Rhodium(iii) Complexes Containing C4-bound N-heterocyclic Carbenes: Synthesis, Coordination Chemistry, and Catalytic Activity in Transfer Hydrogenation PDF Download
Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Rhodium(iii) Complexes Containing C4-bound N-heterocyclic Carbenes: Synthesis, Coordination Chemistry, and Catalytic Activity in Transfer Hydrogenation PDF full book. Access full book title Rhodium(iii) Complexes Containing C4-bound N-heterocyclic Carbenes: Synthesis, Coordination Chemistry, and Catalytic Activity in Transfer Hydrogenation by . Download full books in PDF and EPUB format.
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Author: Pedro J. Perez
Publisher: Academic Press
ISBN: 0128010843
Category : Science
Languages : en
Pages : 316
Get Book Here
Book Description
This book contains authoritative reviews regarding the field of Organometallic Chemistry, written by highly qualified experts within the area, and reviewed by other experts before publication. Because of this high standard, AOC is one of the most cited journals in both Organic and Inorganic Chemistry fields. - High quality of the articles - Expertise of authors - Careful editing that provides an easy-to-read material
Author: Jeremy PRAETORIUS
Publisher:
ISBN:
Category :
Languages : en
Pages :
Get Book Here
Book Description
Author: Afzal Hussain
Publisher: Springer Nature
ISBN: 3031356314
Category : Science
Languages : en
Pages : 84
Get Book Here
Book Description
This book describes the emergence and recent advances in the design and development of rhodium complexes as therapeutic agents. Different classes of anticancer rhodium complexes with particular emphasis on ligands containing nitrogen-oxygen donor atoms are presented. Anticancer rhodium complexes of N-heterocyclic carbenes are described, while half-sandwich, heterobimetallic, and multinuclear rhodium complexes are discussed. Therapeutic applications of rhodium complexes beyond cancer such as antibacterial agents or antiviral agents are also analyzed, among others. Their mechanism of action is overviewed in detail, and the authors thoroughly comment on the challenges and future outlooks of research in the development of rhodium metallodrugs. This title highlights the important research carried out in the development of therapeutic rhodium complexes and is of great interest to graduates and researchers working in the area of rhodium-based therapeutic drugs.
Author: Kai Yang Wan
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
Get Book Here
Book Description
In this thesis, the synthetic protocol for a new class of enantiopure, primary-amine tethered N-heterocyclic carbene (NHC) ligands is described. The synthesis, coordination chemistry, and applications in catalysis for three ligands from this class with general formula (S,S)/(R,R)-H2N-CHPh-CHPh-NHC (NHC = -NCHCHN(C)R, R = Me, tBu, or Mes) are reported. The imidazolium salt of these ligands can be prepared in high yield and purity from the SN1 reaction between chiral sulfamidates and the corresponding N-substituted imidazoles. The method of coordination of the NHC ligands to metals depends on the acidity of the C-H functional in the imidazolium salts. Silver and copper compounds can be prepared in high yield with the ligand to the metal ratio of 2:1 or 1:1. Ruthenium, iridium, and rhodium complexes can also be prepared via transmetallation from the silver or copper reagents, intramolecular base deprotonation, or C-H oxidative addition. Four ruthenium complexes and two iridium complexes based on these ligands were proven active for ketone hydrogenation, under relatively mild condition (50°C, 25 bar H2(g)). Three half-sandwich ruthenium compounds containing Cp (cyclopentadienyl) or Cp* (1,2,3,4,5-pentamethylcyclopentadienyl) are highly active aryl and alkyl hydrogenation catalysts with TOF (turnover frequency) up to 67 s-1, TON (turnover number) up to 104, and ee (enantiomeric excess) up to 86%. An experimental and computational study of the half-sandwich ruthenium systems suggests that the heterolytic splitting of dihydrogen over the metal-amido bond and hydride transfer from the catalyst to the substrate can both be rate-determining. An alcohol-assisted mechanism was also calculated to explain the rate enhancement when the catalysis was conducted in polar, protic solvents such as 2-PrOH. A full experimental and computational study was also performed for a Fe(P-NH-P') system. Similarly, heterolytic splitting and hydride transfer are the two most energy demanding transition states. In addition, the enantiodetermining step (EDS) of this asymmetric ketone hydrogenation catalyst was calculated, and the origins of enantioselectivity were summarized as steric repulsion, the high compressibility of the backbone, and H-bond contributed stabilization.
Author: Sarah Elizabeth Flowers
Publisher:
ISBN:
Category :
Languages : en
Pages : 134
Get Book Here
Book Description
As carbon dioxide levels continue to rise in our atmosphere, scientific interest has peaked around the capture and utilization of CO2. Not only does CO2¬¬ have the potential to be used as a C1 building block for the production of value added chemicals, but CO2 also has the potential to be used as a carbon neutral hydrogen storage material in the form of formic acid. Although catalysts for CO2 reduction exist, many of these catalysts require the use of high temperatures and pressures and are not stable for prolonged exposure to the reaction conditions. Therefore, the challenge of making robust catalysts for CO2 hydrogenation that can operate under mild conditions with high activity remains outstanding. With the goal of generating a robust and highly active CO2 hydrogenation catalyst in mind, this thesis describes the fundamental metalation chemistry of a novel tripodal bis(protic N-Heterocyclic carbene)-phosphine ligand with ruthenium precursors and the reactivity of the resulting organometallic complexes with CO2. Chapter 1 provides a brief overview of CO2¬ in the earth’s atmosphere, a glimpse at CO2 hydrogenation chemistry, and an introduction to traditional and protic N-heterocyclic carbene (PNHC) chemistry. Chapter 2 describes the synthesis and characterization of PNHC Ru complexes utilizing [Cp*RuCl]4 as the ruthenium precursor. Chapter 3 investigates the coordination chemistry and synthesis of PNHC Ru complexes stemming from [(Arene)Ru] precursors. Chapter 4 describes both stoichiometric and catalytic reactivity studies of complexes synthesized in Chapters 2 and 3 with CO2. Finally, Chapter 5 dives into an entirely new subject and discusses the crystallographic structure determination of an unprecedented In¬¬37P20¬ nanocluster.
Author: Piet W.N.M. van Leeuwen
Publisher: Springer Science & Business Media
ISBN: 0306469472
Category : Science
Languages : en
Pages : 291
Get Book Here
Book Description
In the last decade there have been numerous advances in the area of rhodium-catalyzed hydroformylation, such as highly selective catalysts of industrial importance, new insights into mechanisms of the reaction, very selective asymmetric catalysts, in situ characterization and application to organic synthesis. The views on hydroformylation which still prevail in the current textbooks have become obsolete in several respects. Therefore, it was felt timely to collect these advances in a book. The book contains a series of chapters discussing several rhodium systems arranged according to ligand type, including asymmetric ligands, a chapter on applications in organic chemistry, a chapter on modern processes and separations, and a chapter on catalyst preparation and laboratory techniques. This book concentrates on highlights, rather than a concise review mentioning all articles in just one line. The book aims at an audience of advanced students, experts in the field, and scientists from related fields. The didactic approach also makes it useful as a guide for an advanced course.
Author: Ka-Ho Chan
Publisher: Open Dissertation Press
ISBN: 9781361379714
Category :
Languages : en
Pages :
Get Book Here
Book Description
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
Author: Jay James Dunsford
Publisher:
ISBN:
Category :
Languages : en
Pages : 496
Get Book Here
Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 21
Get Book Here
Book Description
A new cationic ruthenium(II) complex, [Ru(PPh 3 )(CH 3 CN) 2 LCl]Cl·5CHCl3 {L = N-(diphenylphosphino)pyridin-2-amine} has been synthesized and structurally characterized. The complex is an efficient catalyst for the transfer hydrogenation aldehydes and ketones. It can catalyze intramolecular transfer hydrogenation.
