Readings are from the required text book:
Collman, James P., et al. Principles and Applications of Organotransition Metal Chemistry. Mill Valley, CA: University Science Books, 1987. ISBN: 9780935702514.
The table below shows the readings assigned for each lecture. The topics are taken from the chapter and section titles in the text book.
| LEC # | CH # | SEC # | TOPICS |
|---|---|---|---|
| 1 | 1 | read all sections | A Perspective. |
| 2 | read sections below | Structure and bonding | |
| 2.1 |
The relation between formal oxidation state and d electron configuration. |
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| 2.2 | ∏ Bonding in organotransition metal complexes. | ||
| 2 | 2 | read sections below | Structure and Bonding |
| 2.3 | Apparent exceptions to the 18-electron rule. | ||
| 2.4 |
Isoelectronic and isolobal analogies. |
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| 3 | read sections below |
Survey of organotransition metal complexes according to ligand. |
|
| 3.1 |
Introduction. |
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| 3.2 |
Classic lewis base donors - N, Group VIB, and Group VIIB . |
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| 3.3 |
Phosphines and other group VB donors. |
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| 3.4 |
Hydrides. Synthesis of hydrides; acidity and related properties of hydrides. |
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| 3.5 |
Carbon ligands bound principally by σ bonds. |
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| 3.6 |
Carbon ligands bound by σ and ∏ bonds. |
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| 3.7 | Organic ligands bound through more than one atom. | ||
| 3 | 3 | read sections below |
Survey of organotransition metal complexes according to ligand. |
| 3.8 |
Unsaturated nitrogen ligands. |
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| 3.9 |
Dioxygen complexes. |
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| 3.10 | Carbon dioxide. | ||
| 3.11 | Sulfur monoxide. | ||
| 3.12 | Sulfur dioxide. | ||
| 3.13 | Miscellaneous ligands. | ||
| 4 | read sections below | Ligand substitution processes. | |
| 4.1 | Introduction. | ||
| 4.2 | Definitions - Nomenclature of substitution reactions. | ||
| 4.3 |
Thermochemical considerations. |
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| 4.4 | Examples and mechanisms: Coordinatively unsaturated complexes. | ||
| 4 | 4 | read sections below |
Ligand substitution processes. |
| 4.5 |
18-Electron complexes. |
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| 4.6 |
Catalyzed and assisted ligand substitution reactions. |
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| 4.7 | Ligand substitutions in metal-metal bonded bimetallic and higher nuclearity clusters. | ||
| 5 | read sections below |
Oxidative addition and reductive elimination. |
|
| 5.1 |
Definitions, examples and scope. |
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| 5.2 |
Oxidative addition - Thermodynamic considerations. |
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| 5.3 |
Nonpolar reagents (Class A) A-B. |
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| 5.4 |
Alkane activation by C-H bond oxidative addition and related reactions. |
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| 5.5 |
Oxidative-addition of polar, electrophilic reagents, A-B. |
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| 5 | 6 | read all sections |
Intramolecular insertion reactions. |
| 7 | read all sections |
Nucleophilic attack on ligands coordinated to transition metals. |
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| 8 | read all sections |
Electrophilic attack on coordinated ligands. |
|
| 11 | read all sections |
Catalytic polymerization of olefins and acetylenes. |
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| 12 | read all sections | Catalytic reactions involving carbon monoxide. | |
| 6 | 9 | read all sections |
Metallacycles. |
| 16 | read all sections |
Synthetic applications of transition-metal carbenes and metallacycles. |
|
| 7 | 10 | read all sections |
Homogeneous catalytic hydrogenation, hydrosilation, and hydrocyanation. |
| 13 | read all sections | Synthetic applications of transition-metal hydrides. | |
| 14 | read all sections |
Synthetic applications of complexes containing metal-carbon σ bonds. |
|
| 8 | 15 | read sections below | Synthetic applications of transition-metal carbonyl compounds. |
| 15.1 | Coupling reactions. | ||
| 15.2 |
Carbonylation reactions. |
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| 9 | 15 | read sections below | Synthetic applications of transition-metal carbonyl compounds. |
| 15.3 | Decarbonylation of aldehydes and acid chlorides. | ||
| 15.4 | Reactions of metal acyl enolates with electrophiles. |
