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Part 1, Arene oxidation with 2,6-dichloropyridine N-oxide catalyzed by ruthenium porphyrins: Part 2, Imine complexes of ruthenium and manganese with acyclic tetradentate N₂O₂-donors as oxidation catalysts for styrene oxidation. / Arene oxidation with 2,6-dichloropyridine N-oxide catalyzed by ruthenium porphyrins / Imine complexes of ruthenium and manganese with acyclic tetradentate N₂O₂-donors as oxidation catalysts for styrene oxidation

by Lo Tim Lun. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1998. / Includes bibliographical references (leaves 68-71). / Abstract also in Chinese. / Acknowledgments --- p.i / Abstract --- p.ii / Abbreviations --- p.iii / Table of Contents --- p.iv / Chapter Part 1. --- "Arene Oxidation with 2,6-Dichloropyridine- N-oxide Catalyzed by Ruthenium Porphyrins" --- p.1 / Chapter 1. --- Introduction --- p.1 / Chapter 1.1 --- Natural Occurrence of Cytochrome P-450 --- p.1 / Chapter 1.2 --- Biomimetic Models of Cytochromes of P-450 --- p.4 / Chapter 1.3 --- Homogenous Metalloporphyin Catalyzed Oxidation Mimicking Cytochrome P-450 --- p.5 / Chapter 1.4 --- Synthetic Porphyrin Revolution: Third Generation of Porphyrins --- p.6 / Chapter 1.5 --- Fourth-Generation of Porphyrins --- p.9 / Chapter 1.6 --- Variation of Oxygen Donors and Bound Transition Metals --- p.11 / Chapter 1.7 --- Objective --- p.12 / Chapter 2. --- Results and Discussion --- p.15 / Chapter 2.1 --- Synthesis of β-tetraaryl Substituted Mesitylporphyrin and their Ruthenium Carbonyl Complexes --- p.15 / Chapter 2.2 --- "Oxidation of Aromatic Compounds Catalyzed by Ruthenium Porphyrins in 2,6-Dichloropyridine N-oxide System" --- p.17 / Chapter 2.3 --- "Synthesis of trans-Dichloro-tetrakis(p-chlorophenyl)- tetramesitylporphyrinato Ruthenium(IV) Complex, trans- RuTMP(p-ClPh)4(Cl2)" --- p.21 / Chapter 2.4 --- "Oxidation of Aromatic Compounds Catalyzed by trans- Ru(TMP)(p-ClPh)4(Cl2) with 2,6-Dichloropyridine N- oxide" --- p.24 / Chapter 2.5 --- "Effect of Additives to the Catalytic Oxidation of Aromatic Compound by Ru(por)-2,6-Dichloropyridine N- oxide" --- p.24 / Chapter 2.6 --- "Effect of Lewis Acids on the Catalytic Oxidation of Aromatic Compound by Ru(por)-2,6-Dichloropyridine N- oxide" --- p.27 / Chapter 3. --- Conclusion --- p.29 / Chapter 4. --- Experimental Section --- p.30 / Chapter 5. --- Reference --- p.39 / Chapter Part 2. --- Imine Complexes of Ruthenium and Manganese with Acyclic Tetradenate N202-Donors as Oxidation Catalysts for Styrene Epoxidation --- p.42 / Chapter 1 --- Introduction --- p.42 / Chapter 1.1 --- Salen-type Metal Complexes with N202 Anionic Donor Set --- p.43 / Chapter 1.2 --- High-valent Ruthenium Complexes with π-Aromatic Imine Ligand --- p.45 / Chapter 1.3 --- Objective --- p.47 / Chapter 1.3.1 --- Metal Complexes of Phenanthroline-π-aromatized Imlne --- p.47 / Chapter 1.3.2 --- Ruthenium Complex of Jacobsen Ligand --- p.48 / Chapter 2 --- Results and Discussion --- p.50 / Chapter 2.1 --- "Synthesis of cis-Dicarbonyl-[(R,R)-N, N,-bis(3,5-di-tert- butylsalcylidene)-1,2-cyclohexanediaminato (2-)] Ruthenium(II) Complex" --- p.50 / Chapter 2.2 --- "Synthesis of 2,9-Bis(3,5-di-tert-butyl-2-hydroxyphenyl)- 1,10-phenanthroline and Its Manganese and Ruthenium Complexes" --- p.55 / Chapter 2.3 --- Epoxidation of Styrene Catalyzed by Manganese and Ruthenium Phenanthroline Complexes with Hyprochlorite as Oxidant in Different pH Media --- p.58 / Chapter 3. --- Conclusion --- p.60 / Chapter 4. --- Experimental Section --- p.61 / Chapter 5. --- Reference --- p.69 / Appendix --- p.73 / NMR Spectra --- p.78

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_322180
Date January 1998
ContributorsLo, Tim Lun., Chinese University of Hong Kong Graduate School. Division of Chemistry.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, bibliography
Formatprint, v, 91 leaves : ill. ; 30 cm.
RightsUse of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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