A convenient ligand exchange pathway to [2Fe-2S] ferredoxin analogues

2009 | journal article. A publication with affiliation to the University of Göttingen.

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​A convenient ligand exchange pathway to [2Fe-2S] ferredoxin analogues​
Ballmann, J.; Sun, X.; Dechert, S. ; Schneider, B. & Meyer, F.​ (2009) 
Dalton Transactions,(25) pp. 4908​-4917​.​ DOI: https://doi.org/10.1039/b901242g 

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Authors
Ballmann, Joachim; Sun, Xianru; Dechert, Sebastian ; Schneider, Benjamin; Meyer, Franc
Abstract
The benzanellated analogues (NEt(4))(2)[Fe(2)S(2)(indolate)(4)] (2) and (NEt(4))(2)[Fe(2)S(2)(carbazolate)(4)] (3) of the previously reported parent (NEt(4))(2)[Fe(2)S(2)(pyrrolate)(4)] cluster (1) were synthesized and characterized spectroscopically. In contrast to 1 and 3, compound 2 can be applied as a versatile precursor in ligand exchange reactions with various thiophenols affording the thiophenolate-coordinate [2Fe-2S] clusters. Heteroaromatic thiols and chelating biphenols are suitable substrates in this conversion as well, providing a convenient access to a variety of new [2Fe-2S] ferredoxin analogues and related complexes. Several new S- and O-coordinate [2Fe-2S] clusters have been prepared and fully characterized, including five X-ray crystal structures.
Issue Date
2009
Status
published
Publisher
Royal Soc Chemistry
Journal
Dalton Transactions 
ISSN
1477-9226
Sponsor
DFG

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