Synthetic and structural studies of dicobalt–iron complexes with intramolecular bridging bidentate ligands
Author:
Affiliation:
1. Department of Chemical Engineering, Center of Analysis and Testing, Ningbo University of Technology, Ningbo, China
Publisher
Informa UK Limited
Subject
Materials Chemistry,Physical and Theoretical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00958972.2014.961443
Reference16 articles.
1. Models of the iron-only hydrogenase: a comparison of chelate and bridge isomers of Fe2(CO)4{Ph2PN(R)PPh2}(μ-pdt) as proton-reduction catalysts
2. Electron-Transfer-Catalyzed Rearrangement of Unsymmetrically Substituted Diiron Dithiolate Complexes Related to the Active Site of the [FeFe]-Hydrogenases
3. Hydrogenase biomimetics: Fe2(CO)4(μ-dppf)(μ-pdt) (dppf = 1,1′-bis(diphenylphosphino)ferrocene) both a proton-reduction and hydrogen oxidation catalyst
4. Substitution reactions of [FeFe]-hydrogenase model complexes containing diselenolate bridges
5. Synthesis and structural characterization of a diiron propanedithiolate complex [( μ -PDT)Fe2(CO)5]2[(η 5-Ph2PC5H4)2Fe] containing a bidentate phosphine ligand 1,1′-bis(diphenylphosphino)ferrocene
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