Metallofoldamers : supramolecular architectures from helicates to biomimetics /
Metallofoldamers are oligomers that fold into three-dimensional structures in a controlled manner upon coordination with metal ions. Molecules in this class have shown an impressive ability to form single-handed helical structures and other three-dimensional architectures. Several metallofoldamers h...
Clasificación: | Libro Electrónico |
---|---|
Otros Autores: | , |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Chichester, West Sussex, United Kingdom :
Wiley,
2013.
|
Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Metallofoldamers: Supramolecular Architectures from Helicates to Biomimetics; Contents; List of Contributors; Foreword; Preface; 1 Metalloproteins and Metallopeptides
- Natural Metallofoldamers; 1.1 Introduction; 1.2 Metalloproteins; 1.2.1 Metalloproteins are Nature's "Metallofoldamers!"; 1.2.2 Metal-Triggered Conformational Change of Proteins; 1.2.3 Conformational Change of Metalloproteins Caused by Ligand Binding; 1.2.4 Protein Misfolding: Causes and Implications
- Cu, Zn-Superoxide Dismutase; 1.3 Metallopeptides; 1.3.1 Antibiotic Metallopeptides.
- 2.5 Applications2.6 Conclusions and Outlook; References; 3 Self-Assembly Principles of Helicates; 3.1 Introduction; 3.2 Thermodynamic Considerations in Self-Assembly; 3.2.1 Mononuclear Coordination Complexes; 3.2.2 Extension to Polynuclear Edifices; 3.3 Cooperativity in Self-Assembly; 3.3.1 Allosteric Cooperativity; 3.3.2 Chelate Cooperativity; 3.3.3 Interannular Cooperativity; 3.4 Kinetic Aspects of Multicomponent Organization; 3.5 Understanding Self-Assembly Processes; 3.5.1 Assessment of Cooperativity; 3.5.2 Thermodynamic Modelling; 3.5.3 Solvation Energies and Electrostatic Interactions.
- 3.6 Secondary Structure and Stabilizing Interactions3.7 Conclusions; References; 4 Structural Aspects of Helicates; 4.1 Introduction; 4.2 Structural Dynamics; 4.3 Template Effects; 4.4 Sequence Selectivity; 4.5 Self-Sorting Effects in Helicate Formation; 4.6 Diastereoselectivity I
- "Meso"-Helicate versus Helicate Formation; 4.7 Diastereoselectivity II
- Enantiomerically Pure Helicates from Chiral Ligands; 4.7.1 2,2'-Bipyridine Ligands; 4.7.2 2,2':6',2''-Terpyridine and 2,2':6',2'':6'',2-Quaterpyridine Ligands; 4.7.3 2-Pyridylimine Ligands; 4.7.4 Further Hexadentate N-Donor Ligands.