FABIO MARCHETTI

Full Professor (Professore Ordinario)

University of Pisa

Italy

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Fabio Marchetti is a Full Professor at the Università di Pisa in Italy. His research focuses on organometallic chemistry, particularly the development of anticancer agents and electrocatalysts, as evidenced by his recent publications on diiron complex structures and their biological activities. With a keen interest in catalytic processes, he has explored the hydrogenation of carbon dioxide and the biological evaluation of novel ligands.

FABIO MARCHETTI

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Articles (28)

Biological evaluation of a novel Schiff base ligand as an antioxidant agent: Synthesis, characterization and DFT computations of its Ni(II) and Cu(II) complexes

Invasiveness modulation of glioma cells by copper complex-loaded nanoarchitectures

Carbon dioxide hydrogenation to formate catalyzed by highly active Ru-tris(pyrazolyl)methane complexes

Incorporating alkylthio groups provides potent in vitro anticancer activity to water-soluble and aqueous-stable diiron(I) bis-cyclopentadienyl complexes

Anticancer Iron–Iridium Organometallic Conjugates

Oxidative Chlorination Reactions of [Nb(CO)6]− in the Presence of N‐ and P‐Donors

Anticancer activity promoted by ligand diversity in diiron thiocarbyne complexes

The effect of a varying pyridine ligand on the anticancer activity of Diiron(I) bis-cyclopentadienyl complexes

2D and 3D anticancer activity of diiron bis-cyclopentadienyl complexes incorporating flurbiprofen and chlorambucil

Effective electrocatalysts for hydrogen production from acetic acid by screening of monodentate ligands in cationic diiron hetero-carbyne complexes

Multisite Amino‐Allylidene Ligands from Thermal CO Elimination in Diiron Complexes and Catalytic Activity in Hydroboration Reactions

1,3,5-Triaza-7-phosphaadamantane and Cyclohexyl Groups Impart to Di-Iron(I) Complex Aqueous Solubility and Stability, and Prominent Anticancer Activity in Cellular and Animal Models

Aminocarbyne-Alkyne Coupling in Diruthenium Complexes: Exploring the Anticancer Potential of the Resulting Vinyliminium Complexes and Comparison with Diiron Homologues

Cyanide Addition to Diiron and Diruthenium Bis-Cyclopentadienyl Complexes with Bridging Hydrocarbyl Ligands

FETPY: a Diiron(I) Thio–Carbyne Complex with Prominent Anticancer Activity In Vitro and In Vivo

The serendipitous isolation of a dinuclear iron(II) complex with a bridging η2: η2-trans-butadiene reveals the stabilizing effect of benzyl-isocyanide co-ligands

Mixed valence triiron complexes from the conjugation of [FeIFeI] and [FeII] complexes via intermolecular carbyne/alkyne coupling

Synthesis and studies of aqueous-stable diruthenium aminocarbyne complexes uncovered an N-indolyl derivative as a prospective anticancer agent

Piano Stool Iron Complexes with Isocyanide Ligands

Diiron Aminocarbyne Complexes with NCE− Ligands (E = O, S, Se)

Diiron bis‐cyclopentadienyl complexes as transfer hydrogenation catalysts: The key role of the bridging aminocarbyne ligand

Adding Diversity to Diiron Aminocarbyne Complexes with Amine Ligands

Anticancer Potential of Diruthenium Complexes with Bridging Hydrocarbyl Ligands from Bioactive Alkynols

Adding Diversity to a Diruthenium Biscyclopentadienyl Scaffold via Alkyne Incorporation: Synthesis and Biological Studies

Triazine Chalcogenones from Thiocyanate or Selenocyanate Addition to Tetrazine Ligands in Ruthenium Arene Complexes

Construction of Two-Faced (Hetero)hydrocarbyl Diiron Complexes Mediated by the Interplay of Ligands

Ruthenium(II) Tris‐Pyrazolylmethane Complexes in Transfer Hydrogenation Reactions

The choice of μ-vinyliminium ligand substituents is key to optimize the antiproliferative activity of related diiron complexes

Collaborators (10)

Rita Mazzoni

Lorenzo Biancalana

Marcello Crucianelli

Stefano Zacchini

Tarita Biver

Gianluca Ciancaleoni

Gabriele Manca

GUIDO PAMPALONI

Valentina Gandin

Zdeněk Dvořák

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