Djihed Boucherabine
Djihed Boucherabine
ORCID: https://orcid.org/0009-0008-6907-6579
Dr. Djihed Boucherabine, Ph.D, is an esteemed researcher in the field of Electrochemical Engineering, with a specialization that seamlessly blends organic and inorganic chemistry. He earned his doctorate focusing on catalytic epoxidation of alkenes using Metal Schiff bases complexes. After completing his Ph.D, dr. Boucherabine joined the University of Milan as a postdoctoral researcher, where he delves into photochemistry and catalysis involving the use of pyclen ligands and their metal complexes under the supervision of Prof. Alessandro Caselli. His research endeavors also include studying the catalytic cycloaddition of carbon dioxide to Phenol Glycidate substrates for the upscaling of waste chemicals. Dr. Boucherabine’s areas of expertise span the synthesis of new transition metal complexes, various spectroscopy techniques, electrochemistry. He also has a specialized focus on DFT and TD-DFT calculations, particularly in linear and nonlinear optical properties.
Publications
2026
Alberti, Matteo; Rossi, Greta; Boucherabine, Djihed; Cargnoni, Fausto; Trioni, Mario Italo; Taini, Giulia; Zakutna, Dominika; Gentilin, Arianna; Đorđević, Luka; Sartorel, Andrea; Caselli, Alessandro
Photoactive Fe(
In: Dalton Trans., 2026, ISSN: 1477-9234.
@article{Alberti2026,
title = {Photoactive Fe(
iii
) pyclen complexes for light-driven aerobic oxidation of
\textit{p}
-xylene},
author = {Matteo Alberti and Greta Rossi and Djihed Boucherabine and Fausto Cargnoni and Mario Italo Trioni and Giulia Taini and Dominika Zakutna and Arianna Gentilin and Luka Đorđević and Andrea Sartorel and Alessandro Caselli},
doi = {10.1039/d5dt02534f},
issn = {1477-9234},
year = {2026},
date = {2026-00-00},
journal = {Dalton Trans.},
publisher = {Royal Society of Chemistry (RSC)},
abstract = {
We report the photochemical activity of iron coordination complexes with pyclen and bromide ligands, in generating bromine radicals, exploited for the aerobic oxidation of
p
-xylene under visible light.
},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
We report the photochemical activity of iron coordination complexes with pyclen and bromide ligands, in generating bromine radicals, exploited for the aerobic oxidation of
-xylene under visible light.
2025
Alberti, Matteo; Gianelli, Marta; Boucherabine, Djihed; Recchia, Sandro; Caselli, Alessandro
Additive‐Free Synthesis of Cyclic Carbamates From Aziridines and CO2 Catalyzed by IER Supported Iron(III) Halides Journal Article
In: ChemCatChem, 2025, ISSN: 1867-3899.
@article{Alberti2025,
title = {Additive‐Free Synthesis of Cyclic Carbamates From Aziridines and CO_{2} Catalyzed by IER Supported Iron(III) Halides},
author = {Matteo Alberti and Marta Gianelli and Djihed Boucherabine and Sandro Recchia and Alessandro Caselli},
doi = {10.1002/cctc.202500710},
issn = {1867-3899},
year = {2025},
date = {2025-07-24},
journal = {ChemCatChem},
publisher = {Wiley},
abstract = {Abstract The coupling of CO2 with aziridines offers an efficient, 100% atom‐economic route to synthesize high‐value cyclic carbamates. In this study, we present a heterogeneous catalytic system based on readily available iron(III) metallates supported on commercially available ion‐exchange resins (IERs) for the selective synthesis of 1,3‐oxazolidin‐2‐ones. Two polystyrene‐based IERs with different porosities, Amberlyst™ 26‐Cl (A26‐Cl, macroreticular) and Amberlite™ IRA‐400‐Cl (IRA400‐Cl, microporous) were evaluated. The results reveal a synergistic interaction between the iron metallate and the resin support, with the A26‐[FeCl3 Br] catalyst outperforming the homogeneous counterpart under mild conditions (25 °C, CO2 pressure = 0.8 MPa, 2 h), achieving up to >99% yield of the target oxazolidinone. A Design of Experiments (DoE) approach was applied to optimize reaction parameters, and the system's versatility was confirmed using aziridines with different substitution patterns. Overall, this work presents a scalable (up to 1 g) and cost‐effective method for CO2 valorization into cyclic carbamates, highlighting experimentally the combined effect of polystyrene supports and ammonium ferrate active species. },
keywords = {},
pubstate = {published},
tppubtype = {article}
}