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Reactivity of transition metals - influence of the degree of oxidation of active substrate
Kettner, Miroslav ; Nehasil, Václav (advisor)
The impacts of fluorine doping of ceria are studied by means of surface science experimental methods. Fluorine-doped and fluorine-free ceria layers are epitaxially grown on rhodium single crystals and their properties are compared in regular and inverse catalyst configurations. A procedure for epitaxial growth of CeO2(110) and CeOxFy(110) layers on Rh(110) single crystal is developed and described in detail. Shape alterations of Ce 3d spectrum brought about by fluorine doping are explained and a suitable deconvolution method is proposed. Special attention is focused towards stability of fluorine in ceria. Presented data show that fluorine incorporation in ceria lattice causes stable reduction of ceria, which withstands up to 200řC in near-ambient pressure conditions. Morphological changes are observed due to elongation of surface lattice constant of reduced ceria. Oxygen storage capacities and hydrogen oxidation reaction rates of four different studied systems are compared and discussed. The twofold nature of oxygen exposure of fluorinated ceria is discovered and explained. Oxygen repels fluorine from the surface, while the remaining part of fluorine is expelled to adsorbate positions, where its electronic state is altered. Moreover, such fluorine is prone to interact with atomic hydrogen. This reaction is...
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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Light platinum group metal complexes with a ferrocene N-phosphinoamide
Navrátil, Michal ; Štěpnička, Petr (advisor) ; Gyepes, Róbert (referee)
Title: Light platinum group metal complexes with a ferrocene N-phosphinoamide Author: Bc. Michal Navrátil Department: Department of Inorganic chemistry Supervisor: prof. RNDr. Petr Štěpnička, Ph.D., DSc. Abstract: The aim of this diploma thesis is the preparation of coordination compounds containing ferrocene phosphinoamide FcCONHPPh2 (1, Fc = ferrocenyl), whose preparation was discussed in author's bachelor thesis. Twelve new complexes are described in this thesis, including their characterisation by NMR and infrared spectroscopy, elemental analysis and mass spectrometry. In all cases the crystal structure was determined. Two palladium(II), one rhodium(III) and one ruthenium(II) precursors were used for the preparation of the complexes with each providing three new compounds. A reaction of the precursors with phosphinoamide 1 yielded complexes, in which the phosphinoamide was P-coordinated. This compound was a precursor for the other two complexes. The first one was obtained by a reaction with silver(I) perchlorate producing a cationic P,O-chelate. The other was obtained by a reaction with potassium tert-butoxide resulting in neutral P,O- chelate. All twelve complexes were prepared with optimised yields. Keywords: ferrocene, amides, phosphines, palladium, rhodium, ruthenium, structure elucidation.
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Study of contamination of river sediments with platinum metals
Novotný, Matěj ; Řezáčová, Veronika (referee) ; Komendová, Renata (advisor)
This work deals with the characteristics of platinum metals and problems related to their toxicity and mobility in the environment, especially in the aquatic environment. These metals are released into the environment due to the use of automotive catalysts. Their function is based on the catalytic properties of platinum metals. Because of the high temperatures, these metals can be oxidized in the catalyst and subsequently emitted together with the combustion products into the surrounding atmosphere. The aim of the thesis is to measure real samples of river sediments of the river Svratka on the territory of the city of Brno and to find the possibility of contamination of the aquatic environment with these metals.
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Reactivity of transition metals - influence of the degree of oxidation of active substrate
Kettner, Miroslav ; Nehasil, Václav (advisor)
The impacts of fluorine doping of ceria are studied by means of surface science experimental methods. Fluorine-doped and fluorine-free ceria layers are epitaxially grown on rhodium single crystals and their properties are compared in regular and inverse catalyst configurations. A procedure for epitaxial growth of CeO2(110) and CeOxFy(110) layers on Rh(110) single crystal is developed and described in detail. Shape alterations of Ce 3d spectrum brought about by fluorine doping are explained and a suitable deconvolution method is proposed. Special attention is focused towards stability of fluorine in ceria. Presented data show that fluorine incorporation in ceria lattice causes stable reduction of ceria, which withstands up to 200řC in near-ambient pressure conditions. Morphological changes are observed due to elongation of surface lattice constant of reduced ceria. Oxygen storage capacities and hydrogen oxidation reaction rates of four different studied systems are compared and discussed. The twofold nature of oxygen exposure of fluorinated ceria is discovered and explained. Oxygen repels fluorine from the surface, while the remaining part of fluorine is expelled to adsorbate positions, where its electronic state is altered. Moreover, such fluorine is prone to interact with atomic hydrogen. This reaction is...
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Reactivity of transition metals - influence of the degree of oxidation of active substrate
Kettner, Miroslav ; Nehasil, Václav (advisor) ; Jiříček, Petr (referee) ; Lykhach, Yaroslava (referee)
The impacts of fluorine doping of ceria are studied by means of surface science experimental methods. Fluorine-doped and fluorine-free ceria layers are epitaxially grown on rhodium single crystals and their properties are compared in regular and inverse catalyst configurations. A procedure for epitaxial growth of CeO2(110) and CeOxFy(110) layers on Rh(110) single crystal is developed and described in detail. Shape alterations of Ce 3d spectrum brought about by fluorine doping are explained and a suitable deconvolution method is proposed. Special attention is focused towards stability of fluorine in ceria. Presented data show that fluorine incorporation in ceria lattice causes stable reduction of ceria, which withstands up to 200řC in near-ambient pressure conditions. Morphological changes are observed due to elongation of surface lattice constant of reduced ceria. Oxygen storage capacities and hydrogen oxidation reaction rates of four different studied systems are compared and discussed. The twofold nature of oxygen exposure of fluorinated ceria is discovered and explained. Oxygen repels fluorine from the surface, while the remaining part of fluorine is expelled to adsorbate positions, where its electronic state is altered. Moreover, such fluorine is prone to interact with atomic hydrogen. This reaction is...
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Study of dependence of the metal-oxide electron structure on the reactivity of these systems
Ševčíková, Klára ; Nehasil, Václav (advisor) ; Jiříček, Petr (referee) ; Plšek, Jan (referee)
The presented thesis focuses on studying the interaction between rhodium and cerium oxide and its impact on the reactivity. We investigated two different systems, Rh/CeOx and Rh-CeOx, by means of the photoelectron spectroscopy and the temperature programmed reactions. Rh/CeOx stands for rhodium nanoparticles supported by cerium oxide thin film. We show that there is an electronic metal-substrate interaction between rhodium and cerium oxide. The type of the interaction depends on a degree of cerium oxide reduction and it has a tremendous impact on the reactivity of the system. On the other hand, Rh-CeOx represents cerium oxide thin films doped by rhodium. We characterized the properties of the films with various concentration of rhodium. We show that the morphology, chemical composition and reactivity of the samples strongly depend on the concentration of the rhodium dopant. Powered by TCPDF (www.tcpdf.org)
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Study of dependence of the metal-oxide electron structure on the reactivity of these systems
Ševčíková, Klára
Title: Study of dependence of the metal-oxide electron structure on the reactivity of these systems Author: Klára Ševčíková Supervisor: doc. RNDr. Václav Nehasil, Dr., Department of Surface and Plasma Science Abstract The presented thesis focuses on studying the interaction between rhodium and cerium oxide and its impact on the reactivity. We investigated two different systems, Rh/CeOx and Rh- CeOx, by means of the photoelectron spectroscopy and the temperature programmed reactions. Rh/CeOx stands for rhodium nanoparticles supported by cerium oxide thin film. We show that there is an electronic metal-substrate interaction between rhodium and cerium oxide. The type of the interaction depends on a degree of cerium oxide reduction and it has a tremendous impact on the reactivity of the system. On the other hand, Rh-CeOx represents cerium oxide thin films doped by rhodium. We characterized the properties of the films with various concentration of rhodium. We show that the morphology, chemical composition and reactivity of the samples strongly depend on the concentration of the rhodium dopant.
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Computational Study of the Properties and Reactivity of Bioinroganic Transition Metal Complexes
Baxová, Katarína ; Burda, Jaroslav (advisor) ; Sochorová Vokáčová, Zuzana (referee)
This work is focused on the reactions of diaqua-tetrakis(μ-acetylato)dirhodium(II,II) with guanine, that shows anti-cancer activities. Guanine can bond to the complex either by oxygen O6 or by nitrogen N7. We studied three possible versions of the system - one that is protonated on guanine, one protonated on the paddle-wheel and a neutral one. For all 6 reactions transition structures were found. For reactants, tranzition states and products we computed the values of electron density in the critical points of bonds, partial atom charges and the interaction energies of the system, guanine and water on the b3lyp/aug-cc- pvdz level. Pseudobasis and pseudopotentials were employed in the case of rhodium atom. For all the reactions thermodynamical properties were computed. Powered by TCPDF (www.tcpdf.org)
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