
Nguồn ngoài
Inorganic Chemistry
Inorganic chemistry deals with the synthesis and behavior ofinorganic and organometallic compounds. This field covers all chemical compounds except the myriad organic compounds (carbon based compounds, usually containing C-H bonds), which are the subjects of organic chemistry.
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Mục lục· 1006 mục
- 01: Basic Concepts- Atoms
- 1.01: Introduction
- 1.02: Fundamental Particles of an Atom
- 1.03: Atomic Number Mass Number and Isotopes
- 1.3A: Nuclides Atomic Number and Mass Number
- 1.3B: Relative Atomic Mass
- 1.3C: Isotopes
- 1.04: Successes in Early Quantum Theory
- 1.4A: Some Important Successes of Classical Quantum Theory
- 1.4B: Bohr's Theory of the Atomic Spectrum of Hydrogen
- 1.05: An Introduction to Wave Mechanics
- 1.5A: Wave Mechanics of Electrons
- 1.5B: The Uncertainty Principle
- 1.5C: The Schrodinger Wave Equation
- 1.06: Atomic Orbitals
- 1.6A: Electronic Quantum Numbers
- 1.6B: The Radial Part of the Wave Function
- 1.6C: The Radial Distribution Function
- 1.6D: The Angular Part of the Wave Function
- 1.6E: Orbital Energies in a Hydrogen-like Species
- 1.6F: Size of Orbitals
- 1.6G: The Spin and Magnetic Spin Quantum Number's
- 1.6H: The ground state of Hydrogen
- 1.07: Many Electron Atoms
- 1.7A: The Helium Atom - Two Electrons
- 1.7B: Ground State Electronic Configurations - Experimental Data
- 1.7C: Penetration and Shielding
- 1.08: The Periodic Table
- 1.09: The Aufbau Principle
- 1.9A: Ground State Electronic Configurations
- 1.9B: Valence and Core Electrons
- 1.9C: Diagrammatic Representations of Electronic Configurations
- 1.10: Ionization Energies and Electron Affinities
- 02: Basic Concepts- Molecules
- 2.01: Bonding Models - An Introduction
- 2.1A: A Historical Overview
- 2.1B: Lewis Structures
- 2.02: Homonuclear Diatomic Molecules - Valence Bond Theory
- 2.2A: Uses of the term Homonuclear
- 2.2B: Covalent Bond Distance Covalent Radius and van der Waals radius
- 2.2C: Valence Bond model of Bonding in (H 2)
- 2.2D: Valence Bond model of bonding in (F 2) (O 2) and (N 2)
- 2.03: Homonuclear Diatomic Molecules - Molecular Orbital (MO) Theory
- 2.3A: An Overview of the MO Model
- 2.3b: MO theory of bonding in H
- 2.3C: MO Applied to (He 2) (Li 2) and (Be 2)
- 2.3D: MO Applied to (F 2) and (O 2)
- 2.3E: What happens if s-p separation is small
- 2.04: The Octet Rule and Isoelectronic Species
- 2.4.D: Periodic Trends
- 2.4A: The Octet Rule - First Row p-block Elements
- 2.4B: Isoelectronic Molecules
- 2.4C: The Octet Rule - Heavier p-block Elements
- 2.05: Electronegativity Values
- 2.5A: Pauling Electronegativity Values
- 2.5B: Mulliken Electronegativity Values
- 2.5C: Allred-Rochow Electronegativity Values
- 2.5D: Electronegativity - final comments
- 2.06: Dipole Moments
- 2.6A: Polar Diatomic Molecules
- 2.6B: Molecular Dipole Moments
- 2.07: MO Theory - Heteronuclear Diatomic Molecules
- 2.7A: MO Theory- Orbital Interactions
- 2.7B: Hydrogen Fluoride
- 2.7C: Carbon Monoxide
- 2.08: Molecular Shape and the VSEPR Model
- 2.8A: Valence-Shell Electron-Pair Repulsion Model
- 2.8B: Structures Derived from a Trigonal Bipyramid
- 2.8C: Limitations of the VSEPR Model
- 2.09: Molecular Shape - Stereoisomerism
- 2.9.01: Trigonal Bipyramidal Species
- 2.9.02: Trigonal Bipyramidal Structures
- 2.9A: Square Planar Species
- 2.9B: Octahedral Species
- 2.9D: High Coordination Numbers
- 2.9E: Double Bonds
- 03: Introduction to Molecular Symmetry
- 3.01: Introduction
- 3.02: Symmetry Operations and Elements
- 3.03: Successive Operations
- 3.04: Point Groups
- 3.05: Character Tables - An Introduction
- 3.06: Significance of Recognizing Symmetry Elements
- 3.07: Vibrational Spectroscopy
- 3.7A: Vibrational Spectroscopy
- 3.7C: Vibrational Spectroscopy of Linear and Bent triatomic Molecules
- 3.08: Chiral Molecules
- 04: Experimental Techniques
- 4.01: Introduction
- 4.02: Separation and Purification Techniques
- 4.2A: Gas Chromatography (GC)
- 4.2B: Liquid Chromatography (LC)
- 4.2C: High-Performance Liquid Chromatography (HPLC)
- 4.2D: Recrystallization
- 4.03: Elemental Analysis
- 4.3A: CHN Analysis by Combustion
- 4.3B: Atomic Absorption Spectroscopy (AAS)
- 4.04: Computational Analysis - Thermogravimetry (TG)
- 4.05: Mass Spectrometry
- 4.5A: Electron Ionization (EI)
- 4.5B: Fast Atom Bombardment (FAB)
- 4.5C: Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF)
- 4.5D: Electrospray Ionization (ESI)
- 4.06: Infrared and Raman Spectroscopies
- 4.6A: Energies and Wavenumbers of Molecular Vibrations
- 4.6B: The Fourier Transform Infrared (FT-IR) Spectrometer and Sample Preparation
- 4.6C: Diagnostic Absorptions
- 4.6D: Deuterium Hydrogen Exchange
- 4.6E: Raman Spectroscopy
- 4.07: Electronic Spectroscopy
- 4.7A: UV-VIS Absorption Spectroscopy
- 4.7B: Types of Absorption
- 4.7C: Absorbance and the Beer-Lambert Law
- 4.7D: Emission Spectroscopy
- 4.08: Nuclear Magnetic Resonance (NMR) Spectroscopy
- 4.8A: NMR Active Nuclei and Isotope Abundance
- 4.8B: Which Nuclei are Suitable for NMR Spectroscopic Studies
- 4.8C: Resonance Frequencies and Chemical Shifts
- 4.8D: Chemical Shift Ranges
- 4.8E: Solvents for Solution Studies
- 4.8F: Integration of Signals and Signal Broadening
- 4.8G: Homonuclear spin-spin coupling - (1H-1H)
- 4.8H: Heteronuclear spin-spin coupling - (13C-1H)
- 4.8I: Case Studies
- 4.8J: Stereochemically Non-Rigid Species
- 4.8K: Exchange Processes in Solution
- 4.09: Electron Paramagnetic Resonance (EPR) Spectroscopy
- 4.9A: What is EPR Spectroscopy
- 4.9B: The Zeeman Electronic Effect
- 4.9C: EPR Spectra
- 4.10: Mossbauer Spectroscopy
- 4.10A: The Technique of Mossbauer Spectroscopy
- 4.10B: What Can Isomer Shift Data Tell Us
- 4.11: Structure Determination - Diffraction Methods
- 4.11A: X-Ray Diffraction (XRD)
- 4.11B: Single Crystal X-Ray Diffraction
- 4.11C: Powder X-Ray Diffraction
- 4.11D: Single Crystal Neutron Diffraction
- 4.11E: Electron Diffraction
- 4.11F: Low-Energy Electron Diffraction (LEED)
- 4.11G: Structural Databases
- 4.12: Photoelectron Spectroscopy (PES UPS XPS ESCA)
- 4.13: Computational Methods
- 4.13A: Hartree-Fock Theory
- 4.13B: Density Functional Theory
- 4.13C: Huckel MO Theory
- 4.13D: Molecular Mechanisms (MM)
- 4.14: Magnetism
- 4.14.01: example magnetic moment data and their interpretation
- 4.14.02: Magnetic Moments
- 4.14.03: Magnetic Moments 1
- 4.14.04: Magnetic Susceptibility Measurements
- 4.14.05: Magnetism
- 05: Bonding in Polyatomic Molecules
- 5.01: Introduction
- 5.02: Valence Bond Theory - Hybridization of Atomic Orbitals
- 5.2A: What is Orbital Hybridization
- 5.2B: sp Hybridization
- 5.2C: sp² Hybridization
- 5.2D: sp3 Hybridization
- 5.2E: Other Hybridization Schemes
- 5.03: Valence Bond Theory - Multiple Bonding in Polyatomic Molecules
- 5.3A: Introduction
- 5.3B: (C 2H 4)
- 5.3C: (HCN)
- 5.3D: (BF 3)
- 5.04: MO Theory - The Ligand Group Orbital (LGO) Approach and Application to Triatomic Molecules
- 5.4A: MO Diagrams - Moving from Diatomic to Polyatomic Species
- 5.4B: MO Approach to Bonding in Linear (XH 2) - Symmetry Matching by Inspection
- 5.4C: MO Approach to Bonding in Linear (XH 2) - Working from Molecular Symmetry
- 5.4D: A Bent Triatomic - (H 2 O)
- 5.05: MO Theory Applied to Polyatomic Molecules (BH 3) (NH 3) and (CH 4)
- 5.5A: (BH 3)
- 5.5B: (NH 3)
- 5.5C: (CH 4)
- 5.5D: A Comparison of MO and VB Bonding Models
- 5.06: MO Theory - Bonding Analyses Soon Become Complicated
- 5.07: MO Theory - Learning to Use the Theory Objectively
- 5.7A: (pi )-Bonding in (CO 2)
- 5.7B: (NO 3-)
- 5.7C: (SF 6)
- 5.7D: Three-Center Two-Electron Interactions
- 5.7E: A More Advanced Problem - (B 2 H 6)
- 06: Structures and Energetics of Metallic and Ionic solids
- 6.01: Introduction
- 6.02: Packing of Spheres
- 6.2A: Cubic and Hexagonal Closed Packing
- 6.2B: The Unit Cell of HPC and CCP
- 1.01: The Unit Cell
- 6.2C: Interstitial Holes in HCP and CCP
- 6.2D: Non-closed Packing- Simple Cubic and Body Centered Cubic
- 6.03: The Packing of Spheres Model Applied to the Structures of Elements
- 6.3A: Group 18 Elements in the Solid State
- 6.3B: H and F Solids
- 6.3C: Solid Metallic Elements
- 6.04: Polymorphism in Metals
- 6.4A: Polymorphism - Phase Changes in the Solid State
- 6.4B: Phase Diagrams
- 6.05: Metallic Radii
- 6.06: Melting Points and Standard Enthalpies of Atomization of Metals
- 6.07: Alloys and Intermetallic Compounds
- 6.7A: Substitutional Alloys
- 6.7B: Interstitial Alloys
- 6.7C: Intermetallic Compounds
- 6.08: Bonding in Metals and Semicondoctors
- 6.8A: Electrical Conductivity and Resistivity
- 6.8B: Band Theory of Metals and Insulators
- 6.8C: The Fermi Level
- 6.8D: Band Theory of Semiconductors
- 6.09: Semiconductors
- 6.9A: Intrinsic Semiconductors
- 6.9B: Extrinsic (n-type and p-type) Semiconductors
- 6.10: Size of Ions
- 6.10A: Ionic Radii
- 6.10B: Periodic Trends in Ionic Radii
- 6.11: Ionic Lattices
- 6.11A: Structure - Rock Salt (NaCl)
- 6.11B: Structure - Caesium Chloride (CsCl)
- 6.11C: Structure - Fluorite (CaF)
- 6.11D: Structure - Antifluorite
- 6.11E: Structure - Zinc Blende (ZnS)
- 6.11F: Structure - -Cristobalite (SiO)
- 6.11H: Structure - Rutile (TiO)
- 6.11I: Structure - Layers ((CdI 2) and (CdCl 2))
- 6.11J: Structure - Perovskite ((CaTiO 3))
- 6.12: Crystal Structure of Semiconductors
- 6.13: Lattice Energy - Estimates from an Electrostatic Model
- 6.13A: Coulombic Attraction Within an Isolated Ion-Pair
- 6.13B: Coulombic Interactions in an Ionic Lattice
- 6.13C: Born Forces
- 6.13D: The Born-Lande Equation
- 6.13E: Madelung Constants
- 6.13F: Refinements to the Born-Lande Equation
- 6.13G: Overview
- 6.14: Lattice Energy - The Born-Haber Cycle
- 6.15: Lattice Energy - Calculated vs. Experimental Values
- 6.16: Application of Lattice Energies
- 6.16A: Estimation of Electron Affinities
- 6.16B: Fluoride Affinities
- 6.16C: Estimation of Standard Enthalpies of Formation and Disproportionation
- 6.16D: The Kapustinskii Equation
- 6.17: Defects in Solid State Lattices
- 6.17.E: Defects in Solid State Lattices (Exercises)
- 6.17A: Schottky Defect
- 6.17B: Frenkel Defect
- 6.17C: Experimental Observations of Schottky and Frenkel Defects
- 6.17D: Non-Stoichiometric Compounds
- 6.17E: Color Centers (F-Centers)
- 6.17F: Thermodynamic Effects of Crystal Defects
- 07: Acids bases and ions in aqueous solution
- 7.01: Introduction
- 7.1A: Acid-Base Theories and Concepts
- 7.02: Properties of Water
- 7.2A: Structure and Hydrogen Bonding
- 7.2B: The Self Ionization of Water
- 7.2C: Water as a Brnstead Acid or Base
- 7.03: Definitions and Units in Aqueous Solution
- 7.3A: Molarity and Molality
- 7.3B: Standard State
- 7.3C: Activity
- 7.04: Some Bronstead Acids and Bases
- 7.4A: Carboxylic Acids - Examples of Mono- Di- and Polybasic Acids
- 7.4B: Inorganic Acids
- 7.4C: Inorganic Bases - Hydroxides
- 7.4D: Inorganic Bases - Nitrogen Bases
- 7.05: The Energetics of Acid Dissociation in Aqueous Solution
- 7.5A: Hydrogen Halides
- 7.5B: (H 2S) (H 2Se) and (H 2Te)
- 7.06: Trends within a Series of Oxoacids (EO n(OH) m)
- 7.07: Aquated Cations - Formation and Acidic Properties
- 7.7A: Water as a Lewis Base
- 7.7B: Aquated Cations as Bronstead Acids
- 7.08: Amphoteric Oxides and Hydroxides
- 7.8A: Amphoteric Behavior
- 7.8B: Periodic Trends in Amphoteric Properties
- 7.09: Solubilities of Ionic Salts
- 7.9A: Solubility and Saturated Solutions
- 7.9B: Sparingly Soluble Salts and Solubility Products
- 7.9C: The Energetics of the Dissolution of an Ionic Salt - (Delta sol Gcirc)
- 7.9D: The Energetics of the Dissolution of an Ionic Salt - Hydration of Ions
- 7.9E: Soubilities - Some Concluding Remarks
- 7.10: Common-Ion Effect
- 7.11: Coordination Complexes - An Introduction
- 7.11A: Definitions and Terminology
- 7.11B: Investigating Coordination Complex Formation
- 7.12: Stability Constants of Coordination Complexes
- 7.12A: Determination of Stability Constants
- 7.12B: Trends in Stepwise Stability Constants
- 7.12C: Thermodynamic Considerations of Complex Formation - An Introduction
- 7.13: Factors Affecting the Stabilities of Complexes Containing Only Monodentate Ligands
- 7.13A: Ionic Size and Charge
- 7.13B: Hard and Soft Metal Centers and Ligands
- 08: Reduction and Oxidation
- 8.01: Introduction
- 8.1A: Oxidation and Reduction
- 8.1B: Oxidation States
- 8.1C: Stock Nomenclature
- 8.02: Standard Reduction Potentials E and the Relationship Between E G and K
- 8.2A: Half-Cells and Galvanic Cells
- 8.2B: Defining and Using Standard Reduction Potentials - E
- 8.2C: Dependence of Reduction Potentials on Cell Conditions
- 8.03: The Effect of Complex Formation or Precipitation on Reduction Potentials
- 8.3A: Half-Cells Involving Silver Halides
- 8.3B: Modifying the Relative Stabilities of Different Oxidation States of a Metal
- 8.04: Disproportionation Reactions
- 8.4A: Disproportionation
- 8.4B: Stabilizing Species Against Disproportionation
- 8.05: Potential Diagrams
- 8.06: Frost-Ebsworth Diagrams
- 8.6A: Frost-Ebsworth Diagrams and their Relationship to Potential Diagrams
- 8.6B: Interpretation of Frost-Ebsworth Diagrams
- 8.07: The Relationships Between Standard Reduction Potentials and Some Other Quantities
- 8.7A: Factors Influencing the Magnitudes of Standard Reduction Potentials
- 8.7B: Values of (Delta f Gcirc) for Aqueous Ions
- 8.08: Applications of Redox Reactions to the Extraction of Elements from their Ores
- 8.8A: Ellingham Diagrams
- 09: Non-aqueous Media
- 9.01: Introduction to Non-aqueous Media
- 9.02: Relative Permittivity
- 9.03: Energetics of Ionic Salt Transfer from Water to an Organic Solvent
- 9.04: Acid-Base Behaviour in Non-Aqueous Solvents
- 9.4A: Strengths of Acids and Bases
- 9.4B: Levelling and Differentiating Effects
- 9.4C: 'Acids' in Acidic Solvents
- 9.4D: Acids and Bases - A Solvent-Oriented Definition
- 9.4E: Protic and Aprotic Solvents
- 9.05: Liquid Sulfur Dioxide
- 9.06: Liquid Ammonia
- 9.6A: Physical Properties
- 9.6B: Self-Ionization of Ammonia
- 9.6C: Reactions in Liquid NH
- 9.6D: Solutions of s-block Metals in Liquid NH
- 9.6E: Redox Reactions in Liquid NH
- 9.07: Liquid Hydrogen Fluoride
- 9.7A: Physical Properties
- 9.7B: Acid-Base Behavior in Liquid HF
- 9.7C: Electrolysis in Liquid HF
- 9.08: Sulfuric Acid and Fluorosulfonic Acid
- 9.8A: Physical Properties of Sulfuric Acid
- 9.8B: Acid-Base Behaviour in Liquid (H 2 SO 4)
- 9.8C: Physical Properties of Fluorosulfonic Acid
- 9.09: Superacids
- 9.10: Bromine Trifluoride
- 9.10A: Physical Properties
- 9.10B: Fluoride Salts and Molecular Fluorides in BrF
- 9.10C: Reactions in BrF
- 9.11: Dinitrogen Tetraoxide
- 9.11A: Physical Properties of NO
- 9.11B: Reactions in NO
- 9.12: Ionic Liquids
- 9.12A: Molten Salt Solvent Systems
- 9.12B: Ionic Liquids at Ambient Temperatures
- 9.13: Supercritical Fluids
- 9.13A: Properties of Supercritical Fluids and Their Uses as Solvents
- 9.13B: Supercritical Fluids as Media for Inorganic Chemistry
- 10: Hydrogen
- 10.01: Hydrogen - The Simplest Atom
- 10.02: The (H) and (H-) Ions
- 10.2A: The Hydrogen Ion (Proton)
- 10.2B: The Hydride Ion
- 10.03: Isotopes of Hydrogen
- 10.3A: Protium and Deuterium
- 10.3B: Kinetic Isotope Effects
- 10.3C: Deuterated Compounds
- 10.3D: Tritium
- 10.04: Dihydrogen
- 10.4A: Occurence
- 10.4B: Physical Properties
- 10.4C: Synthesis and Uses
- 10.4D: Reactivity
- 10.05: Polar and Non-Polar E-H Bonds
- 10.06: Hydrogen Bonding
- 10.6A: The Hydrogen Bond
- 10.6B: Trends in Boiling Points Melting Points and Enthalpies of Vaporization for p-block Binary Hydrides
- 10.6C: Infrared Spectroscopy
- 10.6D: Solid State Structures
- 10.6E: Hydrogen Bonding in Biological Systems
- 10.07: Binary Hydrides - Classification and General Properties
- 10.7A: Classification
- 10.7B: Metallic Hydrides
- 10.7C: Saline Hydrides
- 10.7D: Molecular Hydrides and Complexes Derived from them
- 10.7E: Covalent Hydrides with Extended Structures
- 11: Group 1 - Alkali Metals
- 11.01: Introduction
- 11.02: Occurence Extraction and Uses
- 11.2A: Occurence
- 11.2B: Extraction
- 11.2C: Major Uses of the Alkali Metals and their Compounds
- 11.03: Physical Properties
- 11.3A: General Properties
- 11.3B: Atomic Spectra and Flame Tests
- 11.3C: Radioactive Isotopes
- 11.3D: NMR Active Nuclei
- 11.04: The Metals
- 11.4A: Appearance
- 11.4B: Reactivity
- 11.05: Halides
- 11.06: Oxides and Hydroxides
- 11.6A: Oxides Peroxides Superoxides Suboxides and Ozonides
- 11.6B: Hydroxides
- 11.07: Salts of Oxoacids - Carbonates and Hydrogencarbonates
- 11.08: Aqueous Solution Chemistry and Macrocyclic Complexes
- 11.8A: Hydrated Ions
- 11.8B: Complex Ions
- 11.09: Non-Aqueous Coordination Chemistry
- 12: Goup 2- Alkaline Earth Metals
- 12.01: Introduction
- 12.02: Occurence Extraction and Uses
- 12.2A: Occurrence
- 12.2B: Extraction
- 12.2C: Major Uses of Group 2 Metals and their Compounds
- 12.03: Physical Properties
- 12.3A: General Properties
- 12.3B: Flame Tests
- 12.3C: Radioactive Isotopes
- 12.04: The Metals
- 12.4A: Appearance
- 12.4B: Reactivity
- 12.05: Halides
- 12.5A: Beryllium Halides
- 12.5B: Halides of Mg Ca Sr and Ba
- 12.06: Oxides and Hydroxides
- 12.6A: Oxides and Peroxides
- 12.6B: Hydroxides
- 12.07: Salts of Oxoacids
- 12.08: Complex Ions in Aqueous Solution
- 12.8A: Aqua Species of Beryllium
- 12.8B: Aqua Species of (Mg2) (Ca2) (Sr2) and (Ba2)
- 12.8C: Complexes with Ligands other than Water
- 12.09: Complexes with Amido or Alkoxy Ligands
- 12.10: Diagonal Relationships between Li and Mg and between Be and Al
- 12.10A: Lithium and Magnesium
- 12.10B: Beryllium and Aluminium
- 13: The Group 13 Elements
- 13.01: Introduction to Group 13 Elements
- 13.02: Occurence Extraction and Uses
- 13.2A: Occurrence
- 13.2B: Extraction
- 13.2C: Major Uses of the Group 13 Elements and their Compounds
- 13.03: Physical Properties
- 13.3A: Electronic Configurations and Oxidation States
- 13.3B: NMR Active Nuclei
- 13.04: The Elements
- 13.4A: Appearance
- 13.4B: Structures of the Elements
- 13.4C: Reactivity
- 13.05: Simple Hydrides
- 13.5A: Neutral Hydrides
- 13.5B: The (MH 4-) Ions
- 13.06: Halides and Complex Halides
- 13.6A: Boron Halides - (BX 3) and (B 2X 4)
- 13.6B: Al(III) Ga(III) In(III) and Tl(III) Halides and their Complexes
- 13.6C: Lower Oxidation State Al Ga In and Tl Halides
- 13.07: Oxides Oxoacids Oxoanions and Hydroxides
- 13.7A: Boron Oxides Oxoacids and Oxoanions
- 13.7B: Aluminium Oxides Oxoacids Oxoanions and Hydroxides
- 13.7C: Oxides of Ga In and Tl
- 13.08: Compounds Containing Nitrogen
- 13.8A: Nitrides
- 13.8B: Ternary Boron Nitrides
- 13.8C: Molecular Species Containing B-N or B-P Bonds
- 13.8D: Molecular Species Containing Group 13 Metal-Nitrogen Bonds
- 13.09: Aluminium to Thallium - Salts of Oxoacids Aqueous Solution Chemistry and Complexes
- 13.9A: Aluminium Sulfate and Alums
- 13.9B: Aqua Ions
- 13.9C: Redox Reactions in Aqueous Solution
- 13.9D: Coordination Complexes of the M Ions
- 13.10: Metal Borides
- 13.11: Electron-Deficient Borane and Carbaborane Clusters - An Introduction
- 14: The Group 14 Elements
- 14.01: Introduction
- 14.02: Occurence Extraction and Uses
- 14.2A: Occurrence
- 14.2B: Extraction and Manufacture
- 14.2C: Uses
- 14.03: Physical Properties
- 14.3A: Ionization Energies and Cation Formation
- 14.3B: Some Energetic and Bonding Considerations
- 14.3C: NMR Active Nuclei
- 14.3D: Mossbauer Spectroscopy
- 14.04: Allotropes of Carbon
- 14.4A: Graphite and Diamond - Structure and Properties
- 14.4B: Graphite - Intercalation Compounds
- 14.4C: Fullerenes - Synthesis and Structure
- 14.4D: Fullerenes - Reactivity
- 14.4E: Carbon Nanotubes
- 14.05: Structural and Chemical Properties of Silicon Germanium Tin and Lead
- 14.5A: Structures
- 14.5B: Chemical Properties
- 14.06: Hydrides
- 14.6A: Binary Hydrides
- 14.6B: Halohydrides of Silicon and Germanium
- 14.07: Carbides Silicides Germides Stannides and Plumbides
- 14.7A: Carbides
- 14.7B: Silicides
- 14.7C: Zintl Ions Containing Si Ge Sn and Pb
- 14.08: Halides and Complex Halides
- 14.8A: Carbon Halides
- 14.8B: Silicon Halides
- 14.8C: Halides of Germanium Tin and Lead
- 14.09: Oxides Oxoacids and Hydroxides
- 14.9A: Oxides and Oxoacids of Carbon
- 14.9B: Silica Silicates and Aluminosilicates
- 14.9C: Oxides Hydroxides and Oxoacids of Germanium Tin and Lead
- 14.10: Siloxanes and Polysiloxanes (Silicones)
- 14.11: Sulfides
- 14.12: Cyanogen Silicon Nitride and Tin Nitride
- 14.12A: Cyanogen and its Derivatives
- 14.12B: Silicon Nitride
- 14.12C: Tin(IV) Nitride
- 14.13: Aqueous Solution Chemistry and Salts of Oxoacids of Germanium Tin and Lead
- 15: The Group 15 Elements
- 15.01: Introduction
- 15.02: Occurence Extraction and Uses
- 15.2A: Occurrence
- 15.2B: Extraction
- 15.2C: Uses
- 15.03: Physical Properties
- 15.3A: Bonding Considerations
- 15.3B: NMR Active Nuclei
- 15.3C: Radioactive Isotopes
- 15.04: The Elements
- 15.4A: Nitrogen
- 15.4B: Phosphorus
- 15.4C: Arsenic Antimony and Bismuth
- 15.05: Hydrides
- 15.5A: Trihydrides (EH 3) (E N P As Sb and Bi)
- 15.5B: Hydrides (E 2H 4) (E N P As)
- 15.5C: Chloramine and Hydroxylamine
- 15.5D: Hydrogen Azide and Azide Salts
- 15.06: Nitrides Phosphides Arsenides Antimonides and Bismuthides
- 15.6A: Nitrides
- 15.6B: Phosphides
- 15.6C: Arsenides Antimonides and Bismuthides
- 15.07: Halides Oxohalides and Complex Halides
- 15.7A: Nitrogen Halides
- 15.7B: Oxofluorides and Oxochlorides of Nitrogen
- 15.7C: Phosphorus Halides
- 15.7D: Phosphoryl Trichloride (POCl 3)
- 15.7E: Arsenic and Antimony Halides
- 15.7F: Bismuth Halides
- 15.08: Oxides of Nitrogen
- 15.8A: Dinitrogen Monoxide (N 2O)
- 15.8B: Nitrogen Monoxide (NO)
- 15.8C: Dinitrogen Trioxide (N 2O 3)
- 15.8D: Dinitrogen Tetraoxide (N 2O 4) and Nitrogen Dioxide (NO 2)
- 15.8E: Dinitrogen Pentaoxide (N 2O 5)
- 15.09: Oxoacids of Nitrogen
- 15.9A: Isomers of (H 2N 2O 2)
- 15.9B: Nitrous Acid (HNO 2)
- 15.9C: Nitric Acid (HNO 3) and its Derivatives
- 15.10: Oxides of Phosphorous Arsenic Antimony and Bismuth
- 15.10A: Oxides of Phosphorous
- 15.10B: Oxides of Arsenic Antimony and Bismuth
- 15.11: Oxoacids of Phosphorous
- 15.11A: Phosphinic Acid (H 3PO 2)
- 15.11B: Phosphonic Acid (H 3PO 3)
- 15.11C: Hypodiphosphoric Acid (H 4P 2O 6)
- 15.11D: Phosphoric Acid (H 3PO 4) and its Derivatives
- 15.11E: Chiral Phosphate Anions
- 15.12: Oxoacids of Arsenic Antimony and Bismuth
- 15.13: Phosphazenes
- 15.14: Sulfides and Selenides
- 15.14A: Sulfides and Selenides of Phosphorous
- 15.14B: Arsenic Antimony and Bismuth Sulfides
- 15.15: Aqueous Solution Chemistry and Complexes
- 16: The Group 16 Elements
- 16.01: Introduction
- 16.02: Occurrence Extraction and Uses
- 16.2A: Occurrence
- 16.2B: Extraction
- 16.2C: Uses
- 16.03: Physical Properties and Bonding Considerations
- 16.3A: NMR Active Nuclei and Isotopes as Tracers
- 16.04: The Elements
- 16.4A: Dioxygen
- 16.4B: Ozone
- 16.4C: Sulfur - Allotropes
- 16.4D: Sulfur - Reactivity
- 16.4E: Selenium and Tellurium
- 16.05: Hydrides
- 16.5A: Water (H 2O)
- 16.5B: Hydrogen Peroxide (H 2O 2)
- 16.5C: Hydrides (H 2E) (E S Se Te)
- 16.5D: Polysulfanes
- 16.06: Metal Sulfides Polysulfides Polyselenides and Polytellurides
- 16.6A: Sulfides
- 16.6B: Polysulfides
- 16.6C: Polyselenides and Polytellurides
- 16.07: Halides Oxohalides and Complex Halides
- 16.7A: Oxygen Fluorides
- 16.7B: Sulfur Fluorides and Oxofluorides
- 16.7C: Sulfur Chlorides and Oxochlorides
- 16.7D: Halides of Selenium and Tellurium
- 16.08: Oxides
- 16.8A: Oxides of Sulfur
- 16.8B: Oxides of Selenium and Tellurium
- 16.09: Oxoacids and their Salts
- 16.9A: Dithionous Acid (H 2S 2O 4)
- 16.9B: Sulfurous and Disulfurous Acids (H 2SO 3) and (H 2S 2O 5)
- 16.9C: Dithionic Acid (H 2S 2O 6)
- 16.9D: Sulfuric Acid (H 2SO 4)
- 16.9E: Fluoro- and Chlorosulfonic Acids (HSO 3F) and (HSO 3Cl)
- 16.9F: Polyoxoacids with S-O-S Units
- 16.9G: Peroxysulfuric Acids (H 2S 2O 8) and (H 2SO 5)
- 16.9H: Thiosulfuric Acid (H 2S 2O 3) and Polythionates
- 16.9I: Oxoacids of Selenium and Tellurium
- 16.10: Compounds of Sulfur and Selenium with Nitrogen
- 16.10A: Sulfur-Nitrogen Compounds
- 16.10B: Tetraselenium Tetranitride
- 16.11: Aqueous Solution Chemistry of Sulfur Selenium and Tellurium
- 17: The Group 17 Elements
- 17.01: Introduction
- 17.02: Occurrence Extraction and Uses
- 17.2A: Occurrence
- 17.2B: Extraction
- 17.2C: Uses
- 17.03: Physical Properties and Bonding Considerations
- 17.3A: NMR Active Nuclei and Isotopes as Tracers
- 17.04: The Elements
- 17.4A: Difluorine
- 17.4B: Dichlorine Dibromine and Diiodine
- 17.4C: Charge Transfer Complexes
- 17.4D: Clathrates
- 17.05: Hydrogen Halides
- 17.06: Metal Halides - Structures and Energetics
- 17.07: Interhalogen Compounds and Polyhalogen Ions
- 17.7A: Interhalogen Compounds
- 17.7B: Bonding in (XY 2-) Ions
- 17.7C: Polyhalogen Cations
- 17.7D: Polyhalide Anions
- 17.08: Oxides and Oxofluorides of Chlorine Bromine and Iodine
- 17.8A: Oxides
- 17.8B: Oxofluorides
- 17.09: Oxoacids and their Salts
- 17.9A: Hypofluorous Acid HOF
- 17.9B: Oxoacids of Chlorine Bromine and Iodine
- 17.10: Aqueous Solution Chemistry
- 18: The Group 18 Elements
- 18.01: Introduction
- 18.02: Occurrence Extraction and Uses
- 18.2A: Occurrence
- 18.2B: Extraction
- 18.2C: Uses
- 18.03: Physical Properties
- 18.3A: NMR Active Nuclei
- 18.04: Compounds of Xenon
- 18.4A: Fluorides
- 18.4B: Chlorides
- 18.4C: Oxides
- 18.4D: Oxofluorides and Oxochlorides
- 18.4E: Other Compounds of Xenon
- 18.05: Compounds of Argon Krypton and Radon
- 18.06: Group 18 Elemental Solids
- 19: d-Block Metal Chemistry - General Considerations
- 19.01: Topic Overview
- 19.02: Ground State Electronic Configurations
- 19.2A: d-block Metals Versus Transition Elements
- 19.2B: Electronic Configurations
- 19.03: Physical Properties
- 19.04: The Reactivity of the Metals
- 19.05: Characteristic Properties - A General Perspective
- 19.5A: Color
- 19.5B: Paramagnetism
- 19.5C: Complex Formation
- 19.5D: Variable Oxidation States
- 19.06: Electroneutrality Principle
- 19.07: Coordination Numbers and Geometries
- 19.7A: The Kepert Model
- 19.7B: Coordination Numbers in the Solid State
- 19.7C: Coordination Number 2
- 19.7D: Coordination Number 3
- 19.7E: Coordination Number 4
- 19.7F: Coordination Number 5
- 19.7G: Coordination Number 6
- 19.7H: Coordination Number 7
- 19.7I: Coordination Number 8
- 19.7J: Coordination Number 9
- 19.7K: Coordination Numbers of 10 and Above
- 19.08: Isomerism in d-block Metal Complexes
- 19.8A: Structural Isomerism - Ionization Isomers
- 19.8B: Structural Isomerism - Hydration Isomers
- 19.8C: Structural Isomerism - Coordination Isomerism
- 19.8D: Structural Isomerism - Linkage Isomerism
- 19.8E: Stereoisomerism - Diastereomers
- 19.8F: Stereoisomerism - Enantiomers
- 20: d-Block Metal Chemistry - Coordination Complexes
- 20.01: Introduction
- 20.1A: High- and Low-Spin States
- 20.02: Bonding in d-block Metal Complexes - Valence Bond Theory
- 20.2A: Hybridization Schemes
- 20.2B: The Limitations of VB Theory
- 20.03: Crystal Field Theory
- 20.3A: The Octahedral Crystal Field
- 20.3B: Crystal Field Stabilization Energy - High- and Low-spin Octahedral Complexes
- 20.3C: Jahn-Teller Distortions
- 20.3D: The Tetrahedral Crystal Field
- 20.3E: The Square Planar Crystal Field
- 20.3F: Other Crystal Fields
- 20.3G: Crystal Field Theory - Uses and Limitations
- 20.04: Molecular Orbital Theory - Octahedral Complexes
- 20.4A: Complexes with no Metal-Ligand (pi)-bonding
- 20.4B: Complexes with Metal-Ligand (pi)-bonding
- 20.05: Ligand Field Theory
- 20.06: Decribing Electrons in Multi-Electron Systems
- 20.6A: Quantum Number (L) and (M L) for Multi-electron Species
- 20.6B: Quantum Numbers (S) and (M S) for Multi-electron Species
- 20.6C: Microstates and Term Symbols
- 20.6D: The Quantum Numbers (J) and (M J)
- 20.6E: Ground States of Elements with Z 1-10
- 20.6F: The d Configuration
- 20.07: Electronic Spectra - Absorption
- 20.7A: Spectral Features
- 20.7B: Charge Transfer Absorptions
- 20.7C: Selection Rules
- 20.7D: Electronic Absorption Spectra of Octahedral and Tetrahedral Complexes
- 20.7E: Interpretation of Electronic Absorption Spectra - Use of Racah Parameters
- 20.7F: Interpretation of Electronic Absorption Spectra - Tanabe-Sugano Diagrams
- 20.7G: Help on using Tanabe-Sugano diagrams
- 20.08: Electronic Spectra - Emission
- 20.09: Evidence for Metal-Ligand Covalent Bonding
- 20.9A: The Nephelauxetic Effect
- 20.9B: EPR Spectroscopy
- 20.10: Magnetic Properties
- 20.10A: Magnetic Susceptibility and the Spin-only Formula
- 20.10B: Spin and Orbital Contributions to the Magnetic Moment
- 20.10C: The Effects of Temperature on Magnetic Moment
- 20.10D: Spin Crossover
- 20.10E: Ferromagnetism Antiferromagnetism and Ferrimagnetism
- 20.11: Thermodynamic Aspects - Ligand Field Stabilization Energies (LFSE)
- 20.11A: Trends in LFSE
- 20.11B: Lattice Energies and Hydration Energies of (Mn) Ions
- 20.11C: Octahedral Versus Tetrahedral Coordination - Spinels
- 20.12: Thermodynamic Aspects - The Irving-Williams Series
- 20.13: Thermodynamic Aspects - Oxidation States in Aqueous Solutions
- 21: d-Block Metal Chemistry - The First Row Metals
- 21.01: Introduction
- 21.02: Occurrence Extraction and Uses
- 21.03: Physical Properties - An Overview
- 21.04: Group 3 - Scandium
- 21.4A: Scandium Metal
- 21.4B: Scandium(III)
- 21.05: Group 4 - Titanium
- 21.5A: Titanium Metal
- 21.5B: Titanium(IV)
- 21.5C: Titanium(III)
- 21.5D: Low Oxidation States
- 21.06: Group 5 - Vanadium
- 21.6A: The Metal
- 21.6B: Vanadium(V)
- 21.6C: Vanadium(IV)
- 21.6D: Vanadium(III)
- 21.6E: Vanadium(II)
- 21.07: Group 6 - Chromium
- 21.7A: Chromium Metal
- 21.7B: Chromium(VI)
- 21.7C: Chromium(V) and Chromium(IV)
- 21.7D: Chromium(III)
- 21.7E: Chromium(II)
- 21.7F: Chromium-Chromium Multiple Bonds
- 21.08: Group 7 - Manganese
- 21.8A: The Metal
- 21.8B: Manganese(VII)
- 21.8C: Manganese(VI)
- 21.8D: Manganese(V)
- 21.8E: Manganese(IV)
- 21.8F: Manganese(III)
- 21.8G: Manganese(II)
- 21.8H: Manganese(I)
- 21.09: Group 8 - Iron
- 21.9A: The Metal
- 21.9B: Iron(VI) Iron(V) and Iron(IV)
- 21.9C: Iron(III)
- 21.9D: Iron(II)
- 21.9E: Iron in Low Oxidation States
- 21.10: Group 9 - Cobalt
- 21.10A: The Metal
- 21.10B: Cobalt(IV)
- 21.10C: Cobalt(III)
- 21.10D: Cobalt(II)
- 21.11: Group 10 - Nickel
- 21.11A: Chromium Metal
- 21.11B: Nickel(IV) and Nickel(III)
- 21.11C: Nickel(II)
- 21.11D: Nickel(I)
- 21.12: Group 11 - Copper
- 21.12A: Copper Metal
- 21.12B: Copper(IV) and Copper(III)
- 21.12C: Copper(II)
- 21.12D: Copper(I)
- 21.13: Group 12 - Zinc
- 21.13A: The Metal
- 21.13B: Zinc(II)
- 21.13C: Zinc(I)
- 22: d-Block Metal Chemistry - The Heavier Metals
- 22.01: Introduction to d-Block Metal Chemistry
- 22.02: Occurrence Extraction and Uses
- 22.03: Physical Properties
- 22.3A: Effects of the Lanthanoid Contraction
- 22.3B: Coordination Numbers
- 22.3C: NMR Active Nuclei
- 22.04: Group 3 - Yttrium
- 22.4A: The Metal
- 22.4B: Yttrium(III) Ion
- 22.05: Group 4 - Zirconium and Hafnium
- 22.5A: Group 4 - Zirconium and Hafnium
- 22.5B: Zirconium(IV) and Hafnium(IV)
- 22.5C: Lower Oxidation States of Zirconium and Hafnium
- 22.5D: Zirconium Clusters
- 22.06: Group 5 - Niobium and Tantalum
- 22.6A: Group 5 - Niobium and Tantalum
- 22.6B: Niobium(V) and Tantalum(V)
- 22.6C: Niobium(IV) and Tantalum(IV)
- 22.6D: Lower Oxidation State Halides
- 22.07: Group 6 - Molybdenum and Tungsten
- 22.7A: The Metals
- 22.7B: Molybdenum(VI) and Tungsten(VI)
- 22.7C: Molybdenum(V) and Tungsten(V)
- 22.7D: Molybdenum(IV) and Tungsten(IV)
- 22.7E: Molybdenum(III) and Tungsten(III)
- 22.7F: Molybdenum(II) and Tungsten(II)
- 22.08: Group 7 - Technetium and Rhenium
- 22.8A: The Metals
- 22.8B: High Oxidation States of Technetium and Rhenium - M(VII) M(VI) and M(V)
- 22.8C: Technetium(IV) and Rhenium(IV)
- 22.8D: Technetium(III) and Rhenium(III)
- 22.8E: Technetium(I) and Rhenium(I)
- 22.09: Group 8 - Ruthenium and Osmium
- 22.9A: The Metals
- 22.9B: High Oxidation States of Ruthenium and Osmium - M(VIII) M(VII) and M(VI)
- 22.9C: Ruthenium(V) (IV) and Osmium(V) (IV)
- 22.9D: Ruthenium(III) and Osmium(III)
- 22.9E: Ruthenium(II) and Osmium(II)
- 22.9F: Mixed-valence Ruthenium Complexes
- 22.10: Group 9 - Rhodium and Iridium
- 22.10A: The Metals
- 22.10B: High Oxidation States of Rhodium and Iridium - M(VI) and M(V)
- 22.10C: Rhodium(IV) and Iridium(IV)
- 22.10D: Rhodium(III) and Iridium(III)
- 22.10E: Rhodium(II) and Iridium(II)
- 22.10F: Rhodium(I) and Iridium(I)
- 22.11: Group 10 - Palladium and Platinum
- 22.11A: The Metals
- 22.11B: The Highest Oxidation States - M(VI) and M(V)
- 22.11C: Palladium(IV) and Platinum(IV)
- 22.11D: Palladium(III) Platinum(III) and Mixed-valence Complexes
- 22.11E: Palladium(II) and Platinum(II)
- 22.11F: Platinum(-II)
- 22.12: Group 11 - Silver and Gold
- 22.12A: The Metals
- 22.12B: Gold(V) and Silver(V)
- 22.12C: Gold(III) and Silver(III)
- 22.12D: Gold(II) and Silver(II)
- 22.12E: Gold(I) and Silver(I)
- 22.12F: Gold(-I) and Silver(-I)
- 22.13: Group 12 - Cadmium and Mercury
- 22.13A: The Metals
- 22.13B: Cadmium(II)
- 22.13C: Mercury(II)
- 22.13D: Mercury(I)
- 23: Organometallic chemistry- s-Block and p-Block Elements
- 23.01: Introduction
- 23.1A: General Methods of preparation
- 23.1B: Structure and bonding
- 23.1C: Characterization of Organometallic Complexes
- 23.02: Group 1 - Alkali Metal Organometallics
- 23.03: Group 2 Organometallics
- 23.3A: Beryllium
- 23.3B: Magnesium
- 23.3C: Calcium Strontium and Barium
- 23.04: Group 13
- 23.4A: Boron
- 23.4B: Aluminium
- 23.4C: Gallium Indium and Thallium
- 23.05: Group 14
- 23.5A: Silicon
- 23.5B: Germanium
- 23.5C: Tin
- 23.5D: Lead
- 23.5E: Coparallel and Tilted (C 5)-rings in Group 14 Metallocenes
- 23.06: Group 15
- 23.6A: Bonding Aspects and (EE) Bond Formation
- 23.6B: Arsenic Antimony and Bismuth
- 23.07: Group 16
- 23.7A: Selenium and Tellurium
- 24: Organometallic chemistry- d-block elements
- 24.01: Introduction
- 24.02: Common Types of Ligand - Bonding and Spectroscopy
- 24.2.01: Metal allyl and diene complexes
- 24.2A: (sigma)-bonded Alkyl Aryl and Related Ligands
- 24.2B: Carbonyl Ligands
- 24.2C: Hydride Ligands
- 24.2D: Phosphine and Related Ligands
- 24.2E: (pi)-bonded Organic Ligands
- 24.2F: Nitrogen Monoxide
- 24.2G: Dinitrogen
- 24.2H: Dihydrogen
- 24.03: The 18-electron Rule
- 24.04: Metal Carbonyls - Synthesis Physical Properties and Structure
- 24.4A: Synthesis and Physical Properties
- 24.4B: Structures
- 24.05: The Isolobal Principle and Application of Wade's Rules
- 24.06: Total Valence Electron Counts in d-block Organometallic Clusters
- 24.6A: Single Cage Structures
- 24.6B: Condensed Cages
- 24.6C: Limitations of Total Valence Counting Schemes
- 24.07: Types of Organometallic Reactions
- 24.7A: Substitution of CO Ligands
- 24.7B: Oxidative Addition
- 24.7C: Alkyl and Hydrogen Migrations
- 24.7D: (beta)-Hydrogen Elimination
- 24.7E: (alpha)-Hydrogen Abstraction
- 24.7F: Summary
- 24.08: Metal Carbonyls - Selected Reactions
- 24.09: Metal Carbonyl Hydrides and Halides
- 24.10: Alkyl Aryl Alkene and Alkyne Complexes
- 24.10A: (sigma)-Bonded Alkyl and Aryl Ligands
- 24.10B: Alkene Ligands
- 24.10C: Alkyne Ligands
- 24.11: Allyl and Buta-13-diene Complexes
- 24.11A: Allyl and Related Ligands
- 24.11B: Buta-13-diene and Related Ligands
- 24.12: Carbene and Carbyne Complexes
- 24.13: Complexes Containing (eta5)-cyclopentadienyl Ligands
- 24.13A: Ferrocene and other Metallocenes
- 24.13B: ((eta5-Cp) 2Fe 2(CO) 4) and Derivatives
- 24.14: Complexes Containing (eta6)- and (eta7)-ligands
- 24.14A: (eta6)-Arene Ligands
- 24.14B: Cycloheptatriene and Derived Ligands
- 24.15: Complexes Containing the (eta4)-cyclobutadiene Ligand
- 24.16: Transition Metal Complexes
- 24.16.01: Organolead Chemistry
- 24.16.02: Organomercury Chemistry
- 24.16.03: Organozinc Chemistry
- 25: Catalysis and some industrial processes
- 25.01: Introduction and Definitions
- 25.02: Catalysis - Introductory Concepts
- 25.2A: Energy Profiles for a Reaction - Catalysed Versus Non-Catalysed
- 25.2B: Catalytic Cycles
- 25.2C: Choosing a Catalyst
- 25.03: Homogeneous Catalysis - Alkene (Olefin) and Alkyne Metathesis
- 25.04: Homogeneous Catalytic Reduction of (N 2) to (NH 3)
- 25.05: Homogeneous Catalysis - Industrial Applications
- 25.5A: Alkene Hydrogenation
- 25.5B: Monsanto and Cativa Acetic Acid Synthesis
- 25.5C: Tennessee-Eastman Acetic Anhydride Process
- 25.5D: Hydroformylation (Oxo-process)
- 25.5E: Alkene Oligomerization
- 25.5F: CC cross-coupling reactions
- 25.06: Homogeneous Catalyst Development
- 25.6A: Polymer-Supported Catalysts
- 25.6B: Biphasic Catalysis
- 25.6C: d-Block Organometallic Clusters as Homogeneous Catalysts
- 25.07: Heterogeneous Catalysis - Surfaces and Interactions with Adsorbates
- 25.08: Heterogeneous Catalysis - Commercial Applications
- 25.8A: Alkene Polymerization - Ziegler-Natta Catalysis and Metallocene Catalysts
- 25.8B: Fischer-Tropsch Carbon Chain Growth
- 25.8C: Haber Process
- 25.8D: Production of (SO 3) in the Contact Process
- 25.8E: Catalytic Converters
- 25.8F: Zeolites as Catalysts for Organic Transformations - Uses of ZSM-5
- 25.09: Heterogeneous Catalysis - Organometallic Cluster Models
- 26: d-Block Metal Complexes- Reaction Mechanisms
- 26.01: Introduction
- 26.02: Ligand Substitutions - Some General Points
- 26.2A: Kinetically Inert and Labile Complexes
- 26.2B: Stoichiometric Equations Say Nothing About Mechanism
- 26.2C: Types of Substitution Mechanism
- 26.2D: Activation Parameters
- 26.03: Substitution in Square Planar Complexes
- 26.3A: Rate Equations Mechanism and the Trans-effect
- 26.3B: Ligand Nucleophilicity
- 26.04: Substitution and Racemization in Octahedral Complexes
- 26.4A: Water Exchange
- 26.4B: The Eigen-Wilkins Mechanism
- 26.4C: Stereochemistry of Substitution
- 26.4D: Base-Catalysed Hydrolysis
- 26.4E: Isomerization and Racemization of Octahedral Compleces
- 26.05: Electron-transfer Processes
- 26.5A: Inner-sphere Mechanism
- 26.5B: Outer-sphere Mechanism
- 27: f-Block Metals- Lanthanides and Actinides
- 27.01: Introduction
- 27.02: f-Orbitals and Oxidation States
- 27.03: Atoms and Ion Sizes
- 27.3A: The Lanthanoid Contraction
- 27.3B: Coordination Numbers
- 27.04: Spectroscopic and Magnetic Properties
- 27.4A: Electronic Spectra and Magnetic Moments - Lanthanoids
- 27.4B: Luminescence of Lanthanoid Complexes
- 27.4C: Electronic Spectra and Magnetic Moments - Actinoids
- 27.05: Sources of the Lanthanoids and Actinoids
- 27.5A: Occurrence and Separation of the Lanthanoids
- 27.5B: The Actinoids
- 27.06: Lanthanoid Metals
- 27.07: Inorganic Compounds and Coordination Complexes of the Lanthanoids
- 27.7A: Halides
- 27.7B: Hydroxides and Oxides
- 27.7C: Complexes of Ln(III)
- 27.08: Organometallic Complexes of the Lanthanoids
- 27.8A: (sigma)-Bonded Complexes
- 27.8B: Cyclopentadienyl Complexes
- 27.8C: Bis(arene) Derivatives
- 27.8D: Complexes Containing the (eta8)-cyclooctatetraenyl Ligand
- 27.09: The Actinoid Metals