Our research interests cover several aspects of the coordination chemistry of transition metal compounds.
- Functionalized bio-organometallic diiron complexes.
Diiron complexes have emerged as interesting scaffolds for the design and the development of new synthetic pathways, due to their capability of mimicking biological systems, the advantages related to the use of a nontoxic and cost-effective metal element, and the cooperativity provided by the two adjacent metal centers (two hands work better than one!). We have developed versatile and air/water stable diiron systems, and some of these complexes exhibit a promising cytotoxic activity. We are currently exploring different strategies to modify the key bridging ligand in order to modulate the behaviour of the compounds in the biological environment and to assess their catalytic potential.
- Anticancer transition metal complexes with bioactive fragments.
There are intense research efforts to develop new and efficient metal-based anticancer agents, able to overcome the limitations associated with the platinum drugs currently employed in chemotherapy. Based on the idea that the incorporation of organic fragments with documented biological functions may improve the drug efficacy, we have been involved with the synthesis and the evaluation of the anticancer activity of new transition metal complexes containing bioactive fragments, linked to the metal centre through suitable ligands.
- Sustainable organic synthesis via CO2 fixation.
Carbon dioxide is an abundant, cheap, nontoxic and therefore appealing C1 building block for synthetic chemistry. In general, we are interested in developing new environmentally friendly synthetic routes to valuable chemicals, using CO2 as a reagent under mild conditions. The feasible incorporation of CO2 into carbamates, (O2CNR2)–, allows the straightforward access to a variety of compounds of general formula [M(O2CNR2)n] (M = non transition or transition element). The catalytic behaviour of metal carbamates of non toxic metals in CO2 fixation reactions is currently under investigation.
- Activation of small molecules and stabilization of reactive organic cations by early transition metal halides.
We have contributed to the progress in the chemistry of halides of high valent metals of groups 5 and 6, with which organic compounds may undergo unusual activation pathways. Also, halo-metalato species are able to stabilize otherwise reactive organic cations (including the case of the benzene radical cation, stabilized at room temperature in a common organic solvent).
Past scientific collaborations (in alphabetical order):
Tarita Biver (University of Pisa)
Viktor Brabec (Czech Academy of Sciences, Brno)
Marco Bortoluzzi (University of Venezia)
Natalia Busto, Begoña Garcia (University of Burgos)
Sebastiano Campagna, Fausto Puntoriero (University of Messina)
Cinzia Chiappe (University of Pisa)
Federica Chiellini (University of Pisa)
Gianluca Ciancaleoni (University of Pisa)
Marcello Crucianelli (University of L’Aquila)
Ilaria Degano (University of Pisa)
Valeria Di Bussolo (University of Pisa)
Paul J. Dyson (École Polytechnique Fédérale de Lausanne)
Claudio Evangelisti (CNR, Milano)
Nicola Ferri (University of Padova)
Valentina Gandin (University of Padova)
Gilles Gasser (PSL University Paris Tech)
Tiziana Funaioli (University of Pisa)
Chiara Gabbiani, Alessandro Pratesi (University of Pisa)
Begoña Garcia Ruiz (University of Burgos)
Alceo Macchioni (University of Perugia)
Danijela Maksimovic-Ivanic, Sanja Mijatovic (University of Belgrade)
Fabio Piccinelli (University of Verona)
Francesco Pineider (University of Pisa)
Calogero Pinzino (ICCOM-CNR of Pisa)
Anna Maria Raspolli Galletti, Claudia Antonetti (University of Pisa)
Maria Lúcia Sousa Saraiva (University of Porto)
Timo Repo (University of Helsinki)
Valerio Voliani (University of Genova)
James Wilton-Ely (Imperial College, London)
Stefano Zacchini (University of Bologna)
Valerio Zanotti (University of Bologna)