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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Chemical structure. ; Chemistry, Physical and theoretical. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (547 pages)
    Edition: 1st ed.
    ISBN: 9789400747715
    DDC: 541.2
    Language: English
    Note: Intro -- Foreword -- Contents -- Chapter 1 Atom -- 1.1 Ionization Potentials and Electron Affinities -- 1.1.1 Ionization Potentials of Atoms -- 1.1.2 Electron Affinity -- 1.1.3 Effective Nuclear Charge -- 1.2 Absolute Dimensions of Atoms -- 1.3 Radii of Atoms in Molecules and Crystals -- 1.3.1 Historical Outline -- 1.3.2 Metallic Radii -- 1.3.3 Covalent Radii -- 1.4 Radii of Ions in Molecules and Crystals -- 1.4.1 Methods of Estimating Ionic Radii -- 1.4.2 Experimental (bonded) Ionic Radii -- 1.4.3 Energy-Derived Ionic Radii -- 1.4.4 Ultimate Ionic Radii -- 1.4.5 Concluding Remarks -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 2 Chemical Bond -- 2.1 Historical Development of the Concept -- 2.2 Types of Bonds: Covalent, Ionic, Polar, Metallic -- 2.2.1 Ionic Bond -- 2.2.2 Covalent Bond -- 2.2.3 Polar Bond, Effective Charges of Atoms -- 2.2.4 Metallic Bond -- 2.2.5 Effective Valences of Atoms -- 2.3 Energies of the Chemical Interaction of Atoms -- 2.3.1 Bond Energies in Molecules and Radicals -- 2.3.2 Bond Energies in Crystals -- 2.3.3 Crystal Lattice Energies -- 2.3.4 Band Gaps in Solids -- 2.4 Concept of Electronegativity -- 2.4.1 Discussion About Electronegativity -- 2.4.2 Thermochemical Electronegativities -- 2.4.3 Ionization Electronegativities -- 2.4.4 Geometrical Electronegativities -- 2.4.5 Recommended System of Electronegativities of Atoms and Radicals -- 2.4.6 Equalization of Electronegativities and Atomic Charges -- 2.5 Effective Charges of Atoms and Chemical Behavior -- 2.6 Change of Chemical Bond Character under Pressure -- 2.7 Conclusions -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 3 ``Small'' Molecule -- 3.1 Introduction -- 3.2 Inorganic Molecules and Radicals -- 3.2.1 Bond Distances -- 3.2.2 Bond Angles. VSEPR Concept. , 3.2.3 Non-Stoichiometric and Unusual Molecules -- 3.3 Organic Molecules -- 3.4 Organometallic Compounds -- 3.5 Clusters -- 3.5.1 Boron Clusters -- 3.5.2 Transition Metal Clusters -- 3.5.3 Clusters of Main Group Elements -- 3.5.4 Fullerenes -- 3.6 Coordination Compounds -- Appendix -- Supplementary Table -- Supplementary References -- References -- Chapter 4 Intermolecular Forces -- 4.1 Van der Waals Interaction -- 4.2 Interdependence of the Lengths of Covalent and van der Waals Bonds -- 4.3 Van der Waals Radii -- 4.3.1 Introduction -- 4.3.2 Crystallographic van der Waals Radii -- 4.3.3 Equilibrium Radii of Atoms -- 4.3.4 Anisotropic van der Waals Radii -- 4.3.5 Concluding Remarks -- 4.4 Donor--Acceptor Interactions -- 4.5 Hydrogen Bond -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 5 Crystal Structure -- Idealised -- 5.1 Structures of Elements -- 5.1.1 Structures of Metals -- 5.1.2 Structures of Non-Metals -- 5.2 Binary Inorganic Crystalline Compounds -- 5.2.1 Crystal Structures of Halides, Oxides, Chalcogenides, Pnictides -- 5.2.2 Structures of Compounds with Diverse Bonds -- 5.3 Interconversions of Crystal Structures -- 5.4 Effective Coordination Number -- 5.5 Bond Valence (Bond Strength, Bond Order) -- 5.6 Ternary Compounds -- 5.7 Structural Features of Silicates -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 6 Crystal Structure: Real -- 6.1 Thermal Motion -- 6.2 Lindemann's Hypothesis -- 6.3 Defects in Crystals -- 6.3.1 Classification of Defects -- 6.3.2 Defects Induced by Shock Waves -- 6.3.3 Real Structure and Melting of Solids -- 6.4 Isomorphism and Solid Solutions -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 7 Amorphous State -- 7.1 Dispersing Powders -- 7.2 Amorphous Solids, Glasses -- 7.3 Structure of Melts. , 7.4 Structure of Aqueous Solutions -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 8 Between Molecule and Solid -- 8.1 Energetic Properties of Clusters and Nanoparticles -- 8.1.1 Melting Temperatures and Heats Under Transitionfrom Bulk to Nanophases -- 8.1.2 Energy Variation Under Transition from Bulk to Clusters -- 8.2 Changes of the Atomic Structure on Transition from Bulk Solids to Nanophases -- 8.3 Size Effect in the Dielectric Permittivity of Crystals -- 8.3.1 Effect of the Energy Factor -- 8.3.2 Effect of the Phase Composition on bold0mu mumu Raw of Barium Titanate -- 8.3.3 Dielectric Behavior of Ceramic Materials -- 8.3.4 Dielectric Properties of Multi-Phase Systems -- 8.4 Conclusions -- References -- Chapter 9 Phase Transition -- 9.1 Polymorphism -- 9.1.1 Polyamorphism -- 9.2 Energies of Phase Transitions -- 9.2.1 Melting Heats of Compounds -- 9.2.2 Sublimation Heats of Elements and Compounds -- 9.2.3 Evaporation Heats of Compounds -- 9.2.4 Enthalpies of Phase Transformations -- References -- Chapter 10 Extreme Conditions -- 10.1 Polymorphic Transformations Under High Static Pressures -- 10.2 Pressure-induced Amorphization and Polyamorphism -- 10.3 Effect of the Crystal Size on the Pressure of Phase Transition -- 10.4 Solid Phase Transformations Under High Dynamic Pressures -- 10.5 Detonation Transformation and Synthesis of Diamond and c-BN -- 10.6 Equations of State of Solids -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Chapter 11 Structure and Optical Properties -- 11.1 Refractive Index -- 11.1.1 Definitions, Anisotropy, Theory -- 11.1.2 Influence of Composition, Structures and Thermodynamic Conditions on Refractive Indices -- 11.2 Polarization and Dipole Moments -- 11.3 Molecular Refraction: Experiment and Calculation -- 11.3.1 Formulae of Refraction. , 11.3.2 Dependence of Refractions on the Structure and Thermodynamic Parameters -- 11.3.3 Atomic and Covalent Refractions -- 11.3.4 Ionic Refractions -- 11.3.5 Bond Refractions -- 11.4 Structural Application of Refractometry -- 11.5 Structural Applications of Spectroscopy -- 11.6 Optical Electronegativities -- Appendix -- Supplementary Tables -- Supplementary References -- References -- Index.
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  • 2
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 60 (1995), S. 4644-4646 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 870-872 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of the title complex, C10F8·C14H10, comprises mixed stacks of alternating diphenylacetylene and octafluoronaphthalene molecules, both lying at inversion centres and parallel to within 8.6 (1)°, in contrast with the herring-bone packing observed in crystals of either pure component.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of C10H10N2·C10F8, (I), comprises mixed stacks of parallel (within 2°) neutral molecules, overlapping in a `graphitic' mode. Molecular geometry and UV–visible spectra indicate the absence of charge transfer. Structure (I) in space group P21 is close to P21/c and pseudo-isostructural with the 1:1 complex of naphthalene and C10F8, hence the crystal packing of (I) is governed largely by quadrupole–quadrupole interactions, hydrogen bonding of NH2 groups (including a relatively strong N—H...F bond of 2.16 Å) being less important.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m235-m236 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title complex, [PdI2(dppe)], where dppe is 1,2-bis(diphenylphosphino)ethane (C26H24P2), has a square-planar coordination of the Pd atom with a small tetrahedral distortion and an envelope conformation of the five-membered metallocycle, similar to those observed in [PdI2(dppe)]·CHCl3.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m301-m304 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In the title compound, [PdCl2(C26H24P2)]·3CDCl3, the [PdCl2(dppe)] molecule adopts a distorted square-planar metal coordination and an asymmetrical twist conformation of the five-membered metallocycle. The structure contains infinite channels filled with deuterochloroform of crystallization and displays an (a, b/2, c) subcell.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m308-m309 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Re-investigation of [NiCl2(PPh3)2]·2CH2Cl2 at 120 K yielded much more accurate geometric parameters than the earlier room temperature study and confirmed the main conclusion of the latter: the Ni—P and Ni—Cl bonds in this centrosymmetric square-planar complex [2.2439 (5) and 2.1672 (5) Å] are significantly shorter than in the tetrahedral solvent-free [NiCl2(PPh3)2].
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m524-m526 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, [Cu2Cl4(C20H18N2O)2], is a centrosymmetric dimer bridged through the Cl atoms. The bridging Cu2Cl2 unit is planar and each CuII ion has two different distances to the bridging Cl atom. The CuII ions are coordinated to three Cl and two N atoms in a square-pyramidal disposition. Hydrogen bonds are formed by –OH and –NH with the Cl atoms.
    Type of Medium: Electronic Resource
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