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Evidence for the Formation of Terminal Hydrides by Protonation of an Asymmetric Iron Hydrogenase Active Site Mimic

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Evidence_for_the_Formation_of_Terminal_Hydrides_by_Protonation_of_an_Asymmetric_Iron_Hydrogenase_Active_Site_Mimic/3010570
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Treatment of [Fe2(μ-pdt)(CO)6] [pdt = S(CH2)3S] with dppe (Ph2PCH2CH2PPh2) in refluxing toluene affords the asymmetric complex [Fe2(μ-pdt)(CO)4(dppe)] (1). Protonation of 1 with HBF4−Et2O in CH2Cl2 gives at room temperature the μ-hydrido derivative [Fe2(μ-pdt)(CO)4(dppe)(μ-H)](BF4) (2). Monitoring the reaction by 1H, 31P, and 13C NMR at low temperature reveals unambiguously that the process of the protonation of 1 implies terminal hydride intermediates.
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2016-06-03
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