Foto del docente

Marco Bandini

Full Professor

Department of Chemistry "Giacomo Ciamician"

Academic discipline: CHIM/06 Organic Chemistry

Research

Keywords: Asymmetric catalysis Biologically active compounds Molecular organic materials Carbocatalysis Organic synthesis

The actual scientific interests are mainly addressed to the following areas:

  1. Use of chiral organic as well as organometallic catalysts for the synthesis of enantiomerically pure compounds of pharmacological interest;
  2. Design and development of new recoverable and reusable catalysts via nanostructured deposition ono inert surfaces;
  3. Synthesis and characterization of new organometallic phosphorous for applications in opto-electronics.




Homogeneous Asymmetric Catalysis

The challenging design and realization of innovative homogeneous chiral catalysts has been addressed with the realization of efficient organometallic and metallo-free systems to be exploited in peculiar organic reactivities. Among the others the following organic reactions have been investigated: allylation of aldehydes, Michael additions, Friedel-Crafts alkylations, nitroaldol condensations, hydrosilylation of prochiral carbonyls. These studies have been object of high international recognition and diffusion.

Asymmetric Catalysis with Supported Catalysts

The recovering and reusability of chiral catalytic species is a demanding and crucial aspect in asymmetric synthesis. A new class of chiral diamino-oligothiophene ligands (DATn) have been developed and their catalytic performances assessed in nucleophilic allylic alkylations, Henry reactions and reductions of prochiral ketones. The ligands and corresponding metal complexes have been also tethered to soluble polymers (i.e. PEG5000), incarcerate into insoluble microcapsules and electrochemical deposited onto inert surfaces.  Efficiency, recoverability and reusability were demonstrated in a number of asymmetric transformations and the consequent investigations.

New Organometallic Phosphorous for OLED.

Recently, cyclometalated organometallic complexes of Ir(III) have risen to prominence in the international  scenario due to their efficiency as phosphorescent dopant for organic light emitting diodes. Within this topic, research efforts have been devoted to the synthesis, crystallographic and photophysical characterization of new classes of neutral Ir-complexes bearing unprecedented ancillary ligands. In particular, bis-oxazoline ligands have proved to suitable candidates for the production of thermally stable complexes with exceptionally high photophysical properties. Ongoing collaborations with teams of the University of Bologna and with the University of Salento (Italy) constitute an active network for this interdisciplinary research field.