Models of the iron-only hydrogenase: Synthesis and protonation of bridge and chelate complexes [Fe2(CO)4{Ph2P(CH2)nPPh2}(μ-pdt)] (n=2–4) – evidence for a terminal hydride intermediate
Author:
Publisher
Elsevier BV
Subject
General Chemical Engineering,General Chemistry
Reference11 articles.
1. De Novo Design of Synthetic Di-Iron(I) Complexes as Structural Models of the Reduced Form of Iron−Iron Hydrogenase
2. Synthesis, crystal structure and protonation of the asymmetric iron-only hydrogenase model [Fe2(CO)3(μ-pdt){μ,η2-Ph2PCH2CH2P(Ph)CH2CH2PPh2}] (pdt=SCH2CH2CH2S)
3. Models of the iron-only hydrogenase: Structural studies of chelating diphosphine complexes [Fe2(CO)4(µ-pdt)(κ2P,P′-diphosphine)]
4. Models of the iron-only hydrogenase: Reactions of [Fe2(CO)6(μ-pdt)] with small bite-angle diphosphines yielding bridge and chelate diphosphine complexes [Fe2(CO)4(diphosphine)(μ-pdt)]
5. Chelate Control of Diiron(I) Dithiolates Relevant to the [Fe−Fe]- Hydrogenase Active Site
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1. Homo and heteromultimetallic complexes containing a group 8 transition metal and μ-diphosphine bridging ligands involved in anticancer research: A review;European Journal of Medicinal Chemistry;2024-08
2. Synthesis of phosphine derivatives of [Fe2(CO)6(μ-sdt)] (sdt = SCH2SCH2S) and investigation of their proton reduction capabilities;Journal of Inorganic Biochemistry;2023-09
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4. Biomimics of [FeFe]-hydrogenases with a pendant amine: Diphosphine complexes [Fe2(CO)4{µ-S(CH2)nS}{κ2-(Ph2PCH2)2NR}] (n = 2, 3; R = Me, Bn) towards H2 oxidation catalysts;Journal of Organometallic Chemistry;2023-06
5. Bulky oxadithiolate-bridged [FeFe]‑hydrogenase mimics [Fe2(μ-R2odt)(CO)4(κ-diphosphine)] (R = Ph and H) with chelating diphosphines;Journal of Inorganic Biochemistry;2022-10
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