A heterogeneous nickel-supported catalyst: a circular approach to amine synthesis via azide and nitro compound reduction

  • Filippo Campana
  • , Filippo Bocerani
  • , Federica Valentini
  • , Davide Gandolfo
  • , Dario Marchionni
  • , Dmitri Gelman
  • , Luigi Vaccaro*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The development of sustainable catalytic methods is a crucial tool for advancing green chemistry and reducing its associated environmental impact. In this study, we present an eco-friendly approach for reducing azido and nitro compounds to their corresponding amines using a heterogeneous nickel-based catalyst supported on sulfonated biochar derived from pine needle (PiNe) valorisation. The system developed, in combination with the use of NaBH4 as a safer reducing agent in water, enables efficient transformations under mild reaction conditions, yielding excellent results. The process also incorporates a green work-up procedure that employs bio-based, non-toxic solvents, such as 2-MeTHF, to aid in product isolation and catalyst recovery, thereby significantly reducing waste generation. Moreover, recycling studies demonstrate that Ni(B)/PiNe retains its catalytic efficiency for over five consecutive cycles. This work highlights the potential of biomass-derived materials in sustainable catalysis, demonstrating that green alternatives can be as effective as traditional methods while providing a protocol that aligns with the growing demand for environmentally friendly chemistry.

Original languageEnglish
Pages (from-to)5594-5600
Number of pages7
JournalRSC Sustainability
Volume3
Issue number12
DOIs
StatePublished - 15 Oct 2025

Bibliographical note

Publisher Copyright:
This journal is © The Royal Society of Chemistry

Fingerprint

Dive into the research topics of 'A heterogeneous nickel-supported catalyst: a circular approach to amine synthesis via azide and nitro compound reduction'. Together they form a unique fingerprint.

Cite this