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Intro; Preface; Contents; About the Authors; Abbreviations; 1 General Introduction; References; 2 General Characteristics of the Methods of Thermolysis of Metal Compounds; 2.1 Thermogravimetric Methods; 2.1.1 Volumetric Methods; 2.1.2 Linear Pyrolysis Method; 2.1.3 Thermolysis Induced by High-Energy Radiation; 2.1.4 Spray Pyrolysis; 2.1.5 Chemical Vapor Deposition; 2.1.6 Kinetic Approaches to the Investigation of Thermolysis of Metal Chelates; References; 3 Thermolysis of Low Molecular Weight Metal Chelates; 3.1 Metal Carboxylates; 3.1.1 Metal Formates; 3.1.2 Metal Acetates.
3.1.3 Metal Oleates3.1.4 Other Metal Monocarboxylates; 3.1.5 Metal Oxalates; 3.1.6 Metal Malonates; 3.1.7 Metal Succinates; 3.1.8 Metal Phthalates; 3.2 Metal Acetylacetonates; 3.2.1 Nickel Acetylacetonate; 3.2.2 Aluminum Acetylacetonate; 3.2.3 Copper Acetylacetonate; 3.2.4 Cobalt Acetylacetonates; 3.2.5 Zirconium Acetylacetonate; 3.2.6 Zinc Acetylacetonate; 3.2.7 Manganese Acetylacetonate; 3.2.8 Iron Acetylacetonates; 3.2.9 Cadmium Acetylacetonate; 3.2.10 Gold Acetylacetonate; 3.2.11 Platinum Acetylacetonate; 3.2.12 Palladium Acetylacetonate; 3.2.13 Ruthenium Acetylacetonates.
3.2.14 Indium Acetylacetonate3.3 Metal Chelates Based on Other O, O-Donor Ligands; 3.3.1 Metal Salicylaldehydates; 3.3.2 Metal 2-Hydroxyacetophenone; 3.3.3 Metal 2-Hydroxy-1-Naphthaldehydates; 3.3.4 Metal Glycerolates; 3.3.5 Metal Cupferronates; 3.4 Metal Chelates with N, N-Containing Ligands; 3.4.1 2,22 Diamino-5,52 Dimethyl-4,42 Bithiazole; 3.4.2 2,22 Bipyridine; 3.4.3 Ethylenediamine and Related Ligands; 3.4.4 1,10-Phenanthroline and Related Ligands; 3.4.5 Aminoiminates; 3.4.6 Pyridine Carboxamides; 3.4.7 Dimethylglyoxime; 3.5 Azomethine Metal Chelates.
3.5.1 Metal Chelates Based on 2-Hydroxyacetophenonimine3.5.2 Metal Chelates of Salicylaldimine Type; 3.5.3 Salen Chelates; 3.5.4 Salphen Chelates; 3.5.5 Metal Chelates Based on Tridentate Azomethine Ligands; 3.5.6 Metal Chelates with Other Azomethine Ligands; 3.6 Metal Chelates with N, O-Donor Ligands; 3.7 Metal Chelates with S, O-Donor Ligands; 3.7.1 Metal Chelates with N, S (Se, Te)-Donor Ligands; 3.8 Metal Dichalcogenides; 3.9 Mixed-Ligand Metal Chelates; 3.10 Polynuclear Metal Chelates; 3.11 Multicomponent Precursors Based on Metal Chelates; References.
4 Thermolysis of Polymeric Metal Chelates4.1 Synthesis of Carbon Nanomaterials; 4.2 Preparation of Metal and Metal Oxide-Carbon Nanocomposites; 4.3 Preparation of Metal Oxide Nanomaterials; 4.3.1 Transition Metal Oxides; 4.3.1.1 Zinc Oxide; 4.3.1.2 Cobalt Oxides; 4.3.1.3 Iron Oxides; 4.3.1.4 Titanium Oxides; 4.3.1.5 Manganese Oxides; 4.3.1.6 Cadmium Oxide; 4.3.1.7 Copper(II) Oxide; 4.3.1.8 Nickel Oxide; 4.3.1.9 Chromium Oxide; 4.3.1.10 Palladium Oxide; 4.3.2 Main Group Metal Oxides; 4.3.3 Rare Earth Metal Oxides; 4.3.4 Preparation of Metal Nanomaterials.
3.1.3 Metal Oleates3.1.4 Other Metal Monocarboxylates; 3.1.5 Metal Oxalates; 3.1.6 Metal Malonates; 3.1.7 Metal Succinates; 3.1.8 Metal Phthalates; 3.2 Metal Acetylacetonates; 3.2.1 Nickel Acetylacetonate; 3.2.2 Aluminum Acetylacetonate; 3.2.3 Copper Acetylacetonate; 3.2.4 Cobalt Acetylacetonates; 3.2.5 Zirconium Acetylacetonate; 3.2.6 Zinc Acetylacetonate; 3.2.7 Manganese Acetylacetonate; 3.2.8 Iron Acetylacetonates; 3.2.9 Cadmium Acetylacetonate; 3.2.10 Gold Acetylacetonate; 3.2.11 Platinum Acetylacetonate; 3.2.12 Palladium Acetylacetonate; 3.2.13 Ruthenium Acetylacetonates.
3.2.14 Indium Acetylacetonate3.3 Metal Chelates Based on Other O, O-Donor Ligands; 3.3.1 Metal Salicylaldehydates; 3.3.2 Metal 2-Hydroxyacetophenone; 3.3.3 Metal 2-Hydroxy-1-Naphthaldehydates; 3.3.4 Metal Glycerolates; 3.3.5 Metal Cupferronates; 3.4 Metal Chelates with N, N-Containing Ligands; 3.4.1 2,22 Diamino-5,52 Dimethyl-4,42 Bithiazole; 3.4.2 2,22 Bipyridine; 3.4.3 Ethylenediamine and Related Ligands; 3.4.4 1,10-Phenanthroline and Related Ligands; 3.4.5 Aminoiminates; 3.4.6 Pyridine Carboxamides; 3.4.7 Dimethylglyoxime; 3.5 Azomethine Metal Chelates.
3.5.1 Metal Chelates Based on 2-Hydroxyacetophenonimine3.5.2 Metal Chelates of Salicylaldimine Type; 3.5.3 Salen Chelates; 3.5.4 Salphen Chelates; 3.5.5 Metal Chelates Based on Tridentate Azomethine Ligands; 3.5.6 Metal Chelates with Other Azomethine Ligands; 3.6 Metal Chelates with N, O-Donor Ligands; 3.7 Metal Chelates with S, O-Donor Ligands; 3.7.1 Metal Chelates with N, S (Se, Te)-Donor Ligands; 3.8 Metal Dichalcogenides; 3.9 Mixed-Ligand Metal Chelates; 3.10 Polynuclear Metal Chelates; 3.11 Multicomponent Precursors Based on Metal Chelates; References.
4 Thermolysis of Polymeric Metal Chelates4.1 Synthesis of Carbon Nanomaterials; 4.2 Preparation of Metal and Metal Oxide-Carbon Nanocomposites; 4.3 Preparation of Metal Oxide Nanomaterials; 4.3.1 Transition Metal Oxides; 4.3.1.1 Zinc Oxide; 4.3.1.2 Cobalt Oxides; 4.3.1.3 Iron Oxides; 4.3.1.4 Titanium Oxides; 4.3.1.5 Manganese Oxides; 4.3.1.6 Cadmium Oxide; 4.3.1.7 Copper(II) Oxide; 4.3.1.8 Nickel Oxide; 4.3.1.9 Chromium Oxide; 4.3.1.10 Palladium Oxide; 4.3.2 Main Group Metal Oxides; 4.3.3 Rare Earth Metal Oxides; 4.3.4 Preparation of Metal Nanomaterials.