Synthèses et caractérisations de nouveaux complexes à base de ruthénium (II) à ligands polypyridinique et carbène N-hétérocyclique

Synthèses et caractérisations de nouveaux complexes à base de ruthénium (II) à ligands polypyridinique et carbène N-hétérocyclique PDF Author: Mohamed Dakkach
Publisher:
ISBN:
Category :
Languages : fr
Pages : 261

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Ruthenium-N-Heterocyclic Carbene and Ruthenium Acetylide Complexes Supported by Macrocyclic Porphyrin Or Tetradentate Schiff Base Ligands

Ruthenium-N-Heterocyclic Carbene and Ruthenium Acetylide Complexes Supported by Macrocyclic Porphyrin Or Tetradentate Schiff Base Ligands PDF Author: Ka-Ho Chan
Publisher: Open Dissertation Press
ISBN: 9781361379714
Category :
Languages : en
Pages :

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This dissertation, "Ruthenium-N-heterocyclic Carbene and Ruthenium Acetylide Complexes Supported by Macrocyclic Porphyrin or Tetradentate Schiff Base Ligands: Synthesis, Structure and Catalytic Applications" by Ka-ho, Chan, 陳嘉豪, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. Abstract: Abstract of thesis entitled RUTHENIUM-N-HETEROCYCLIC CARBENE AND RUTHENIUM ACETYLIDE COMPLEXES SUPPORTED BY MACROCYCLIC PORPHYRIN OR TETRADENTATE SCHIFF BASE LIGANDS: SYNTHESIS, STRUCTURE AND CATALYTIC APPLICATIONS Submitted by Chan Ka Ho for the degree of Doctor of Philosophy at The University of Hong Kong in March 2015 Transition metal-catalyzed C-C and C-N bond formation reactions are important transformations in synthetic organic chemistry. In the endeavor of this thesis to develop robust/versatile catalysts for these reactions, the trans effect imposed by N-heterocyclic carbene (NHC) and acetylide ligand onto ruthenium complexes supported by macrocyclic porphyrin or tetradentate Schiff-base ligands was studied. The catalytic activity of these novel ruthenium complexes towards carbene and/or nitrene transfer and insertion reactions was also explored. II A series of bis(NHC)ruthenium(II) porphyrin complexes [Ru (Por)(NHC) ] were synthesized by deprotonation of imidazolium salt using a strong base. These complexes displayed unprecedentedly high catalytic activity towards carbene/nitrene transfer and insertion reactions, including alkene cyclopropanation and aziridination, carbene C-H, S-H, N-H and O-H insertions, and nitrene C-H insertion with product -1 turnover frequency up to 1950 min . Carbene modification of N-terminus of peptide o II at 37 C was achieved. Chiral [Ru (D -Por)(NHC) ] catalyst led to highly 4 2 enantioselective carbene/nitrene transfer and insertion reactions with up to 98% ee. DFT calculations revealed that the strong σ-donor strength of trans axial NHC ligand stabilizes the formation of metal-carbene and metal-nitrene intermediate from decomposition of diazo compounds and organic azides, which is crucial for the transition metal-catalyzed oxidative C-C and C-N bond formation reactions to proceed under mild reaction conditions. II A series of ruthenium Schiff-base complexes cis-β-[Ru (Schiff-base)(CO) ] were synthesized and characterized. These complexes showed high catalytic activity towards enantioselective cyclopropanation, carbene C-H and Si-H bond insertions. II t The cis-[Ru (2-CPh -4- Bu-Schiff-base)(CO) ]-catalyzed intermolecular 3 2 cyclopropanation of styrene with EDA in CH Cl afforded desired cyclopropane 2 2 product in 90% isolated yield and 95% ee with a product turnover number of 9000. Excellent trans- and high enantioselectivity were observed with wide substrate scope, including conjugated, electron-rich, electron-deficient and aliphatic terminal alkenes. Carbene C-H and Si-H insertion reactions proceeded smoothly with II t cis-[Ru (2-CPh -4- Bu-Schiff-base)(CO) ] as catalyst, giving the desired products in 3 2 82-97% yields with excellent enantioselectivity (up to 99% ee). The same complex was also catalytically active towards intramolecular cyclopropanation and intramolecular alkyl carbene sp C-H bond insertion to give cis-products with up to 99:1 cis: trans ratio and with excellent enantioselectivities (up to 98% ee). DFT calculations on the intermolecular cyclopropanation catalyzed by II cis-β-[Ru (Schiff-base)(CO) ] revealed that among the ruthenium-carbene intermediates possibly involved in the reactions, the cis-β species are more stable than their trans isomer with

Synthesis of Ruthenium Complexes Having One Or More N-heterocyclic Carbene Ligands Supported on Hybrid Mesostructured Silicas and Their Use in the Hydrogenation of Carbon Dioxide

Synthesis of Ruthenium Complexes Having One Or More N-heterocyclic Carbene Ligands Supported on Hybrid Mesostructured Silicas and Their Use in the Hydrogenation of Carbon Dioxide PDF Author: Mathieu Baffert
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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The goal of this PhD was to elaborate supported Ru-NHC catalytic materials based on hybrid organic-inorganic materials having imidazolium units perfectly distributed within a silica matrix. Passivation of these imidazolium materials followed by formation of NHC-carbene and reaction with [RuCl2(p-cymene)]2 provided these well-defined surface sites of general structures RuCl2(NHC)(L), where L was para-cymene (p-cymene) or THF depending on the reaction conditions, which could be further replaced by PMe3. These systems were then tested in the hydrogenation of CO2 in presence of amine to give formamides. The mono-NHC systems were highly active only in the presence of PMe3 ligands, but suffered from Ru leaching, evidencing the low stability of the NHC-Ru bond under the reaction conditions. On the other hand, dinuclear bis-NHC Ru systems were also developed, and they displayed much improved activity and stability in the hydrogenation of CO2 in the presence of PMe3 compared to the mono-NHC systems. This allowed the use of much higher reaction temperatures (200 °C) and provided heterogeneous catalysts with performances close to those obtained with the best homogeneous catalysts, Cl2Ru(dppe)2.

Syntheses, Spectroscopy and Photophysics of Ruthenium(ii) Carbene Complexes and Diimine Complexes with Functionalized Ligands for Molecular Recognition and Organized Assembly

Syntheses, Spectroscopy and Photophysics of Ruthenium(ii) Carbene Complexes and Diimine Complexes with Functionalized Ligands for Molecular Recognition and Organized Assembly PDF Author: Wai-Kin Chu
Publisher:
ISBN: 9781374785373
Category :
Languages : en
Pages :

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Ruthenium-N-heterocyclic Carbene and Ruthenium Acetylide Complexes Supported by Macrocyclic Porphyrin Or Tetradentate Schiff Base Ligands

Ruthenium-N-heterocyclic Carbene and Ruthenium Acetylide Complexes Supported by Macrocyclic Porphyrin Or Tetradentate Schiff Base Ligands PDF Author:
Publisher:
ISBN:
Category : Organoruthenium compounds
Languages : en
Pages : 468

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Syntheses, Spectroscopy and Photophysics of Ruthenium(II) Carbene Complexes and Diimine Complexes with Functionalized Ligands for Molecular Recognition and Organized Assembly

Syntheses, Spectroscopy and Photophysics of Ruthenium(II) Carbene Complexes and Diimine Complexes with Functionalized Ligands for Molecular Recognition and Organized Assembly PDF Author: Wai-kin Chu (Ph.D.)
Publisher:
ISBN:
Category : Carbenes (Methylene compounds)
Languages : en
Pages : 652

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Half-sandwich Complexes of Ruthenium Supported by N-Heterocyclic Carbene Ligands

Half-sandwich Complexes of Ruthenium Supported by N-Heterocyclic Carbene Ligands PDF Author: Van Hung Mai
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Category :
Languages : en
Pages :

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This thesis presents the preparation and catalytic reactivity of novel half-sandwich ruthenium complexes supported by N-Heterocyclic Carbene (NHC) ligands. The cationic half-sandwich ruthenium complexes [Cp(IPr)Ru(CH3CN)2]+ show interesting reactivities toward the transfer hydrogenation of different unsaturated substrates, such as ketones, olefins, N-heterocycles, and nitriles. Kinetic studies disclose that a neutral trishydride ruthenium complex is actually involved in the catalytic cycle, playing the role as a resting state. Further investigations on the sub-class of trishydride ruthenium complexes bearing NHC ligands (Cp'(NHC)RuH3) reveal that these complexes have an unusual and great catalytic performance toward the hydrodefluorination (HDF) of fluorinated aromatic and aliphatic compounds. The combined kinetic studies, cross-over experiments and rate law analysis suggest an unusual mechanistic pathway for the Cp*(IPr)RuH3 catalyzed HDF. This study is one of the rare examples where isopropanol is employed as a reducing agent for the metal-mediated HDF reaction. A class of silyl dihydride ruthenium complexes, derived from Cp(IPr)RuH3 are prepared. These silyl hydrido derivatives are great compounds for the study of the inter ligand hypervalent interaction (IHI), an interesting phenomenon for many non-classical silane complexes. This study also suggests that the replacement of phosphines by their isolobally analogous NHC ligands result in stronger IHI interactions in the corresponding compounds. Another type of non-classical interaction was systematically scrutinized in a ii series of new cationic and neutral silane sigma complexes of ruthenium bearing different silyl moieties. These new NHC-supported ruthenium complexes allow for direct comparation with the known phosphine analogues, which reveals interplay of steric and electronic factors on the extent of Si-H complexation to metal and the extent of additional interligand interactions between Ru-Cl and chlorosilane ligand. Finally, new trishydride ruthenium complexes bearing NHC ligands (Cp'(NHC)RuH3) catalyze the H/D exchange reaction of various N-heterocycle substrates; their catalytic performance can be considered as one of the mildest, and most efficient approaches.

Synthesis and Characterization of a New Class of Mixed Ligand Ruthenium Complexes Containing 2,2'-bipyridine and 3,3'-dimetheyl-1,1'-methylenebisimidazolium Carbene Ligands

Synthesis and Characterization of a New Class of Mixed Ligand Ruthenium Complexes Containing 2,2'-bipyridine and 3,3'-dimetheyl-1,1'-methylenebisimidazolium Carbene Ligands PDF Author: Ryan Mahabir
Publisher:
ISBN:
Category :
Languages : en
Pages : 200

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Ruthenium Complexes

Ruthenium Complexes PDF Author: Alvin A. Holder
Publisher: John Wiley & Sons
ISBN: 3527695206
Category : Science
Languages : en
Pages : 347

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Edited by a team of highly respected researchers combining their expertise in chemistry, physics, and medicine, this book focuses on the use of rutheniumcontaining complexes in artificial photosynthesis and medicine. Following a brief introduction to the basic coordination chemistry of ruthenium complexes and their synthesis in section one, as well as their photophysical and photochemical properties, the authors discuss in detail the major concepts of artificial photosynthesis and mechanisms of hydrogen production and water oxidation with ruthenium in section two. The third section of the text covers biological properties and important medical applications of ruthenium complexes as therapeutic agents or in diagnostic imaging. Aimed at stimulating research in this active field, this is an invaluable information source for researchers in academia, health research institutes and governmental departments working in the field of organometallic chemistry, green and sustainable chemistry as well as medicine/drug discovery, while equally serving as a useful reference also for scientists in industry.

Synthesis and Characterization of Ruthenium (II) Polypyridyl Complexes

Synthesis and Characterization of Ruthenium (II) Polypyridyl Complexes PDF Author: Youxiang Wang
Publisher:
ISBN:
Category : Diazo compounds
Languages : en
Pages : 190

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