and E(red) was correlated with the HOMO-LUMO gap and the anomalous cases were elucidated.
Funding of public universities with focus on qualitative criteria
Ludvík, Jiří ; Urbánek, Václav (advisor) ; Kubík, Rudolf (referee)
The bachelor's thesis as a whole deals with funding of public universities in the Czech Republic. The bachelor's thesis deals at first with education system in the Czech Republic and defines the term "university education" as such itself. Step by step gets it to the problematics of funding public universities and describes this process in the Czech Republic in detail. As a main issue the bachelor's work analyses qualitative touchstones in funding of public universities and finally investigates the impact of these intermediate indicators on budget of the University of Economics in Prague.

National Repository of Grey Literature : 60 records found   beginprevious38 - 47nextend  jump to record:
Interested in being notified about new results for this query?
Subscribe to the RSS feed.