04683nam 2200625Ia 450 991083086640332120230829003235.01-280-72357-297866107235773-527-60848-63-527-60842-7(CKB)1000000000377556(EBL)481449(OCoLC)658826749(SSID)ssj0000303473(PQKBManifestationID)11229474(PQKBTitleCode)TC0000303473(PQKBWorkID)10276234(PQKB)10084914(MiAaPQ)EBC481449(EXLCZ)99100000000037755620060726d2006 uy 0engur|n|---|||||txtccrModern terpyridine chemistry[electronic resource] /Ulrich S. Schubert, Harald Hofmeier, George R. NewkomeWeinheim Wiley-VCHc20061 online resource (239 p.)Description based upon print version of record.3-527-31475-X Includes bibliographical references and index.Modern Terpyridine Chemistry; Preface; Contents; 1 Introduction; References; 2 Syntheses of Functionalized 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.1 Introduction; 2.2 Basic Synthetic Strategies; 2.2.1 Ring Assembly; 2.2.2 Cross-Coupling Procedures; 2.3 Synthesis of 2,2 ́:6 ́,2 ́ ́-Terpyridine Derivatives; 2.3.1 4 ́-Substituted-2,2 ́:6 ́,2 ́ ́-Terpyridinoxy Derivatives; 2.3.2 4 ́-Aryl-Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.3 Other 4 ́-Functionalized 2,2 ́:6 ́ ́2 ́-Terpyridines; 2.3.4 Unsymmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.5 Symmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines2.3.6 Uniform All-Ring Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines2.3.7 Multifunctional 2,2 ́:6 ́,2 ́ ́-Terpyridines with Variable Substituents; 2.4 Summary and Outlook; References; 3 Chemistry and Properties of Terpyridine Metal Complexes; 3.1 Introduction; 3.2 Synthetic Strategies; 3.2.1 Metal Complexes; 3.2.1.1 Ruthenium Complexes; 3.2.1.2 Other Luminescent Metal Complexes; 3.3 Mononuclear Bisterpyridine Ruthenium Complexes; 3.4 Chiral Complexes; References; 4 Metallo-Supramolecular Terpyridine Architectures; 4.1 Introduction; 4.2 Dyads and Triads; 4.2.1 Switchable Dyads and Triads4.3 Supramolecular Assemblies4.3.1 Grids and Racks; 4.3.2 Helicates; 4.3.3 Rotaxanes and Catenanes; 4.3.4 Other Assemblies; 4.4 Cycles; 4.5 Fullerene Terpyridine Complexes; 4.6 Complexes Containing Biochemical Groups; References; 5 New Functional Polymers Incorporating Terpyridine Metal Complexes; 5.1 Introduction; 5.2 Polymers with Terpyridine Units in the Side Chain; 5.2.1 Polymers with Terpyridine Units in the Polymer Backbone; 5.2.2 Polymers from Rigid Organic Building Blocks; 5.2.3 Polymers from Flexible Organic Building Blocks; 5.2.4 Polymers from Polymeric Building Blocks5.2.5 Other Systems5.3 Biopolymers and Terpyridine Metal Complexes; References; 6 Functional 3-D Architectures Based on Terpyridine Complexes; 6.1 Introduction; 6.2 Dendrimers Containing Terpyridine Metal Complexes in the Dendrimer Core; 6.3 Dendrimers Containing Bisterpyridine Complexes as Non-Core Connectors; 6.4 Dendrimers Containing Bisterpyridine Complexes at the Surface; 6.5 Micelles Composed of Terpyridine-Complex-Containing Polymers; 6.6 Resins and Beads Modified with Terpyridine; References; 7 Surfaces Modified with Terpyridine Metal Complexes; 7.1 Introduction7.2 Assemblies and Layers7.3 Surface Catalysts; 7.4 Photoactive Materials; References; Subject IndexThe first book to didactically illustrate this particular, prominent class of supramolecular building-blocks covers topics ranging from terpyridine syntheses, via their chemistry and properties, supramolecular structures, and multinuclear metal complexes, right up to functionalized polymers, 3D-architectures, and surfaces.Invaluable for students and lecturers in chemistry and biochemistry, materials scientists, as well as polymer, complex and physicochemists.PyridineChemistryPyridine.Chemistry.151.79658.51Schubert U(Ulrich)864504Hofmeier Harald1680928Newkome George R(George Richard)866143MiAaPQMiAaPQMiAaPQBOOK9910830866403321Modern terpyridine chemistry4049987UNINA