Download or read book Synthesis Characterisation and Catalytic Activity of Gold Rhodium and Palladium Complexes Featuring Fluorinated N heterocyclic Carbene Ligands written by Mohamad Shazwan Shah Bin Jamil and published by . This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Palladium and Gold N heterocyclic Carbene Complexes written by Caroline Magdalene Zinser and published by . This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book N Heterocyclic and Mesoionic Carbene Complexes of Rhodium and Palladium written by and published by . This book was released on 2015 with total page 584 pages. Available in PDF, EPUB and Kindle. Book excerpt: Dimeric rhodium N-heterocyclic carbene (NHC) complexes [Rh(NHC)(C2H4)Cl]2 react with a variety of other neutral donors to form heteroleptic complexes [(L)Rh(NHC)(C2H4)Cl] (L = phosphine, pyridine) or [(L)Rh(NHC)Cl] (L = 2,2'-bipyridine (bipy), 1,10-phenanthroline (phen)). The reactivity of the resulting complexes towards O2 was investigated. In particular, [(bipy)Rh(NHC)Cl] and [(phen)Rh(NHC)Cl] resulted in RhIII peroxo complexes. In contrast, [Rh(NHC)2(O2)Cl] display particularly short O-O bond lengths and are described as singlet oxygen species. Interestingly, the mode in which O2 binds is associated with the coordination number about the transition metal complex, which is related to its reducing power. [Rh(IPr)(C2H4)Cl]2 reacts with phenyl pyridine derivatives at room temperature resulting in formal C-H activations. Upon the treatment of phenyl pyridine with pinacol borane (HBPin) in the presence of a weak base and a catalytic amount of [Rh(IPr)(C2H4)Cl]2, C-H borylated products were obtained in high yield and selectivity. The borylated products can then be used as substrates in the palladium catalyzed Suzuki-Miyaura cross coupling with aryl halides. 1,2,3-Triazole mesoionic carbene (tMIC) ligands were generated upon treatment of corresponding triazolium salts with strong bases, and can be trapped in the presence of a transition metal. The synthesis of Ag-tMIC complexes proceeds by a facile and mild route upon treatment of the triazolium salt with Ag2O. The resulting Ag-tMIC complexes undergo facile transmetallation to both Pd and Rh under very mild conditions resulting in air and moisture stable metal complexes. Triazolium salts can further be metallated to Pd in the presence of weak bases, and the resulting Pd-tMIC complexes are active catalysts in the Mizoroki-Heck reaction with aryl iodides. Benzylic trifluoromethyl sulfones are competent electrophilic substrates in palladium catalyzed cross coupling reactions, resulting in the formation of triarylmethanes in high yields under mild conditions. These substrates are conveniently synthesized and are highly reactive starting materials with phenyl boronic acids in the presence of a Pd-NHC catalyst. The structure of the Pd-NHC precatalyst is crucial, as only [(NHC)Pd(allyl)Cl] type complexes appear to be effective. These complexes can be conveniently synthesized upon the treatment of the corresponding imidazolium salt with a strong base and [Pd(allyl)Cl]2.
Download or read book Synthesis of Novel N heterocyclic Carbene palladium Complexes and Their Catalytic Activity written by Daniel P. Guest and published by . This book was released on 2017 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis and Application of Rhodium I Fischer Carbene Complexes written by Granny Kabelo Ramollo and published by . This book was released on 2016 with total page 250 pages. Available in PDF, EPUB and Kindle. Book excerpt: In this study, novel rhodium(I) carbene complexes were synthesized and fully characterized via a carbene ligand transfer methodology from Group 6 Fischer carbene complex precursors and subsequent ligand modification. The classic Fischer route was followed towards the isolation of mono- and biscarbene complexes of the form [M(CO)5{C(OR)R'}] [M = Cr, W; R = Me, Et; R' = 2-furyl, 2-thienyl, ferrocenyl] (complexes 1 6, 9 and 10), and [M(CO)5?{C(OR)-R''-C(OR)}M(CO)5] [M = Cr; R = Me, Et; R'' = 2,2'-bithien-5,5'-diyl, 2,5-furadiyl, 1,1'-ferrocendiyl] (complexes 7, 8 and 11), respectively. Analogous aminocarbene complexes [M(CO)5{C(NH2)R'}] [M = Cr, W; R' = 2-thienyl, ferrocenyl) (complexes 12 and 13) were prepared by simple aminolyses of the alkoxycarbene complex precursors and all isolated products were characterized using NMR and FT-IR spectroscopic methods, the results of which were comparable with literature values. Transmetallation techniques were employed in an attempt to transfer the carbene ligands to a rhodium(I) metal center of the dimeric [Rh(cod)Cl]2 precursor to result in novel 2-furyl, 2-thienyl and ferrocenyl Fischer carbene complexes of rhodium(I). Only the ferrocenylcarbene complex 15 [Rh(cod)Cl{C(OEt)Fc) were found to be stable enough to isolate, as the heteroaryl (thienyl, furyl) substituted carbene ligands dissociated in solution, with resultant decomposition dimerization to form the corresponding alkene and starting [Rh(cod)Cl]2 complex, as indicated by NMR spectroscopy. The ferrocenylcarbene complex 15 was then employed as a precursor for the syntheses of all other rhodium(I) carbene complexes via cod ligand substitution and aminolysis reactions to isolate mono- and dicarbonylcarbene complexes 16 23, [Rh(LL)Cl{C(X)Fc}] [LL = cod, (CO)2, (CO, PPh3), (CO, PCy3), (CO, P(OPh3)), (CO, AsPh3); X = OEt,NHnPr], with variable ?-acceptor properties. Full characterization of the novel complexes were achieved by single crystal XRD and spectroscopic methods. From the FT-IR data collected, the donor ability of the electronic environment around the rhodium(I) center was found to correlate with the known electron-donor ability of the coligands in the order PCy3>PPh3,AsPh3>P(OPh)3. This trend was corroborated by cyclic voltammetric methods through which the electron-withdrawing effects of the coligands were studied, and it was confirmed that the cod ligand is the most electrondonating whilst the dicarbonyls were found to be the least donating in the series. In addition, the increased electron donation of the aminocarbene ligands compared to the ethoxycarbene ligands was found to significantly influence the redox potentials of the metal centre in the studied complexes. The isolated rhodium(I) Fischer carbene complexes 15 - 22 were screened as catalyst precursors for the hydroformylation of 1-octene. Good to excellent catalytic activities, with selectivity toward the formation of the linear nonanal, was observed. These results were found to be comparable to results reported for rhodium(I) N-heterocyclic carbene complexes. A mercury-drop test was done to exclude a heterogeneous catalytic mode of action. Finally, the stability of the catalyst precursor 15 (and 17) was probed by an NMR experiment carried out under hydroformylation conditions. The Rh-Ccarbene bond is retained, although the presumed catalytically active species, the rhodium carbene carbonyl hydride complex could not be identified.
Download or read book Design Synthesis and Catalytic Activity of Di i N i Heterocyclic Carbene Complexes of Nickel and Palladium written by and published by . This book was released on 2008 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Rhodium and Iridium Complexes Supported by Chelating Bis N heterocyclic Carbene Ligands written by Roxy Joanne Lowry and published by . This book was released on 2009 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: ABSTRACT: Eighty-five percent of all industrial chemical processes occur catalytically. The world's expanding appetite for mass production of exotic chemicals necessitates the design and application of enhanced catalysts. To optimize catalytic materials, the detailed relationships between catalyst architecture and reactivity must be determined. Although for many ligand families these relationships are well understood, novel catalysts require in depth empirical investigation to determine these connections. The design of a novel di-N-heterocyclic carbene family of ligands in reported herein. These C2 symmetric ligands are based on the rigid 9,10-dihydro-9,10-ethanoanthracene backbone and designed for utilization in chiral catalysis. Thorough investigation into the relationships between the ligand's structure and the architecture of the resulting rhodium and iridium catalysts directed the design of three generations of our novel ligand family. The first generation, trans-1,1'-[9,10-dihydro-9,10-ethanoanthracene-11,12- diyldimethanediyl]bis(benzylimidazole) bis(triflouromethansulfonate) [DEAM-BI](OTf)2 (2-1), is too flexible to enforce a rigid chiral pocket about a metal center under catalytic conditions. The constrained second generation ligands, trans-1,1'-(9,10-dihydro-9,10-ethanoanthracene.
Download or read book The Organometallic Chemistry of N heterocyclic Carbenes written by Han Vinh Huynh and published by John Wiley & Sons. This book was released on 2017-02-03 with total page 352 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Organometallic Chemistry of N-heterocyclic Carbenes describes various aspects of N-heterocyclic Carbenes (NHCs) and their transition metal complexes at an entry level suitable for advanced undergraduate students and above. The book starts with a historical overview on the quest for carbenes and their complexes. Subsequently, unique properties, reactivities and nomenclature of the four classical NHCs derived from imidazoline, imidazole, benzimidazole and 1,2,4-triazole are elaborated. General and historically relevant synthetic aspects for NHCs, their precursors and complexes are then explained. The book continues with coverage on the preparation and characteristics of selected NHC complexes containing the most common metals in this area, i.e. Ni, Pd, Pt, Ag, Cu, Au, Ru, Rh and Ir. The book concludes with an overview and outlook on the development of various non-classical NHCs beyond the four classical types. Topics covered include: Stabilization, dimerization and decomposition of NHCs Stereoelectronic properties of NHCs and their evaluation Diversity of NHCs Isomers of NHC complexes and their identification NMR spectroscopic signatures of NHC complexes normal, abnormal and mesoionic NHCs The Organometallic Chemistry of N-heterocyclic Carbenes is an essential resource for all students and researchers interested in this increasingly important and popular field of research.
Download or read book Rhodium iii Complexes Containing C4 bound N heterocyclic Carbenes Synthesis Coordination Chemistry and Catalytic Activity in Transfer Hydrogenation written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis of Palladium II N heterocyclic Carbene Via Transmetaliation of Silver I Complex and Its Catalytic Activity in Epoxidation of Alkene written by Ghani Ur Rehman and published by . This book was released on 2014 with total page 133 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis Reactivity and Catalytic Applications of Ruthenium and Palladium Complexes Supported by New Pincer Ligands written by Morgan C. MacInnis and published by . This book was released on 2011 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: ABSTRACT continued: These transfer hydrogenation studies are among the first catalytic studies of silyl-pincer complexes and establish [R-PSiP]M species as viable candidates for catalysis. The synthesis and reactivity of 4- and 5-coordinate RuII complexes featuring the [Cy-PSiP] ligand were explored. Reaction of [Cy-PSiP]H with [(p-cymene)RuCl2]2 in the presence of NEt3 and PCy3 resulted in the formation of ([Cy-PSiP]RuCl)2, which serves as a precursor to a series of unprecedented 4-coordinate, formally 14-electron [Cy-PSiP]RuX (X = NHAr, N(SiMe3)2, OtBu) complexes that feature an unusual trigonal pyramidal geometry at Ru. The reactivity of these novel diamagnetic complexes is described, including the reaction of [Cy-PSiP]RuOtBu with amine-boranes resulting in the formation of rare bis(?-BH) complexes. Computational studies confirmed the key role of the strongly ?-donating silyl group of the Cy-PSiP ligand in facilitating the synthesis of such low-coordinate Ru species and enforcing the unusual trigonal pyramidal geometry. The mechanism of ammonia-borane activation was also examined computationally. Lastly, the synthesis and structural characterization of PdII complexes supported by the pincer-like bis(amino)phosphido ligand [?3-(2-Me2NC6H4)2P]- ([NPN]) is described. Examples of ?1-, ?2-, and ?3-NPN coordination to Pd are described, as is the catalytic activity of ([NPN]PdX)2 (X = Cl, OAc, OTf) complexes in the Heck olefin arylation reaction. In an effort to discourage the formation of phosphido-bridged dinuclear complexes, pre-coordination of the Lewis acid BPh3 to [NPN] was pursued. Upon reaction of [N(P?BPh3)N]K with [PdCl(C3H5)]2, the ?1-allyl complex [?3-N(P?BPh3)N]Pd(?1-C3H5) was isolated, which establishes the coordination of a Lewis acid to the phosphido donor of the [NPN] ligand as a viable strategy for encouraging the formation of mononuclear ?3-NPN complexes.
Download or read book Synergism Between N heterocyclic Carbene and Phosphorus based Ligands in Ruthenium and Palladium Catalytic Systems written by Thibault Édouard Schmid and published by . This book was released on 2013 with total page 286 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Design Synthesis and Catalytic Activity of Di i N i Heterocyclic Carbene Complexes of Nickel and Palladium written by and published by . This book was released on 2009 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Gold Catalysis written by Laura Prati and published by CRC Press. This book was released on 2016-01-05 with total page 521 pages. Available in PDF, EPUB and Kindle. Book excerpt: Since the first report on alcohol oxidation in 1998, many studies have highlighted some peculiarity of gold with respect to other metals. Some analogies have been found between gas and liquid phases, but the big challenge to operate in a condensed phase lies in the role of the solvent in tuning the reactant-catalyst contact. Liquid-phase oxidation
Download or read book Rhodium Catalyzed Hydroformylation written by Piet W.N.M. van Leeuwen and published by Springer Science & Business Media. This book was released on 2006-04-11 with total page 291 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Download or read book Supported Molecular Rhodium Complexes and Dimers written by Dicle Yardimci and published by . This book was released on 2013 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Solid catalysts incorporating transition metals are important in industry, providing cost- effective syntheses, ease of separation from products, and control of selectivity. The metal is often expensive and thus often constitutes only about one percent of the catalyst mass, being highly dispersed on a high-area support. Dispersed metals in industrial catalysts are usually highly nonuniform in structure and challenging to characterize, and consequently relationships between structure and catalyst performance are typically less than fully understood. Our approach to the investigation of supported metal catalysts involves the synthesis of uniform catalytic sites that have essentially molecular character. Supported molecular catalysts can be characterized spectroscopically to provide fundamental understanding of the catalyst structure under reactive atmospheres, and thereby determination of structural changes of working catalysts that can be correlated with the catalytic activity and selectivity. The sample characterization techniques used in this work included infrared (IR), extended X-ray absorption fine structure (EXAFS), and X-ray absorption near edge structure (XANES) spectroscopies, as well as gas chromatography (GC) and mass spectrometry (MS) to characterize reaction products. The catalysts were prepared from the organometallic precursor Rh(C2H4)2(C5H7O2) and the supports MgO and zeolite HY. These catalysts initially incorporated site-isolated, mononuclear rhodium complexes on the supports. The complexes on MgO were treated in H2 at elevated temperatures to form the smallest supported rhodium clusters--rhodium dimers. These catalysts are essentially molecular in character and allowed tailoring of the rhodium nuclearity, the ligands bonded to the rhodium, and the rhodium-support interface. The catalysts incorporated mononuclear Rh(C2H4)2 and Rh(CO)2 complexes; dimeric rhodium clusters with ethyl ligands, and dimeric rhodium clusters with CO ligands. These were tested for the hydrogenation of ethylene. Rhodium in various forms is highly active for catalytic hydrogenation of olefins. However, rhodium has been little investigated for diene hydrogenation, because, like other noble metals in the form of supported clusters or particles, it is unselective. We postulated that new catalytic chemistry of rhodium could emerge if the catalytic species were essentially molecular so that they could be tuned by the choice of the rhodium nuclearity and ligands. Thus, we investigated the influence of the following catalyst design variables on the activity and selectivity of supported rhodium for 1,3-butadiene hydrogenation: (a) the metal nuclearity, ranging from one to several; (b) the electron-donor properties of the support (MgO vs. zeolite Y); and (c) other ligands on the rhodium, including reactive hydrocarbons (ethylene or ethyl) and CO. The data show that extremely small MgO-supported rhodium clusters that are partially carbonylated are highly active and selective for the hydrogenation of 1,3-butadiene to give n-butenes. The support, the rhodium nuclearity, and the ligands on rhodium are crucial to the catalyst selectivity, transforming a metal that is typically regarded as unselective for 1,3-butadiene hydrogenation into one that is highly selective even at high conversions. Transition metals in complexes and clusters tend to aggregate to form of more stable, bulk particles under reactive atmospheres, causing catalyst deactivation. We investigated the initial steps of the aggregation of supported metal species that were highly dispersed on MgO and zeolite HY, synthesizing samples that incorporated supported rhodium complexes bonded to ligands with different reactivities (including the support), and then spectroscopically investigated the formation of extremely small rhodium clusters in the presence of H2. The stability of the rhodium complexes and the stoichiometry of the surface-mediated transformations are regulated by the support and the other ligands bonded to the rhodium, being prompted at a lower temperature with zeolite HY than the better electron-donor MgO when the rhodium complexes incorporate ethylene ligands, but occurring more facilely on the MgO than on the zeolite when the ligands are CO. The preparation of highly uniform rhodium dimers is possible. We infer that results such as those presented here may be useful in guiding the design of stable, highly dispersed supported metal catalysts by choice of the support and other ligands on the metal.
Download or read book Palladium and Gold catalyzed Transannular 4 3 Cycloaddition Reactions written by Derek T. Craft and published by . This book was released on 2010 with total page 185 pages. Available in PDF, EPUB and Kindle. Book excerpt: Unit I, Using allene RCM reactions, 12, 14 and 16 membered furan/allene macrocycles were synthesized. Selective epoxidation reactions and Platinum catalysis were unable to initiate a successful transannular [4+3] cycloaddition reaction from the 14 member macrocycle. However, a palladium catalyst system was then tested which produced the first reported example of a transannular [4+3] cycloaddition reaction in 37% yield. Gold catalysis showed a slight improvement on the product yield but competing rearrangement and [4+2] reactions were problematic. After changing the 3C component from an allene to a propargyl acetate, the reaction was optimized from 13 and 14 membered macrocycles using gold catalysis to generate [4+3] cycloadducts in high yield. The transannular [4+3] cycloaddition methodology was then applied to synthesizing the ABCD ring structure of Cortistatin A. Unit II, A short synthesis of S-(+)-Siphonodiol was completed utilizing a strategy which took advantage of the hidden symmetry of the molecule. Key steps in the synthesis were copper mediated alkyne coupling reactions. Unit III, Two new chiral N-Heterocyclic Carbene complexes were synthesized and the structures were confirmed using x-ray analysis. These complexes were found to be useful as catalysts and showed similar reactivity to Au(I)IPr in intramolecular cyclopropanation reactions from propargyl acetate/alkene substrates.
