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- Wiley
More About This Title Functionalised N-Heterocyclic Carbene Complexes
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Functionalised N-Heterocyclic Carbene Complexes describes major trends in functionalised NHC ligands, aiming to assist readers in their attempts to develop and apply their own functionalised carbenes. After an introduction to the chemistry and behaviour of NHC, the book gives a detailed description of functionalised carbenes and their complexes according to a range of functional groups, each with a discussion of the synthetic route, structure, stability and performance.
Functionalised N-Heterocyclic Carbene Complexes is an essential guide to fine-tuning this important class of compounds for practitioners, researchers and advanced students working in synthetic organometallic and organic chemistry and catalysis.
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Dr Olaf Kühl, Institut für Biochemie, Ernst-Moritz-Arndt-Universität Greifswald, Germany
Olaf Kühl was recently habilitated at Greifswald University. His main research interests are in organometallic and coordination chemistry with an emphasis on ligand design, particularly in the areas of N-heterocylic germylenes, carbenes and phosphino ureas.
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Introduction.
Chapter 1 The Nature of N-Heterocyclic Carbenes.
1.1 Synthesis.
1.2 Properties of NHC.
References.
Chapter 2 Why Functionalisation?
2.1 Phosphane Mimick.
2.2 Hemilability.
2.3 Chirality.
2.4 Ligand Geometry.
2.5 Catalysis.
References.
Chapter 3 N-Heterocyclic with Neutral Tethers.
3.1 Amine Functionalities.
3.2 Oxygen-Containing Groups.
3.3 Phosphane Functionalities.
3.4 Bis-Carbene Ligands.
3.5 Tris-N-Heterocyclic Carbene Ligands.
3.6 Pincer Carbenes.
References.
Chapter 4 N-Heterocyclic with Anionic Functional Groups.
4.1 Oxygen-Containing Groups.
4.2 Nitrogen-Containing Groups.
4.3 NHC Ligands Incorporating Cp Moieties.
4.4 Transition Metal NHC Complexes Involved in the Activation of C-H Bonds.
4.5 Immobilisation of the Catalyst.
4.6 Sulfur-Containing Functional Groups.
References.
Chapter 5 Chiral N-Heterocyclic Carbenes.
References.
Chapter 6 Natural Products.
6.1 Thiazole.
6.2 Amino Acids.
6.3 Purines and Xanthines.
6.4 Carbohydrates.
6.5 Miscellaneous.
References.
Index.
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