Sökning: "in situ IR spectroscopy"
Visar resultat 16 - 20 av 20 avhandlingar innehållade orden in situ IR spectroscopy.
16. NH3-SCR chemistry for NOx abatement: Influence of zeolite support on N2O formation & phosphorus species addition
Sammanfattning : Different lattice arrangements of Si, Al, and O atoms result in a variety of pore dimensions and zeolite channel network systems, giving rise to different physicochemical environments inside the catalyst cage. The objective of the thesis work was to understand the influence of zeolite topology on NH3-assisted SCR chemistry over CHA, MFI, and BEA frameworks, on the formation of N2O and the addition of phosphorus species to attain fundamental insight into NOx emission control. LÄS MER
17. Ruthenium-Catalyzed Hydrogen Transfer Reactions : Mechanistic Studies and Chemoenzymatic Dynamic Kinetic Resolutions
Sammanfattning : The main focus of this thesis lies on transition metal-catalyzed hydrogen transfer reactions. In the first part of the thesis, the mechanism for racemization of sec-alcohols with a ruthenium complex, Ru(CO)2Cl(η5-C5Ph5) was studied. LÄS MER
18. Imine/azo-linked microporous organic polymers : Design, synthesis and applications
Sammanfattning : Microporous organic polymers (MOPs) are porous materials. Owing to their high surface area, tunable pore sizes and high physicochemical stability, they are studied for applications including gas capture and separation and heterogeneous catalysis. In this thesis, a series of imine/azo-linked MOPs were synthesized. LÄS MER
19. Mechanistic Studies on Ruthenium-Catalyzed Hydrogen Transfer Reactions
Sammanfattning : Mechanistic studies on three different ruthenium-based catalysts have been performed. The catalysts have in common that they have been employed in hydrogen transfer reactions involving alcohols and ketones, amines and imines or both. LÄS MER
20. Dinuclear metal complexes modelling active sites of metallohydrolases
Sammanfattning : To study the active sites of dinuclear metallohydrolases new metal complexes that model these sites both in structure and function have been synthesized using two new phenol based dinucleating ligands, 2-(N-isopropyl-N-((2-pyridyl)methyl)aminomethyl)-6-(N-(carboxylmethyl)-N-((2-pyridyl)methyl)aminomethyl)-4-methylphenol (IPCPMP) and 2,6-Bis[N-(N-(carboxymethyl)-N-(pyridylmethyl)amine)methyl]-4-methylphenolate (BCPMP). Both ligands contain pyridyl, tertiary amine and carboxylate groups but in IPCPMP one carboxylate donor is exchanged for a non-coordinating group yielding an unsymmetric ligand while BCPMP is symmetric with identical sets of ligands on either side of the phenol group. LÄS MER