Issue 46, 2025

A tetradentate benzannulated P^N^N^P ligand and its Fe(ii) complex: synthesis, characterization, and electrocatalytic hydrogen evolution

Abstract

Iron complexes supported by phosphine and pyridine-based ligands are widely seen as efficient molecular catalysts for catalytic transformations, but examples of these complexes as molecular electrocatalysts for the hydrogen evolution reaction (HER) are limited. In this work, we present a ligand design based on a 6,6′-fused dimer of a 2,4-substituted (phosphino)phenanthridine (benzo[c]quinoline). Starting from the monomeric P^N precursor, we show how the P^N^N^P dimer can be selectively formed and report the synthesis and characterization of an Fe(II) complex of this unique scaffold. We demonstrate the potential of such frameworks in the electrocatalytic reduction of Brønsted acids in acetonitrile solution.

Graphical abstract: A tetradentate benzannulated P^N^N^P ligand and its Fe(ii) complex: synthesis, characterization, and electrocatalytic hydrogen evolution

Supplementary files

Article information

Article type
Paper
Submitted
13 Sep 2025
Accepted
24 Oct 2025
First published
30 Oct 2025
This article is Open Access
Creative Commons BY license

Dalton Trans., 2025,54, 17211-17220

A tetradentate benzannulated P^N^N^P ligand and its Fe(II) complex: synthesis, characterization, and electrocatalytic hydrogen evolution

B. K. Sidhu, A. Kacperkiewicz, J. D. Braun and D. E. Herbert, Dalton Trans., 2025, 54, 17211 DOI: 10.1039/D5DT02202A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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