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Reaction intermediates in homogeneous gold catalysis
Shcherbachenko, Elena ; Roithová, Jana (advisor) ; Matoušová, Eliška (referee)
The presented master thesis is devoted to the investigation of reaction intermediates in homogeneous gold catalysis. Electrospray ionization mass spectrometry (ESI-MS) was used as the primary research technique in this study. Delayed reactant labeling was used as the main method. I have focused mainly on the hydration of 1-phenyl-1-propyne catalyzed by the gold complex [Au(IPr)(MeCN)]BF4 (IPr = 1,3-bis(2,6-di-iso-propylphenyl)imidazol-2- ylidene). I have detected two main intermediates containing one or two gold atoms, respectively (monoaurated and diaurated intermediate). I have obtained rate constants for the degradation of the reaction intermediates and their half-lives. I have derived kinetic isotope effects for the formation and the decomposition of the detected intermediates. I have shown that the kinetics of the degradation of both intermediates is identical, therefore I conclude that hydration of alkynes catalyzed by gold complex [Au(IPr)(MeCN)]BF4 proceeds most probably via neutral monoaurated intermediates. These neutral intermediates are detected by ESI-MS as protonated (monoaurated intermediate) or tagged by a second gold cation (diaurated intermediate). Key words: gold catalysis, reaction intermediates, electrospray ionization, mass spectrometry.
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Effect of silver in homogeneous gold catalysis
Motloch, Petr ; Roithová, Jana (advisor) ; Hocek, Michal (referee)
Gold catalysis has recently experienced a sustained upswing in interest from scientific community. The amount of new reactions catalysed by gold is so significant that little is known about mechanisms of most of these reactions. Research into mechanisms of (not only) gold catalysed reactions is therefore very significant area of interest and important to the continued improvement of gold catalysed reactions. Formation of cationic π-complexes is considered a first mechanistic step in reactions catalysed by gold(I). The bond dissociation energies of gas phase cationic π-complexes were investigated by mass spectrometry and theory calculations in this thesis. These complexes consisted of differently substituted unsaturated hydrocarbons (alkenes, alkynes, alkadienes and allenes) and complex cations of silver and gold containing second ligand (triphenylphosphine, acetonitrile). On the basis of the results obtained from this study, a possible origin of the "silver effect" in gold(I) catalysis is discussed. Key words catalysis, gold, silver, mass spectrometry, DFT calculations, reaction intermediates
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Reaction intermediates in homogeneous gold catalysis
Shcherbachenko, Elena ; Roithová, Jana (advisor) ; Matoušová, Eliška (referee)
The presented master thesis is devoted to the investigation of reaction intermediates in homogeneous gold catalysis. Electrospray ionization mass spectrometry (ESI-MS) was used as the primary research technique in this study. Delayed reactant labeling was used as the main method. I have focused mainly on the hydration of 1-phenyl-1-propyne catalyzed by the gold complex [Au(IPr)(MeCN)]BF4 (IPr = 1,3-bis(2,6-di-iso-propylphenyl)imidazol-2- ylidene). I have detected two main intermediates containing one or two gold atoms, respectively (monoaurated and diaurated intermediate). I have obtained rate constants for the degradation of the reaction intermediates and their half-lives. I have derived kinetic isotope effects for the formation and the decomposition of the detected intermediates. I have shown that the kinetics of the degradation of both intermediates is identical, therefore I conclude that hydration of alkynes catalyzed by gold complex [Au(IPr)(MeCN)]BF4 proceeds most probably via neutral monoaurated intermediates. These neutral intermediates are detected by ESI-MS as protonated (monoaurated intermediate) or tagged by a second gold cation (diaurated intermediate). Key words: gold catalysis, reaction intermediates, electrospray ionization, mass spectrometry.
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Effect of silver in homogeneous gold catalysis
Motloch, Petr ; Roithová, Jana (advisor) ; Hocek, Michal (referee)
Gold catalysis has recently experienced a sustained upswing in interest from scientific community. The amount of new reactions catalysed by gold is so significant that little is known about mechanisms of most of these reactions. Research into mechanisms of (not only) gold catalysed reactions is therefore very significant area of interest and important to the continued improvement of gold catalysed reactions. Formation of cationic π-complexes is considered a first mechanistic step in reactions catalysed by gold(I). The bond dissociation energies of gas phase cationic π-complexes were investigated by mass spectrometry and theory calculations in this thesis. These complexes consisted of differently substituted unsaturated hydrocarbons (alkenes, alkynes, alkadienes and allenes) and complex cations of silver and gold containing second ligand (triphenylphosphine, acetonitrile). On the basis of the results obtained from this study, a possible origin of the "silver effect" in gold(I) catalysis is discussed. Key words catalysis, gold, silver, mass spectrometry, DFT calculations, reaction intermediates
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