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Author: T. R. Cundari
Publisher:
ISBN:
Category :
Languages : en
Pages : 13
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Book Description
There is considerable impetus for identification of aqueous OM catalysts as water is the ultimate ''green'' solvent. In collaboration with researchers at Ames Lab, we investigated effective fragment and Monte Carlo techniques for aqueous-phase hydroformylation (HyF). The Rh of the HyF catalyst is weakly aquated, in contrast to the hydride of the Rh-H bond. As the insertion of the olefin C=C into Rh-H determines the linear-to-branched aldehyde ratio, it is reasonable to infer that solvent plays an important role in regiochemistry. Studies on aqueous-phase organometallic catalysis were complemented in studies of the gas-phase reaction. A Rh-carbonyl-phosphine catalyst was investigated. Two of the most important implications of this research include (a) pseudorotation among five-coordinate intermediates is significant in HyF, and (b) CO insertion is the rate-determining step. The latter is in contrast to experimental deductions, highlighting the need for more accurate modeling. To this end, we undertook studies of (a) experimentally relevant PR{sub 3} co-ligands (PMe{sub 3}, PPh{sub 3}, P(p-PhSO{sub 3{sup -}}){sub 3}, etc.), and (b) HyF of propene. For the propylene research, simulations indicated that the linear: branched aldehyde ratio (linear is more desirable) is determined by thermodynamic discrimination of two distinct pathways. Other projects include a theory-experiment study of C-H activation by early transition metal systems, which establishes that weakly-bound adducts play a key role in activity selectivity. By extension, more selective catalysts for functionalization of methane (major component of natural gas) will require better understanding of these adducts, which are greatly affected by steric interactions with the ligands. In the de novo design of Tc complexes, we constructed (and are now testing) a coupled quantum mechanics-molecular mechanics protocol. Initial research shows it to be capable of accurately predicting structure ''from scratch.'' Challenges include conformational, geometric, coordination, spin, and particularly linkage (e.g., Tc-SCN versus Tc-NCS) isomerism. In general, our protocol can rapidly (
Author: T. R. Cundari
Publisher:
ISBN:
Category :
Languages : en
Pages : 13
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Book Description
There is considerable impetus for identification of aqueous OM catalysts as water is the ultimate ''green'' solvent. In collaboration with researchers at Ames Lab, we investigated effective fragment and Monte Carlo techniques for aqueous-phase hydroformylation (HyF). The Rh of the HyF catalyst is weakly aquated, in contrast to the hydride of the Rh-H bond. As the insertion of the olefin C=C into Rh-H determines the linear-to-branched aldehyde ratio, it is reasonable to infer that solvent plays an important role in regiochemistry. Studies on aqueous-phase organometallic catalysis were complemented in studies of the gas-phase reaction. A Rh-carbonyl-phosphine catalyst was investigated. Two of the most important implications of this research include (a) pseudorotation among five-coordinate intermediates is significant in HyF, and (b) CO insertion is the rate-determining step. The latter is in contrast to experimental deductions, highlighting the need for more accurate modeling. To this end, we undertook studies of (a) experimentally relevant PR{sub 3} co-ligands (PMe{sub 3}, PPh{sub 3}, P(p-PhSO{sub 3{sup -}}){sub 3}, etc.), and (b) HyF of propene. For the propylene research, simulations indicated that the linear: branched aldehyde ratio (linear is more desirable) is determined by thermodynamic discrimination of two distinct pathways. Other projects include a theory-experiment study of C-H activation by early transition metal systems, which establishes that weakly-bound adducts play a key role in activity selectivity. By extension, more selective catalysts for functionalization of methane (major component of natural gas) will require better understanding of these adducts, which are greatly affected by steric interactions with the ligands. In the de novo design of Tc complexes, we constructed (and are now testing) a coupled quantum mechanics-molecular mechanics protocol. Initial research shows it to be capable of accurately predicting structure ''from scratch.'' Challenges include conformational, geometric, coordination, spin, and particularly linkage (e.g., Tc-SCN versus Tc-NCS) isomerism. In general, our protocol can rapidly (
Author: Ewa Broclawik
Publisher: Springer
ISBN: 3030117146
Category : Science
Languages : en
Pages : 532
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Book Description
This book focuses on the electronic properties of transition metals in coordination environments. These properties are responsible for the unique and intricate activity of transition metal sites in bio- and inorganic catalysis, but also pose challenges for both theoretical and experimental studies. Written by an international group of recognized experts, the book reviews recent advances in computational modeling and discusses their interplay using experiments. It covers a broad range of topics, including advanced computational methods for transition metal systems; spectroscopic, electrochemical and catalytic properties of transition metals in coordination environments; metalloenzymes and biomimetic compounds; and spin-related phenomena. As such, the book offers an invaluable resource for all researchers and postgraduate students interested in both fundamental and application-oriented research in the field of transition metal systems.
Author: Suyash Singh
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
Over the past century, heterogeneous catalysis has played a central role in the development of efficient chemical processes for the conversion of fossil resources to fuels and chemicals, and identification of new, sustainable routes to upgrade renewable carbon sources that minimize the ecological footprint. More recently, unprecedented advances in electronic structure theory and related computational methods have provided a major thrust to the efforts that utilize density function theory (DFT) calculations for developing fundamental atomic-level understanding of these processes, and subsequently designing new and improved catalysts. In this dissertation, a combined theoretical and experimental approach is presented to study the reaction mechanisms for the catalytic conversion of formic acid (FA) and propylene oxide on transition metals. An iterative methodology comprising of DFT calculations, reaction kinetics measurements, and mean-field microkinetic modeling is employed to determine the nature of active sites on supported catalysts, explain the experimentally observed trends, and obtain predictions for the surface environment under reaction conditions. A detailed analysis of the DFT derived thermochemistry and kinetics parameters over a wide range of transition metal surfaces is performed to identify the key reactivity descriptors for FA decomposition on transition metal catalysts, and develop semi-empirical linear correlations that are then used to develop a microkinetic modeling based framework for the identification and design of improved (active and selective) bimetallic alloy catalysts. Finally, the possible utilization and applications of these methods and ideas in other key chemical transformations are proposed, and suggestions for future work are included.
Author: Kelly E. Aldrich
Publisher:
ISBN: 9781392071069
Category : Electronic dissertations
Languages : en
Pages : 824
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Book Description
The valency or oxidation state of a transition metal in a complex plays a large role in determining the reactivity of the complex. With transition metal chemistry, historically accessible chemistry has often focused on metals in a low oxidation state. However, transformations involving transition metals in high oxidation states are of equal importance in providing complex products for use in consumer products. Expanding the applications and understanding of transition metal complexes in high oxidation states is the focus of the research presented in this dissertation. Fundamental studies of how ligands interact with high valent metals is presented in chapters 2 and 3, where a chromium(VI) model complex has been used to study bonding interactions between this d0 transition metal and phosphine ligands. Practical application of high valent titanium(IV) catalysts to C--N bond forming reactions is presented in chapters 4--6. Finally, chapters 7 and 8 focus on the changes in the character of M--N double bonds, with M=Fe and Ru, as the metal is forced to higher oxidation states. Collectively, these studies demonstrate different approaches to the same general problems and questions of how chemists can better understand and utilize high valent transitions metals to do catalytically-target desired transformations.
Author: L. Brandsma
Publisher: Springer
ISBN:
Category : Science
Languages : en
Pages : 364
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Book Description
Homogeneous catalysis is an important strategy for the synthesis of high-valued chemicals. L. Brandsma has carefully selected and checked the experimental procedures illustrating the catalytic use of copper, nickel, and palladium compounds in organic synthesis. All procedures are on a preparative scale, make economic use of solvents and catalysts, avoid toxic substances and have high yields.
Author: Christopher. Masters
Publisher: Springer
ISBN: 9781461334323
Category : Science
Languages : en
Pages : 0
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Book Description
Soluble catalysts are used extensively in many branches of chemistry and are indeed a vital constituent of many natural processes. They find wide application throughout the chemical industry where they assist in the production of several million tonnes of chemicals each year. Since homogeneous systems, especially those incorporating transition metals, often function effectively under milder conditions than their heterogeneous counterparts, they are becoming increasingly important at a time when the chemical industry in particular, and society in general, is seeking ways of conserving energy and of making the best possible use of available resources. My principal objective in· writing this book is to engender sufficient enthusiasm for, and knowledge of, the subject in the reader that he or she will be encouraged to begin, or continue, to make their own contribution to advancing our knowledge of homogeneous catalysis. After attempting to acquaint the reader with some of the ground rules I have tried to describe the .present scope, and the future potential, of this fascinating field of chemistry by drawing both on academic and on industrial data sources. This approach stems from a personal conviction that future progress could be considerably hastened by a more meaningful dialogue between chemists working both in industrial and in academic research institutions. Wherever possible, examples of the commercial application of homogeneous catalyst systems have been included and no attempt has been made in any way to disguise the many unresolved questions and exciting challenges which still pervade this rapidly developing area.
Author: Jun Deng
Publisher:
ISBN:
Category :
Languages : en
Pages : 216
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Book Description
Author: Glenn Morello
Publisher:
ISBN:
Category : Catalysis
Languages : en
Pages : 135
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Book Description
Author: Minkyu Kim (Ph. D. in chemical engineering)
Publisher:
ISBN:
Category : Catalysis
Languages : en
Pages :
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Book Description
Transition metal catalysts, including platinum, palladium, and etc., are widely used in oxygen rich applications such as catalytic combustion of natural gas in lean gas turbine, exhaust gas remediation in automobiles and power generation. Under such processes, several different oxygen phases can potentially grow on the surface. The reactivity of such oxygen phases can be dramatically different and therefore there is a need to understand both the oxygen phase that exists under reaction conditions and the reactivity of such oxygen phases. To understand reactivity and stability of important transition metal oxide surfaces including PdO(101), RuO2(110), and IrO2(110), we investigated surface chemistry including thermal reduction, CO and alkane oxidation over those surfaces by using multiscale modeling approach compared with surface science experiments. This approach is based on developing kinetic Monte Carlo (kMC) models based on DFT calculations of the elementary steps occurring on the surface. The DFT based kMC simulations allow us to elucidate the role of various mechanisms on the overall reactivity of the surfaces under low and ambient pressures, and reaction conditions.
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Transition Metal Reagents and Catalysts Innovations in Organic Synthesis Jiro Tsuji Emeritus Professor, Tokyo Institute of Technology, Japan Numerous innovative and practical synthetic methods using transition metal complexes as either catalysts or reagents have been developed over the last 35 years. Transition Metal Reagents and Catalysts combines the varied applications of transition metal complexes in a unique and timely book in this rapidly advancing area of organic synthesis. This text is an easily understandable and enjoyable read for organic chemists who are not yet familiar with organo-transition metal chemistry. Transition Metal Reagents and Catalysts presents: Complete coverage of nearly 35 years of transition metal complex chemistry An in-depth treatment of many innovative synthetic methodologies A rational classification of all reactions according to substrates and reaction mechanisms Examples of important applications of transition metal catalysed reactions. A knowledge of organic synthesis using transition metal complexes is a must for all synthetic organic chemists.; Written for chemists who wish to apply novel synthetic methods using transition metal complexes to solve problems in organic and pharmaceutical chemistry, such as synthesis of fine and bulk chemicals and natural products, Transition Metal Reagents and Catalysts is an essential reference source and an indispensible research companion.
