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

被引:0
|
作者
Benndorf, Stefan [1 ]
Groni, Sihem [2 ]
Stafast, Leanne M. [1 ]
Gorls, Helmar [1 ]
Fave, Claire [2 ]
Schollhorn, Bernd [2 ]
Weigand, Wolfgang [1 ,3 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Inorgan & Analyt Chem, Humboldtstr 8, D-07743 Jena, Germany
[2] Univ Paris Cite, Lab Electrochim Mol, F-75013 Paris, France
[3] Friedrich Schiller Univ Jena, Ctr Energy & Environm Chem Jena CEEC Jena, Jena Ctr Soft Matter, Philosophenweg 7a, D-07743 Jena, Germany
关键词
cyclic voltammetry; electrode modification; FeFe] hydrogenase mimics; monolayers; spectroelectrochemistry; DIRECT-ELECTRON-TRANSFER; ACTIVE-SITE; PROTON-REDUCTION; ELECTROCHEMICAL PROPERTIES; DIIRON PROPANEDITHIOLATE; MOLECULAR-STRUCTURES; COVALENT ATTACHMENT; ONLY HYDROGENASE; MODEL COMPLEXES; H-2; EVOLUTION;
D O I
10.1002/ejic.202200684
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
[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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页数:10
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