Buch, Englisch, 153 Seiten, Format (B × H): 160 mm x 241 mm, Gewicht: 455 g
Reihe: Springer Theses
Buch, Englisch, 153 Seiten, Format (B × H): 160 mm x 241 mm, Gewicht: 455 g
Reihe: Springer Theses
ISBN: 978-981-99-4120-9
Verlag: Springer Nature Singapore
Transition-metal-catalyzed C(sp2)–H/C(sp2)–H coupling has attracted much attention as one of the most straightforward methods to construct C(sp2)–C(sp2) bonds. However, application of this ideal transformation to the synthesis of redox-sensitive pi-materials was hindered by the requirement of a strong oxidant for catalyst turnover. This limitation originates primarily from the large redox potential of conventional transition-metal catalysts such as palladium and rhodium.
This thesis shows that the efficiency of C–H activation was significantly improved by introduction of a new conjugated tridentate phosphine ligand, giving direct access to polymeric thiophene materials from simple thiophene monomers. Considering the importance of environmentally friendly organic synthesis in terms of UN Sustainable Development Goals, the reactions described herein highlight the potential of iron, the most abundant transition-metal on earth, for the direct synthesis of functional small molecules and polymers of importance in energy device applications.
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Weitere Infos & Material
1. General Introduction.- 2. Iron-Catalyzed Regioselective Thienyl C–H/C–H Homocoupling.- 3. Development of a Synthetic Method for Tridentate Phosphine Ligands.- 4. Iron-Catalyzed Regioselective Thienyl C–H/C–H Polycondensation.- 5. Iron-Catalyzed Oxidative C–H Alkenylation of Thiophenes with Enamines.- 6. Conclusions and Perspectives.