Transition Metals and Sulfur – A Strong Relationship for Life

Transition Metals and Sulfur – A Strong Relationship for Life
Author: Martha Sosa Torres
Publisher: Walter de Gruyter GmbH & Co KG
Total Pages: 610
Release: 2020-04-06
Genre: Science
ISBN: 3110588943

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Metal Ions in Life Sciences links coordination chemistry and biochemistry in their widest sense and thus increases our understanding of the relationship between the chemistry of metals and life processes; in fact, it is an old wisdom that metals are indispensable for life. The series reflects the interdisciplinary nature of Biological Inorganic Chemistry and coordinates the efforts of scientists in numerous interconnecting research fields.

Transition Metal Sulphides

Transition Metal Sulphides
Author: Th. Weber
Publisher: Springer Science & Business Media
Total Pages: 357
Release: 2013-06-29
Genre: Science
ISBN: 9401735778

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Hydrotreating catalysis with transition metal sulphides is one of the most important areas of industrial heterogeneous catalysis. The present book deals with the chemical and catalytic aspects of transition metal sulphides, focusing on their use in hydrotreating catalysis. The book¿s 12 chapters present reviews of solid-state, coordination and organometallic chemistry, surface science and spectroscopic studies, quantum chemical calculations, catalytic studies with model and real catalysts, as well as refinery processes. A presentation of state-of-the-art background to pertinent work in the field. Can be used as an introduction to the chemical and catalytic properties of transition metal sulphides as well as an advanced level reference.

Metal Complexes in Aqueous Solutions

Metal Complexes in Aqueous Solutions
Author: Arthur E. Martell
Publisher: Springer Science & Business Media
Total Pages: 259
Release: 2013-06-29
Genre: Science
ISBN: 1489914862

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Stability constants are fundamental to understanding the behavior of metal ions in aqueous solution. Such understanding is important in a wide variety of areas, such as metal ions in biology, biomedical applications, metal ions in the environment, extraction metallurgy, food chemistry, and metal ions in many industrial processes. In spite of this importance, it appears that many inorganic chemists have lost an appreciation for the importance of stability constants, and the thermodynamic aspects of complex formation, with attention focused over the last thirty years on newer areas, such as organometallic chemistry. This book is an attempt to show the richness of chemistry that can be revealed by stability constants, when measured as part of an overall strategy aimed at understanding the complexing properties of a particular ligand or metal ion. Thus, for example, there are numerous crystal structures of the Li+ ion with crown ethers. What do these indicate to us about the chemistry of Li+ with crown ethers? In fact, most of these crystal structures are in a sense misleading, in that the Li+ ion forms no complexes, or at best very weak complexes, with familiar crown ethers such as l2-crown-4, in any known solvent. Thus, without the stability constants, our understanding of the chemistry of a metal ion with any particular ligand must be regarded as incomplete. In this book we attempt to show how stability constants can reveal factors in ligand design which could not readily be deduced from any other physical technique.

Main Group and Transition Metal Complexes Supported by Carbon, Sulfur, and Selenium Donor Ligands

Main Group and Transition Metal Complexes Supported by Carbon, Sulfur, and Selenium Donor Ligands
Author: Patrick Quinlivan
Publisher:
Total Pages:
Release: 2018
Genre:
ISBN:

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For example, a mixture of [TmBut]ZnMe and Me2Cd form an equilibrium mixture with [TmBut]CdMe and Me2Zn. Furthermore, transfer of the [TmBut] ligand between the metal centers is possible too. This is demonstrated by the transfer of [TmBut] from mercury to zinc in the methyl system, [TmBut]HgMe/Me2Zn. Additionally, transfer of [TmBut] from zinc to mercury is also observed upon treatment of [TmBut]2Zn with HgI2 to afford [TmBut]HgI and [TmBut]ZnI, thereby indicating that the nature of the co-ligand has a profound effect on the thermodynamics of ligand exchange. Chapter 3 explores the coordination chemistry of the selenium donor ligand, H(sebenzimMe). H(sebenzimMe) is able to coordinate metal centers through the selenium atom in a dative fashion, and, depending upon the metal center, up to four H(sebenzimMe) ligands can coordinate the same metal. Additionally, H(sebenzimMe) can be deprotonated to form [sebenzimMe]–, allowing for the potential of an LX coordination mode, which results in bridging complexes for the metal compounds investigated.