Supramolecular Engineering of Synthetic Metallic Materials: Conductors and Magnets: Nato Science Series C:, cartea 518
Editat de Jaume Veciana, Concepció Rovira, David Brian Amabillinoen Limba Engleză Hardback – 31 oct 1998
This book, which presents articles by foremost experts in crystal engineering, molecular conductors and magnetic magnetism, reveals the results of an interdisciplinary union that may well have a profound influence on the future of materials science. Theoretical studies reveal potential areas of interest for those investigating molecular conductors and magnets, as well as materials that exhibit both properties.
A unique survey of the state of the art appealing to all those doing research in supramolecular chemistry and materials science.
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SPRINGER NETHERLANDS – 31 oct 1998 | 1233.37 lei 6-8 săpt. |
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Specificații
ISBN-13: 9780792353119
ISBN-10: 0792353110
Pagini: 493
Ilustrații: XX, 493 p.
Dimensiuni: 155 x 235 x 29 mm
Greutate: 0.89 kg
Ediția:1999
Editura: SPRINGER NETHERLANDS
Colecția Springer
Seria Nato Science Series C:
Locul publicării:Dordrecht, Netherlands
ISBN-10: 0792353110
Pagini: 493
Ilustrații: XX, 493 p.
Dimensiuni: 155 x 235 x 29 mm
Greutate: 0.89 kg
Ediția:1999
Editura: SPRINGER NETHERLANDS
Colecția Springer
Seria Nato Science Series C:
Locul publicării:Dordrecht, Netherlands
Public țintă
ResearchCuprins
Some Current Challenges in Crystal Engineering.- Structural and Crystallographic Aspects of Supramolecular Engineering Structure-Property Relations Polymorphism and Crystal Growth.- The Computer Prediction of the Assembling of Organic Molecules into Crystals: A Perspective.- Molecular Networks: An Approach to Coordination Polymers.- The Prediction and Production of Polar Molecular Materials: From Markov’s Theory to Crystal Growth.- NMR Spectroscopy and the Development of Structural Models for Crystalline Supramolecular Solids — Applications to p-tert-butylcalix[4]arenes.- Crystal Engineering of Purely Organic Molecular Magnets: What can ab initio Computations Tell us?.- Hysteresis and Memory Effect in Supramolecular Chemistry.- Tunable Nitroxide Free Radical Ligands: From Zero-to Two-Dimensional Metal-Radical Networks.- Examples of Supramolecular Coordination Compounds and their Supramolecular Functions.- Manganoporphyrin TCNE Electron Transfer Complexes — Structure-Function Correlations.- Dithiadiazolyl Radicals as Molecular Bricks for High TcOrganic Magnets.- Host-Guest Interactions for Tuning the Magnetic Coupling in Metal Ion Clusters.- Exotic Crystal Structures and Magnetic Properties of Nitronylnitroxide Cation Radical Salts. Collapse of Spin-Gap Ground State in Distorted Antiferromagnetic Kagome Lattices.- Conductivity, Chirality and Conductivity in Layer Molecular Magnets.- Molecular Conductors and Magnets: Structure-Property Relationships.- Hybrid Materials Formed by Two Molecular Networks. Magnetic Conductors, Magnetic Multilayers and Magnetic Films.- Interplay of Conductivity and Magnetism in BETS-Derived Compounds (BETS = bis(ethylenedithio)tetraselenafulvalene).- The Flexibility of Molecular Components as a Tool in the Construction of Conducting andMagnetic Systems.- Hydrogen Bonding and Transport Properties of Molecular Conductors.- Insight into the Behavior of M(TCNQ)n(n = 1,2) Crystalline Solids and Films: X-Ray Magnetic and Conducting Properties.- Tetrathiafulvalene (TTF) Derivatives as Versatile Building Blocks: From Metals to Spin Ladders.- Novel Hyper Electron-Accepting Molecules for Development of Organic Materials.- Low-Dimensional Organic Superconductors ?-(BEDT-TTF)2Cu[N(CN)2]X, where X = Br0.5Cl0.5Br0.7Cl0.3and Br0.9I0.1.- Tetrathiafulvalenes: Building Blocks in Macrocyclic and Supramolecular Chemistry.- A New Range of Functionalised Tetrathiafulvalenes and their Cation Radical Salts: Synthetic and Solid State Studies.- New Tetrathiafulvalenes for Advanced Materials.- Metal Phosphonate Langmuir-Blodgett Films: Magnetic Monolayers and Organic/Inorganic Dual Network Assemblies.- Supramolecular Engineering of Conducting Thin Films by Covalently Hinging Electroactive Molecular Surfactants.