In the future, many modern materials will be increasingly based on the assembly of preformed molecular entities. Their structural characteristics and functional prop- ties will be programmed at the molecular level and their formation as a completed entity will be achieved by self-assembly processes. This in essence is a bottom-up approach and its success will require a deep understanding not only of the chemistry of intermolecular interactions and associations but also of self-assembly processes in the condensed phase. Among various interesting innovations brought about by the development of supramolecular chemistry, supramolecular synthesis is a part- ularly powerful approach for the design and generation of molecular architectures displaying both structural and functional complexity. The combination of mol- ular synthesis (which allows chemists to design and prepare extremely sophis- cated biotic and abiotic molecules through the interconnection of atoms or group of atoms by strong covalent bonds) and supramolecular synthesis (which orch- trates the association of molecules by recognition processes through the use of weak and reversible interactions) opens up endless structural and functional possibilities. Following the perceptive observation by Dunitz that "A crystal is, in a sense, the supramolecule par excellence", molecular crystals may be seen as in?nite periodic architectures resulting from the interconnection of building blocks or tectons ca- ble of self-assembling through speci?c recognising events.

The?rsttwovolumesinthis"TemplatesinChemistry"serieshavefocused on templates that controlsolution-phase reactions. Among the templates d- cussed in these two volumes were convex and concave templates that mediate the formation of (macro)cyclic molecules and mechanically bound molecules withtheir intriguingintertwined topology.Also,three-dimensional templates that are used to imprint polymers and that organize compounds in the solid state for predestined reactions have been included in the earlier volumes. In the present volume, we extend thetemplate topologytosurfaces that act asmatricesforthecontrolledgrowthoftwo-dimensionalarrays.Naturally,the typical methods for the characterization of surfaces such as scanning probe microscopyare prominently represented in this volume. Differentlateralinteractionssuchascoordinativebondsorhydrogenbo- ing play a major role in assembling the 2D networks on surfaces in addition to the interaction of the samples with the underlying substrates. Many p- nomena that are also encountered in solution can be directly visualized on surfaces: Reversible self-assembly processes lead to the formation of large structures through multiple recognition of small building blocks and cul- nate in the engineering of crystals in two dimensions. Self-sorting processes drive the formation of highly ordered arrays through the geometric ?t of the available components. Either the surface itself is the template, for example, when clusters grow on metal oxide ?lms, or colloidal templates control the formationof macroporousnetworksonthe substrate. This volume highlightsa selection of actual complementary aspects of s- facetemplates.Webelievethatthescopeandthevarietyoftopicscoveredinthis volume will attract readers fromdifferent communities such as supramole- larchemistry,materialsciences,surfacechemistry,surfacephysicsandsurface technologyandwehopetheywillenjoythisnewvolumeonTemplatesinCh- istry.

In order to meet the ever-increasing demands for enantiopure compounds, heteroge- ous, homogeneous and enzymatic catalysis evolved independently in the past. Although all three approaches have yielded industrially viable processes, the latter two are the most widely used and can be regarded as complementary in many respects. Despite the progress in structural, computational and mechanistic studies, however, to date there is no universal recipe for the optimization of catalytic processes. Thus, a trial-and-error approach remains predominant in catalyst discovery and optimization. With the aim of complementing the well-established fields of homogeneous and enzymatic catalysis, organocatalysis and artificial metalloenzymes have enjoyed a recent revival. Artificial metalloenzymes, which are the focus of this book, result from comb- ing an active but unselective organometallic moiety with a macromolecular host. Kaiser and Whitesides suggested the possibility of creating artificial metallo- zymes as long ago as the late 1970s. However, there was a widespread belief that proteins and organometallic catalysts were incompatible with each other. This severely hampered research in this area at the interface between homogeneous and enzymatic catalysis. Since 2000, however, there has been a growing interest in the field of artificial metalloenzymes for enantioselective catalysis. The current state of the art and the potential for future development are p- sented in five well-balanced chapters. G. Roelfes, B. Feringa et al. summarize research relying on DNA as a macromolecular host for enantioselective catalysis.

V.W.-W. Yam, K.M.-C. Wong: Luminescent Molecular Rods - Transition Metal Alkynyl Complexes.- D.K. James, M. Tour: Molecular Wires.- C. Chiorboli, M.T. Indelli, F. Scandola: Photoinduced Electron/Energy Transfer Across Molecular Bridges in Binuclear Metal Complexes.- E.A. Weiss, M.R. Wasielewski, M.A. Ratner: Molecules as Wires: Molecule-Assisted Movement of Charge and Energy.- F.C. Grozema, L.D.A. Siebbeles, G.H. Gelinck, J.M. Warman: The Opto-Electronic Properties of Isolated Phenylenevinylene Molecular Wires

Despite the fact that chemical applications of ultrasound are now widely acknowledged, a detailed presentation of inorganic systems covering nano-particles, catalysis, aqueous chemistry of metallic solutions and their redox characteristics, both from a theoretical and experimental perspective has eluded researchers of this field. Theoretical and Experimental Sonochemistry Involving Inorganic Systems fills this gap and presents a concise and thorough review of this fascinating area of Sonochemistry in a single volume.

F.P. Schmidtchen: Artificial Host Molecules for the Sensing of Anions.- I. Stibor, P. Zlatuskova Chiral Recognition of Anions.- P. Lhotak: Anion Receptors Based on Calixarenes.- F. Davis, S.D. Collyer, S.P.J. Higson: The Construction and Operation of Anion Sensors - Current Status and Future Perspectives.- P.D. Beer, S.R. Bayly: Anion Sensing by Metal-Based Receptors.- C. Suksai, T. Tuntutlani: Chromogenetic Anion Sensors.- R.J.T. Houk, S.L. Tobey, E.V. Anslyn: Abiotic Guanidinium Receptors for Anion Molecular Recognition and Sensing

Molecular- and Nano-Tubes summarizes recent advancements in the synthesis, fabrication and applications of tubular structures. An interdisciplinary overview of innovative science focused on tubular structures is provided. The reader is offered an overview of the different fields that molecular and nano tubes appear in, in order to learn the fundamental basics as well as the applications of these materials. This book also: Shows how nanotechnology creates novel materials by crossing the barriers between biology and material science, electronics and optics, medicine and more Demonstrates that tubes are a fundamental element in nature and used in disparate applications such as ion channels and carbon nanotubes Molecular- and Nano-Tubes is an ideal volume for researchers and engineers working in materials science and nanotechnology.

Chemical sensors are in high demand for applications as varied as water pollution detection, medical diagnostics, and battlefield air analysis. Designing the next generation of sensors requires an interdisciplinary approach. The book provides a critical analysis of new opportunities in sensor materials research that have been opened up with the use of combinatorial and high-throughput technologies, with emphasis on experimental techniques. For a view of component selection with a more computational perspective, readers may refer to the complementary volume of Integrated Analytical Systems edited by M. Ryan et al., entitled "Computational Methods for Sensor Material Selection".

Fiberglass and Glass Technology: Energy-Friendly Compositions and Applications provides a detailed overview of fiber, float and container glass technology with special emphasis on energy- and environmentally-friendly compositions, applications and manufacturing practices which have recently become available and continue to emerge. Energy-friendly compositions are variants of incumbent fiberglass and glass compositions that are obtained by the reformulation of incumbent compositions to reduce the viscosity and thereby the energy demand. Environmentally-friendly compositions are variants of incumbent fiber, float and container glass compositions that are obtained by the reformulation of incumbent compositions to reduce environmentally harmful emissions from their melts. Energy- and environmentally-friendly compositions are expected to become a key factor in the future for the fiberglass and glass industries. This book consists of two complementary sections: continuous glass fiber technology and soda-lime-silica glass technology. Important topics covered include: o Commercial and experimental compositions and products o Design of energy- and environmentally-friendly compositions o Emerging glass melting technologies including plasma melting o Fiberglass composite design and engineering o Emerging fiberglass applications and markets Fiberglass and Glass Technology: Energy-Friendly Compositions and Applications is written for researchers and engineers seeking a modern understanding of glass technology and the development of future products that are more energy- and environmentally-friendly than current products.

It is presently well recognized that total concentrations of trace elements in any environmental compartment supply insufficient information to understand important phenomena. The distinction and separate analysis of specific chemical species are essential for understanding cycles in the aquatic environment, involving identification and quantification of sources, transport pathways, distributions and sinks, or, in the area of interactions between trace elements and organisms to understand uptake, distribution, excretion mechanisms and effects. In the past, various ways have been developed to determine the nature and extent of complexation of trace elements in natural systems. Approaches have been followed along very different lines. These have not always been fully appreciated by specialists working in even related fields of complexation research. The first International Symposium on the Complexation of Trace metals in Natural Waters was held at the Netherlands Institute for Sea Research (NIOZ, Texel, the Netherlands from 2-6 May 1983. The scientific programme was planned by the chief organizers Drs. C.J.M. Kramer and J.C. Duinker (NIOZ) together with Prof. Dr. H.W. Nurnberg (Kernforschungsanlage, Julich, Federal Republic of Germany) and Dr. M. Branica (Rudjer Boskovic Institute, Zagreb, Yugoslavia).

The contributors to this volume study macroscopic flow properties and molecular mobility in complex liquids with high internal mobility and a highly anisotropic molecular shape. Particular attention is paid to the wide variety of experimental approaches, in theory as well as in computer simulation of these difficult but very important problems. The contributions are of interest to researchers in physics as well as in engineering and chemistry.

Our understanding of the basic processes of crystal growth has meanwhile reached the level of maturity at least in the phenomenological concepts. This concerns for example the growth of pure crystals from a low-density nutrient phase like vapor or dilute solution with various aspects of pattern formation like spiral and layer growth, facetting and roughening, and the stability of smooth macroscopic shapes, as well as basic mechanisms of impurity incorporation in melt growth of (in this sense) simple materials like silicon or organic model substances. In parallel the experimental techniques to quantitatively ana lyze the various growth mechanisms have also reached a high level of reproducibility and precision, giving reliable tests on theoretical predictions. These basic concepts and appli cations to experiments have been recently reviewed by one of us (A. A. C. ) in "Modern Crystallography III. Crystal Growth" (Springer Series on Solid State Sciences, 1983). It has to be emphasized, however, that for practical applications we are still unable to quantitatively calculate many important parameters like kinetic coefficients from first principles. For mixed systems such as complex oxides, solutions and systems with chemi cal reactions, our degree of understanding is even lower. As a few examples for present achievements we note that experiments with vapour and molecular beam condensation of alkali halides confirmed the qualitatively predicted mechanisms of screw dislocations and two-dimensional nucleation for layer-growth.

Organometallic Ion Chemistry features eight chapters, written by acknowledged authorities, covering the gas-phase chemistry of organometallic ions. Topics covered include: periodic trends in gas-phase thermochemistry of transition metal-ligand systems; ab initio calculations to determine electronic structure, geometric structure, and thermochemistry of metal-containing systems; electronic state effects on metal ion reactivity; organometallic ion photochemistry; applications of gas-phase electron transfer equilibria in organometallic redox thermochemistry. Also included are state of the art mass spectrometric instrumentation used in such studies. Finally, the book features - for the first time in one place - a comprehensive list (containing over 1500 entries) of metal ion-ligand bond energies, obtained from theory and experiment. An invaluable reference source for ion chemists, organometallic chemists and surface chemists, at both expert and graduate student levels.

Dr. Alan Williams has acquired a considerable experience in work with transition metal complexes at the Universities of Cambridge and Geneva. In this book he has tried to avoid the variety of ephemeral and often contradictory rationalisations encountered in this field, and has made a careful comparison of modern opinions about chemical bond ing. In my opinion this effort is fruitful for all students and active scientists in the field of inorganic chemistry. The distant relations to group theory, atomic spectroscopy and epistemology are brought into daylight when Dr. Williams critically and pedagogic ally compares quantum chemical models such as molecular orbital theory, the more specific L. C. A. O. description and related "ligand field" theory, the valence bond treat ment (which has conserved great utility in antiferromagnetic systems with long inter nuclear distances), and discusses interesting, but not too well-defined concepts such as electronegativity (also derived from electron transfer spectra), hybridisation, and oxid ation numbers. The interdisciplinary approach of the book shows up in the careful consideration given to many experimental techniques such as vibrational (infra-red and Raman), elec tronic (visible and ultraviolet), Mossbauer, magnetic resonance, and photoelectron spectra, with data for gaseous and solid samples as well as selected facts about solution chemistry. The book could not have been written a few years ago, and is likely to re main a highly informative survey of modern inorganic chemistry and chemical physicS. Geneva, January 1979 C. K.

In this comprehensive text a systematic numerical and analytical treatment of the procedures for reducing complicated systems to a simplified reaction mechanism is presented. The results of applying the reduced reaction mechanism to a one-dimensional laminar flame are discussed. A set of premixed and non-premixed methane-air flames with simplified transport and skeletal chemistry are employed as test problems that are used later on to evaluate the results and assumptions in reduced reaction networks. The first four chapters form a short tutorial on the procedures used in formulating the test problems and in reducing reaction mechanisms by applying steady-state and partial-equilibrium approximations. The final six chapters discuss various aspects of the reduced chemistry problem for premixed and nonpremixed combustion.

This formula index contains the compounds of all three volumes. The molecular formulae show metal atoms first, followed by carbon, hydrogen, and other nonmetal atoms arranged alphabetically. The monometallic and homo- polymetallic compounds are followed by hetero-bimetallic, -trimetallic, and -polymetallic compounds. Heterometallic compounds are listed under each metal. To make the use of the index easier, for the most part, simplified linear structural formulae are given after the molecular formulae. In the case of compounds containing complicated structures, such as fused carbocyclic, hetero- cyclic, or spiro rings, index names or a combination of group symbols and the parent compound names are used. Polymeric compounds are listed under their monomer formulae. Arseno, antimono, and bismutho compounds appear under their monomeric formulae. Arsenomethane and arsenobenzene, which were isolated as a pentamer and hexamer, respectively, and also as oligomers, are listed under their monomeric formulae and under Ass and Ase, respectively. The reference fiven at the end of each entry includes the volume number under- scored, followed by the page number. An asterisk following a reference page number signifies that the name or formula of this compound in the text was corrected. The lists of corrections and additions to the three volumes are appended to this volume. Several compounds missed in the main body of this index are compiled in the "Additions" section. We wish to express our appreciation to Mrs. Mary Alice Doiron for her perse- verance shown in the preparation of this typescript.

Boron-Doped Diamond Electrodes for Electroorganic Chemistry, by Siegfried R. Waldvogel, Stamo Mentizi und Axel Kirste.- Modern Developments in Aryl Radical Chemistry, by Gerald Pratsch und Markus R. Heinrich.- Radical Additions to Chiral Hydrazones: Stereoselectivity and Functional Group Compatibility, by Gregory K. Friestad.- Hydrogen Atom Donors: Recent Developments, by Andreas Gansauer, Lei Shi, Matthias Otte, Inga Huth, Antonio Rosales, Iris Sancho-Sanz, Natalia M. Padial und J. Enrique Oltra.- Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? - A Fruitful Interplay Anyway Part 1. Radical Catalysis by Group 4 to Group 7 Elements, by Ullrich Jahn.- Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? - A Fruitful Interplay Anyway Part 2. Radical Catalysis by Group 8 and 9 Elements, by Ullrich Jahn.- Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions?: A Fruitful Interplay Anyway Part 3: Catalysis by Group 10 and 11 Elements and Bimetallic Catalysis, by Ullrich Jahn.-"