Etymology of Chemical Names gives an overview of the development of the current chemical nomenclature, tracing its sources and changing rules as chemistry progressed over the years. This book is devoted to provide a coherent picture how the trivial and systematic names shall be used and how the current IUPAC rules help to reconcile the conflicting demands.

Over the past several decades, vanadium has increasingly attracted the interest of biologists and chemists. The discovery by Henze in 1911 that certain marine ascidians accumulate the metal in their blood cells in unusually large quantities has done much to stimulate research on the role of vanadium in biology. In the intervening years, a large number of studies have been carried out to investigate the toxicity of vanadium in higher animals and to determine whether it is an essential trace element. That vanadium is a required element for a few selected organisms is now well established. Whether vanadium is essential for humans remains unclear although evidence increasingly suggests that it probably is. The discovery by Cantley in 1977 that vanadate is a potent inhibitor of ATPases lead to numerous studies of the inhibitory and stimulatory effects of vanadium on phosphate metabolizing enzymes. As a consequence vanadates are now routinely used as probes to investigate the mechanisms of such enzymes. Our understanding of vanadium in these systems has been further enhanced by the work of Tracy and Gresser which has shown striking parallels between the chemistry of vanadates and phosphates and their biological compounds. The observation by Shechter and Karlish, and Dubyak and Kleinzeller in 1980 that vanadate is an insulin mimetic agent has opened a new area of research dealing with the hormonal effects of vanadium. The first vanadium containing enzyme, a bromoperoxidase from the marine alga Ascophyllum nodosum, was isolated in 1984 by Viltner.

The intricate interactions between transition metals and ligands are at the heart of a wide variety of chemical, physical and biological phenomena. Understanding these interactions provides a challenge of the first order, cutting across many fields of modern science and impinging on numerous areas of application. The fascinating behavior of these systems has attracted the attention of experimentalists and theorists alike. In this book are collected the main lectures of the NATO ASI on "Metal-Ligand Interactions in Chemistry, Physics and Biology" held in Cetraro, Italy, in September, 1998. This event followed two previous NATO ASI held also in Cetraro in 1991 and 1994 dedicated to "Metal- Ligand Interactions: from Atoms, to Clusters, to Surfaces" and to "Metal- Ligand Interactions: Structure and Reactivity," respectively. The increasing number of participants (115) and of requests to attend (more than 400) confirms the importance and timeliness of this sequence of ASI's as well as the high level of interest for the themes treated. The lectures were organized on the basis of the following topics: -clusters and surfaces -catalysis -inorganic complexes -bioinorganic systems -new experimental techniques -theoretical methodologies and were given by well known leading experts such as: Ivano Bertini, David A. Case, Bernard Coq, Gernot Frenking, Hans J. Freund, Francesc Illas, Jacek Lipkowski, Julius Jellinek, Nino Russo, Dennis R. Vll viii Salahub, Karlheinz Schwarz, Friedrich Siebert, Benoit Simard, Edward I. Solomon and Michael Zemer.

This book introduces readers to the preparation of two-dimensional metal sulfide/oxide for CO2 photoreduction. Based on two-dimensional metal sulfide/oxide materials, this book establishes the structure-to-property relationships of photocatalyst for CO2 photoreduction, and reveals the intrinsic mechanism of the CO2 photoreduction by virtue of the in situ characterization techniques and the density functional theory calculations. It is anticipated that this book will help to identify empirical guidelines for designing and fabricating high-performance catalysts of solar-driven CO2 reduction.

Advanced fiber materials have been developed for various superior applications because of their higher mechanical flexibility, high-temperature resistance, and outstanding chemical stability. This book presents an overview of the current development of advanced fiber materials, fabrication methods, and applications. Applications covered include pollution control, environment, energy, information storage technology, optical and photonic, photocatalysis, textile, drug delivery, tumor therapy, corrosion protection applications, and a state of art of advanced fiber materials.

Preface by Sir Harold W. Kroto, FRS Although the discovery of C60 is now almost 15 years old and the extraction occurred 60 nearly ten years ago it is amazing that the range of spin-off research still seems to expand without limits. The birth of the Fullerenes has spawned fascinating research programmes in almost every area of chemistry and physics and this monograph explores a particularly interesting and important area - the behaviour of these pure carbon cages in the presence of high-energy radiation. The C molecules must also be in the space 60 between the stars (albeit in quantities too small to detect at this time) as the conditions in the atmospheres of some carbon stars appear to be almost identical to the plasmas generated in the Kratschmer-Huffman system for making C60. The conditions in space 60 are very varied as it is pervaded by a plethora of high-energy particles (photons, cosmic rays, etc.) and the chapters in this book discuss, among other things, the response of C60 and various derivatives to probing by a range of high-energy particles. Various fullerenes and fullerene salts have been examined by positron annihilation techniques, revealing details of their electronic and structural properties as well as phase transition behaviour. Muons have been implanted to enable mSR techniques to probe with high sensitivity the endohedral electronic structures of fullerenes including those in superconducting systems. Mossbauer spectroscopy can give valuable information about the interactions in certain types of organometallic complexes and in particular it can reveal the degree of charge transfer in endohedral species. Nuclear irradiation/radiochemical analytical techniques have been applied resulting in information ranging widely from the stability of the fullerene cage containing endohedral metal atoms in various oxidation states to pharmaceutical studies of the distribution of fullerenes in the internal organs of animals. Time resolved pulsed radio lysis provides information at high sensitivity enabling micromolar concentrations to be probed e.g. C60 in water in which it is almost insoluble! Redox and rate constant measurements have given useful information on photolytically generated radical ion pairs involving a variety of fullerenes. Interesting accounts of observations involving the production of rare gas endohedral species by nuclear recoil have revealed information about the recoil mechanism. From the first moment of its discovery the unique cage structure of C60 initiated thoughts about the interesting possibility of encapsulation of atoms and molecules. One possibility that immediately suggested itself was the isolation of chemically toxic radionuclides by encapsulation in the (supposedly chemically innocuous) cage for pharmaceutical purposes. The possibility of creating cages carrying a radioactive atom inside the cage and moieties outside with molecular recognition capabilities is a most exciting prospect and discussion is included of some important first steps aimed at achieving this fascinating breakthrough. Another problem dealt with in this monograph is the effect of elemental impurities which has, as our studies progress, become more and more a matter of concern and interest. Impurities can have important effects on the observed physical and chemical behaviour of fullerenes, especially when very sensitive probe techniques are applied. This valuable book reviews some detailed studies of fundamental properties of fullerenes, which are leading to a deeper understanding of their behaviour in the presence of high energy radiation. The information obtained already and that which will be garnered in future studies of the kind described here is an absolutely necessary prerequisite for success in applications.

This collection explores state-of-the-art methods and protocols for research on photodynamic therapy (PDT) and its use in a wide range of medical applications, from antiviral to anticancer. Beginning with an extensive section on in vitro and in vivo models, the volume continues with chapters on oxygen-independent photosensitizers, next-generation photosensitization strategies, contemporary insights into the immunomodulatory effects of PDT, antimicrobial effects of PDT, as well as a variety of general biochemical and molecular biological techniques. Written for the highly successful Methods in Molecular Biology series, chapters include the kind of detailed implementation advice that ensures successful results in the lab. Thorough and authoritative, Photodynamic Therapy: Methods and Protocols serves as an ideal source of inspiration for both new and established PDT scientists and a guide for designing innovative research programs in this continuously advancing and multidisciplinary field.

The second edition of this reference provides comprehensive examinations of developments in the processing and applications of carbon black, including the use of new analytical tools such as scanning tunnelling microscopy, Fourier transform infrared spectroscopy and inverse gas chromatography.;Completely rewritten and updated by numerous experts in the field to reflect the enormous growth of the field since the publication of the previous edition, Carbon Black: discusses the mechanism of carbon black formation based on recent advances such as the discovery of fullerenes; elucidates micro- and macrostructure morphology and other physical characteristics; outlines the fractal geometry of carbon black as a new approach to characterization; reviews the effect of carbon black on the electrical and thermal conductivity of filled polymers; delineates the applications of carbon black in elastomers, plastics, and zerographic toners; and surveys possible health consequences of exposure to carbon black.;With over 1200 literature citations, tables, and figures, this resource is intended for physical, polymer, surface and colloid chemists; chemical and plastics engineers; spectroscopists; materials scientists; occupational safety and health physicians; and upper-level undergraduate and graduate students in these disciplines.

Extractions of Metals from Soils and Waters represents a new emphasis in the series Modern Inorganic Chemistry, namely the impact inorganic chemistry can have on the environment. Also, this is the first volume ever to introduce the reader to all aspects of heavy metal extraction. While the primary emphasis is on complexation chemistry, attention is also paid to phase transfer aspects. Particular methods of note include electrokinetics, phytoremediation, and sensors. Aimed primarily at chemists, this book will also appeal to engineers, plant biochemists, environmental health specialists, and practitioners or students of environmental law.

The Symposium on "Transport through Membranes : Carriers. Channels and Pumps" Inaugurates the third decade of the Jerusalem Symposia. It enlarges substantially their conceptual scope by Introducing a new subject not treated there previously. In fact. It Is a topic particularly well suited for the general object of these International meetings which Is to reassemble In an exhaustive Interdisciplinary discussion chemists. physicists and biologists. theoreticians and experimentalists. The main theme of the Symposium was the presentation and evaluation of the most up-to-date data on the structural and dynamic aspects of transport through membranes within the three main pathways: through carriers. channels and pumps. This goal was fully achieved thanks to the participation of a most outstanding assembly of world's experts In the field. We wish to thank Madame Pullman. the real organizer and mainspring of this meeting. for having composed a most exciting and excellent program and for carrying It out successfully. As the twenty preceding ones this Symposium was held under the auspices of the Israel Academy of Sciences and Humanities and the Hebrew University of Jerusalem. It was sponsored by the Instltut de Blologle Physlco Chimique. Fondatlon Edmond de Rothschild of Paris. We wish to express once again our gratitude to the Baron Edmond de Rothschild for his constant and generous support which makes this continuous endeavour possible.

The current volume covers electron transfer reactions, substitution and relation reactions, and reactions of organometallic compounds.

This publication presents cleaning and etching solutions, their applications, and results on inorganic materials. It is a comprehensive collection of etching and cleaning solutions in a single source. Chemical formulas are presented in one of three standard formats - general, electrolytic or ionized gas formats - to insure inclusion of all necessary operational data as shown in references that accompany each numbered formula. The book describes other applications of specific solutions, including their use on other metals or metallic compounds. Physical properties, association of natural and man-made minerals, and materials are shown in relationship to crystal structure, special processing techniques and solid state devices and assemblies fabricated. This publication also presents a number of organic materials which are widely used in handling and general processing...waxes, plastics, and lacquers for example. It is useful to individuals involved in study, development, and processing of metals and metallic compounds. It is invaluable for readers from the college level to industrial R & D and full-scale device fabrication, testing and sales. Scientific disciplines, work areas and individuals with great interest include: chemistry, physics, metallurgy, geology, solid state, ceramic and glass, research libraries, individuals dealing with chemical processing of inorganic materials, societies and schools.

Interest in the transition metal oxides with perovskite related structures goes back to the 1950s when the sodium tungsten bronzes NaxWO3 were shown to be metallic [1 ], the system Lal_xSr~MnO3 was found to contain a ferromagnetic conductive phase [2], and La0.sSr0.sCoO3 was reported to be a ferromagnetic metal, but with a peculiar magnetization of 1.5 #a/Co atom [3]. Stoichiometric oxide perovskites have the generic formula AMO3 in which the A site is at the center of a simple cubic array of M sites; the oxide ions form (180 4)) M O M bridges to give an MO3 array of corner shared MO6/2 octahedra and the larger A cations have twelvefold oxygen coordination. Mismatch between the A O and M O equilibrium bond lengths introduces internal stresses. A compressive stress on the MO3 array is accommodated by a lowering of the M O M bond angle from 180 to (180 4)); a tensile stress on the M O M bonds is accommodated by the formation of hexagonal polytypes [4].

Molecular clusters, in the broad sense that the term is commonly understood, today comprise an enormous class of species extending into virtually every important area of chemistry: "naked" metal clusters, transition metal carbonyl clusters, hydrocarbon cages such as cubane (C H ) and dodecahedrane (C H ), 8 8 20 20 organometallic cluster complexes, enzymes containing Fe S or MoFe S 4 4 3 4 cores, high polymers based on carborane units, and, of course, the many kinds of polyhedral borane species. So large is the area spanned by these diverse classes that any attempt to deal with them comprehensively in one volume would, to say the least, be ambitious-and also premature. We are presently at a stage where intriguing relationships between the various cluster families are becoming apparent (particularly in terms of bonding descriptions), and despite large dif ferences in their chemistry an underlying unity is gradually developing in the field. For example, structural changes occurring in Fe S cores as electrons are 4 4 pumped in and out, in some measure resemble those observed in boranes and carboranes. The cleavage of alkynes via incorporation into carborane cages and subsequent cage rearrangement, a sequence familiar to boron chemists, is a thermodynamically favored process which may be related to the behavior of unsaturated hydrocarbons on metal surfaces; analogies of this sort have drawn attention from theorists and experimentalists."

The phenomenon of catalysis is found in many homogeneous and heterogeneous systems undergoing chemical change, where it effects the rates of approach to the equilibrium state in processes as diverse as those found in the stars, the earth's mantle, living organisms, and the various chemistries utilized by industry. The economies and the living standards of both developed and developing countries depend to varying degrees upon the efficacy of their chemical industries. Con sequently, this century has seen a wide exploration and expansion of catalytic chemistry together with an intensive investigation of specific, essential processes like those contributing to life-supporting agricultures. Prime among the latter must surely be the "fixation" of atmospheric nitrogen by catalytic hydrogenation to anhydrous ammonia, still the preferred synthetic precursor of the nitrogenous components of fertilizers. In each decade contemporary concepts and techniques have been used to further the understanding, as yet incomplete, of the catalyst, the adsorbates, the surface reactions, and the technology of large-scale operation. The contributors to the present volume review the state of the art, the science, and the technology; they reveal existing lacunae, and suggest ways forward. Around the turn of the century, Sabatier's school was extending the descriptive catalytic chemistry of hydrogenation by metals to include almost all types of multiple bond. The triple bond of dinitrogen, which continued to be more resistant than the somewhat similar bonds in carbon monoxide and ethyne, defied their efforts."

The six-volume CRC Handbook of Ion Exchange Resins reviews the application of ion exchange resins to inorganic analytical chemistry. Extracted from over 6,000 original publications, it presents the information in over 1,000 tables complemented by concise descriptions of analytical methods involving virtually all the elements of the periodic table. Also, the ion exchange characteristics of the elements, as well as other important information required by analysis using ion exchange resins, are presented in separate tables. The methods that allow the multi-element analysis of complex matrices are emphasized. This work includes a general discussion of the theoretical, instrumental, and other principles underlying the various applications of ion exchange resins in inorganic analytical chemistry with special attention focused on techniques based on ion chromatography.

This book focuses on chemical reactions and processing under extreme conditions-how materials react with highly concentrated active species and/or in a very confined high-temperature and high-pressure volume. Those ultimate reaction environments created by a focused laser beam, discharges, ion bombardments, or microwaves provide characteristic nano- and submicron-sized products and functional nanostructures. The book explores the chemistry and processing of metals and non-metals as well as molecules that are strongly dependent on the energy deposition processes and character of the materials. Descriptions of a wide range of topics are given from the perspective of a variety of research methodologies, material preparations, and applications. The reader is led to consider and review how a high-energy source interacts with materials, and what the key factors are that determine the quality and quantity of nanoproducts and nano-processing.

This book contains a series of papers and abstracts from the 7th Industry-University Cooperative Chemistry Program symposium held in the spring of 1989 at Texas A&M University. The symposium was larger than previous IUCCP symposia since it also celebrated the 25 years that had elapsed since the initial discovery by F. A. Cotton and his co-workers of the existence of metal-metal quadruple bonds. Cotton's discovery demonstrated that multiple bonding in inorganic systems is not governed by the same constraints observed in organic chemistry regarding s and p orbital involvement. The d orbitals are involved in the multiple bonding description. The quadruple bond involves considerable d orbital overlap between adjacent metal centers. Part I of this series of papers focuses upon the impact of this discovery and describes further contributions to the development of the field. Multiple metal-metal bonding now is known to permeate broad areas of transition metal chemistry. The understanding of metal-metal bonding that developed as a result of the discovery of multiple metal-metal bonding awakened a new chemistry involving metal clusters. Clusters were defined by Cotton to be species containing metal-metal bonding. Clusters in catalysis therefore seemed a logical grouping of papers in this symposium. Clusters play an every increasing role in the control of chemical reactions. Part II of this book describes some of the interesting new developments in this field. In Part III the papers examine the role clusters play in describing and understanding solid state materials.

This collection addresses new research and technology for increased efficiency, energy reduction, and waste minimization in mineral processing, extractive metallurgy, and recycling. Professor Patrick R. Taylor and his students have been studying these topics for the past 45 years. Chapters include new directions in:* Mineral Processing * Hydrometallurgy * Pyrometallurgy * Electrometallurgy * Metals and E waste recycling * Waste minimization (including by-product recovery) * Innovations in metallurgical engineering education and curriculum development

Assembling a program in bioinorganic chemistry that is scientifi cally relevant, well defined, and self-consistent is not an easy task. In this attempt we decided to consider zinc enzymes, copper oxidases, cytochromes and cytochrome oxidase. The choice is in part due to the great attention that the current specialized literature devotes to these topics, which are now debated among chemists, biochemists, biophysicists, etc .. We believe that hydration reactions, hydrolytic and oxidative processes have much in common from the point of view of the reaction mechanisms, the comprehension of which represents a frontier of science. For these reasons these topics have been the subject of the NATO-ASI held at San Miniato, Pisa, Italy, from May 28 to June 8, 1982. We hope we can transfer here the main conclusions of what (we believe) was a very stimulating scientific meeting. We would like to thank the local saving bank, Cassa di Risparmio di San Miniato, for helping in many ways. The financial contribution from the European Research Office of the US Army, and from the Bruker Spectrospin s.r.l., Italy, is also acknowledged. The National Science Foundation of the United States has provided a travel grant to one of the participants from the U.S.A. We are grateful to the NATO Scientific Affairs Division which provided a grant to finance this Institute."

This book presents the lectures and posters of some of the main leaders in the field of th magnesium research and medical applications delivered at the 8 International Symposium on Magnesium, which took place on 5-9 October, 1997 in Heraklion, Crete under the chairmanship of Professor Theophilos Theophanides. The meeting was sponsored by the National Technical University of Athens and Ministry of Industry, Energy and Technology. The aim of this meeting was to promote research and applications of magnesium and interface between medical doctors, clinicians and scientists in order to understand the mechanisms responsible for magnesium involvement in the pathogenesis of diseases, its biological significance, metabolism and many other utilizations which are associated with membranes and cells. The success of this interface is due to the contribution of its participants who came from all continents and to their high scientific level. The topics, which were presented, and the questions, which were asked, concerned mechanisms of mode of action of free magnesium cations, Mg2+, hydrated cations, 2 Mg2+. 6 HP, and magnesium linked cations Mg +.LxH 0, where L: ligand and x = 2 1...6 Hp. We would like to express our utmost gratitude to the sponsers and to extend our deep appreciation and thanks to all those who helped and encouraged the scientific and material organization of this meeting. We wish to thank all the members of the scientific committee and the organizing committee.

Potable water supplies that contain arsenic concentrations high enough to pose a human health hazard are a problem of international proportion. Surface water and ground water are both at risk of arsenic contamination. However, most incidences of high concentrations of arsenic have been reported for ground water, which is the subject of this book. The geochemistry of arsenic in aqueous environments is complex. This book consolidates much of what is known about the geochemistry of arsenic and provides new information on relationships between high concentrations of arsenic in ground water and geochemical environments. The subject matter of this book ranges in scope from molecular-scale geochemical processes that affect the mobility of arsenic in ground water, to arsenic contaminated ground water at the national scale. Chapters were contributed by an international group of research scientists from a broad range of backgrounds.
Information includes reviews of existing thermodynamic data for arsenic containing mineral phases and aqueous arsenic species, factors that affect adsorption of arsenic in common ground water environments, and spectroscopic techniques used to determine the chemical reactions controlling arsenic partitioning between solid and liquid phases at particle-water interfaces. A significant portion of this book is devoted to regions where high concentrations of arsenic in ground waters have a natural source. The original source of arsenic can vary; however, arsenic becomes concentrated in the solid and aqueous phases of an aquifer given appropriate geochemical conditions. Often, high arsenic concentrations in the solid phase become mobile if there is a change in ground water chemistry, either natural or anthropogenically induced. Research presented in this book covers several different geologic settings and provides explanations of the geochemical processes that have caused the arsenic concentrations observed in ground water. In situ remediation of arsenic-contaminated ground water can provide a relatively inexpensive alternative to above ground treatment. One chapter of this book discusses natural remediation of an aquifer where naturally occurring arsenic was mobilized by leachate from a landfill. Two chapters discuss results from field experiments designed to alter aquifer geochemistry in order to remove arsenic from ground water prior to withdrawal.
This book will be of interest to scientists working in the field of arsenic, health professionals interested in arsenic exposure, and water-resource managers and regulators.

The bond valence model, a description of acid-base bonding, is widely used for analysing and modelling the structures and properties of solids and liquids. Unlike other models of inorganic chemical bonding, the bond valence model is simple, intuitive, and predictive, and is accessible to anyone with a pocket calculator and a secondary school command of chemistry and physics. This new edition of 'The Chemical Bond in Inorganic Chemistry: The Bond Valence Model' shows how chemical properties arise naturally from the conflict between the constraints of chemistry and those of three-dimensional space. The book derives the rules of the bond valence model, as well as those of the traditional covalent, ionic and popular VSEPR models, by identifying the chemical bond with the electrostatic flux linking the bonded atoms. Most of the new edition is devoted to showing how to apply these ideas to real materials including crystals, liquids, glasses and surfaces. The work includes detailed examples of applications, and the final chapter explores the relationship between the flux and quantum theories of the bond.

Structural Chemistry of Inorganic Actinide Compounds is a collection of 13 reviews on structural and coordination chemistry of actinide compounds. Within the last decade, these compounds have attracted considerable attention because of their importance for radioactive waste management, catalysis, ion-exchange and absorption applications, etc. Synthetic and natural actinide compounds are also of great environmental concern as they form as a result of alteration of spent nuclear fuel and radioactive waste under Earth surface conditions, during burn-up of nuclear fuel in reactors, represent oxidation products of uranium miles and mine tailings, etc. The actinide compounds are also of considerable interest to material scientists due to the unique electronic properties of actinides that give rise to interesting physical properties controlled by the structural architecture of respective compounds.
The book provides both general overview and review of recent developments in the field, including such emergent topics as nanomaterials and nanoparticles and their relevance to the transfer of actinides under environmental conditions.
* Covers over 2,000 actinide compounds including materials, minerals and coordination polymers
* Summarizes recent achievements in the field
* Some chapters reveal (secret) advances made by the Soviet Union during the 'Cold war'