Ayuda
Ir al contenido

Dialnet


Síntesis, estructura y propiedades electrónicas de nuevos sistemas push-pull basados en complejos de metales de transición

  • Autores: Gong Ming Chu Zhu
  • Directores de la Tesis: Israel Fernández López (dir. tes.), Miguel Ángel Sierra Rodríguez (dir. tes.)
  • Lectura: En la Universidad Complutense de Madrid ( España ) en 2016
  • Idioma: español
  • Tribunal Calificador de la Tesis: Roberto José Martínez Alvarez (presid.), Luis Sánchez Martín (secret.), Pedro Molina Buendía (voc.), Julia Perez-Prieto (voc.), Miquel Solà Puig (voc.)
  • Materias:
  • Enlaces
  • Resumen
    • The present work is aimed at designing novel organometallic push-pull species. To this end, different transition metal complexes, mainly based on Fischer type carbene complexes, have been synthesized and fully characterized. Their associated photophysical properties have been analysed in detail by means of experimental and computational tools. In this regard, A-Pi-D-Pi-A push-pull systems (where A = Fischer carbene complex) with enhanced Pi-conjugation have been prepared (Chapter 1). In addition, Fischer carbene complexes have been attached to the BODIPY core (Chapter 2) or to its periphery (Chapter 3) to modulate the photophysical properties of the fluorophore. Novel transition metal-BODIPY complexes having tunable emissive properties were prepared through N-directed C-H activation/cyclometallation reaction (Chapter 4). Finally, a systematic investigation of the influence of the bulkiness of the ligands on the Pd-catalyzed self-dimerization reaction of alkoxychromium(0) (Fischer) carbene complexes has been carried out (Chapter 5). Chapter 1. Chapter 1 describes the preparation of novel Pi-extended alkoxy Fischer bis(carbene) complexes A-Pi-D-Pi-A by the reaction of the corresponding dialdehydes with alkoxychromium(0) and alkoxytungsten(0) carbene complexes following the standard conditions reported by Aumann (Scheme 1)...


Fundación Dialnet

Dialnet Plus

  • Más información sobre Dialnet Plus

Opciones de compartir

Opciones de entorno