Synthesis of [FeFe] Hydrogenase Mimics with Lipoic acid and its Selenium Analogue as Anchor Groups

GND
1317657837
ORCID
0000-0002-5305-848X
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena
Benndorf, Stefan;
ORCID
0000-0003-4655-3623
Zugehörigkeit
Université Paris Cité Laboratoire d'Electrochimie Moléculaire F-75013 Paris France
Groni, Sihem;
GND
1317777581
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena
Stafast, Leanne M.;
GND
1214845193
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena
Görls, Helmar;
ORCID
0000-0001-8146-8702
Zugehörigkeit
Université Paris Cité Laboratoire d'Electrochimie Moléculaire F-75013 Paris France
Fave, Claire;
ORCID
0000-0001-6446-8399
Zugehörigkeit
Université Paris Cité Laboratoire d'Electrochimie Moléculaire F-75013 Paris France
Schöllhorn, Bernd;
GND
1062586395
ORCID
0000-0001-5177-1006
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena
Weigand, Wolfgang

[FeFe] hydrogenase (H 2 ase) mimicking complexes containing lipoic and selenolipoic acid moieties connected to 2‐hydroxy‐1,3‐dithiopropane and 2‐hydroxy‐1,3‐diselenopropane bridging ligands were synthesized and characterized using different spectroscopic methods. X‐ray diffraction analysis was utilized to determine the molecular structure of a triphenylphosphane substituted analogue. Cyclic voltammetry (CV) investigations on the redox chemistry in presence and absence of acetic acid (AcOH) revealed differing behaviours among the mimics. IR spectroelectrochemistry (IR SEC) enabled deeper insights of structural changes during electrochemical measurements. The elaboration of surface confined systems was studied in preliminary experiments. CV experiments showed that the lipoic acid derivatives of the [FeFe] H 2 ase mimics formed well‐organized self‐assembled monolayers (SAMs) on Pt electrodes, a promising result for future work.

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