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  1. 101
    “…[FeFe]-hydrogenases efficiently catalyzes hydrogen conversion at a unique [4Fe–4S]-[FeFe] cofactor, the so-called H-cluster. …”
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    Spectroscopical Investigations on the Redox Chemistry of [FeFe]-Hydrogenases in the Presence of Carbon Monoxide
  2. 102
    “…[FeFe]-Hydrogenases are hydrogen producing metalloenzymes with excellent catalytic capacities, highly relevant in the context of a future hydrogen economy. …”
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    Generation of a functional, semisynthetic [FeFe]-hydrogenase in a photosynthetic microorganism
  3. 103
    “…[NiFeSe] hydrogenases are a subclass of [NiFe] hydrogenases with, usually, an increased insensitivity to aerobic environments. …”
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    Studying O(2) pathways in [NiFe]- and [NiFeSe]-hydrogenases
  4. 104
    “…For this purpose, the changes in the content of micronutrient ions and Fe-EDDHA and Fe-EDDHSA chelates in an aqueous medium at different pH values were studied. …”
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    Chemical Stability of the Fertilizer Chelates Fe-EDDHA and Fe-EDDHSA over Time
  5. 105
    “…A [Fe‐S‐Fe] subunit with a single sulfide bridging two low‐coordinate iron ions is the supposed active site of the iron‐molybdenum co‐factor (FeMoco) of nitrogenase. …”
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    A Molecular Low‐Coordinate [Fe‐S‐Fe] Unit in Three Oxidation States
  6. 106
    “…Here we constructed a new high-T(g) interface, single-layer FeSe interfaced with FeO(x)-terminated LaFeO(3). …”
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    High temperature superconductivity at FeSe/LaFeO(3) interface
  7. 107
    “…[Image: see text] [FeFe] hydrogenases are highly active enzymes for interconverting protons and electrons with hydrogen (H(2)). …”
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    The Nonphysiological Reductant Sodium Dithionite and [FeFe] Hydrogenase: Influence on the Enzyme Mechanism
  8. 108
    “…The [FeFe]-hydrogenases are enzymes that catalyze the reversible activation of H(2) coupled to the reduction–oxidation of electron carriers. …”
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    The Contribution of Proton-Donor pKa on Reactivity Profiles of [FeFe]-hydrogenases
  9. 109
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    Adsorbtion of oxygen, hydrogen, nitrogen, and $OH^-$ group on Fe, $FeO$, $Fe_2O_3$ and $SiO_2$ surfaces
  10. 110
    “…We investigate the interfacial chemistry of secondary Fe(2)O(3) phases formed in a BiFeO(3) (BFO) layer in BFO/ La(0.67)Sr(0.33)MnO(3) (LSMO)/SrTiO(3) (STO) heterostructures. …”
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    Chemistry of the Fe(2)O(3)/BiFeO(3) Interface in BiFeO(3) Thin Film Heterostructures
  11. 111
    “…[FeFe]-Hydrogenases catalyze the evolution and oxidation of hydrogen using a characteristic cofactor, termed the H-cluster. …”
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    Influence of the [4Fe–4S] cluster coordinating cysteines on active site maturation and catalytic properties of C. reinhardtii [FeFe]-hydrogenase
  12. 112
    “…Following the characterization, we validate virus infection for FeV1, FeV2 and FeV4 for the first time in field-collected worker ants. …”
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    Genome organization and molecular characterization of the three Formica exsecta viruses—FeV1, FeV2 and FeV4
  13. 113
    “…Chemical synthesis of the conducting polymer polypyrrole induced by [Fe(CN)(6)](3−) is reported. Reaction kinetics were characterized spectrophotometrically. …”
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    Synthesis of Polypyrrole Induced by [Fe(CN)(6)](3−) and Redox Cycling of [Fe(CN)(6)](4−)/[Fe(CN)(6)](3−)
  14. 114
    “…In this article, the Fe(3+)-sensitive carbon dots were obtained by means of a microwave-assisted method using glutamic acid and ethylenediamine as reactants. …”
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    Fe(3+)-Sensitive Carbon Dots for Detection of Fe(3+) in Aqueous Solution and Intracellular Imaging of Fe(3+) Inside Fungal Cells
  15. 115
    por Britt, R. David, Rao, Guodong, Tao, Lizhi
    Publicado 2020
    “…[FeFe] hydrogenases carry out the redox interconversion of protons and molecular hydrogen (2H(+) + 2e(−) ⇌ H(2)) at a complex Fe–S active site known as the H-cluster. …”
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    Biosynthesis of the catalytic H-cluster of [FeFe] hydrogenase: the roles of the Fe–S maturase proteins HydE, HydF, and HydG
  16. 116
    “…Diversity in relay design is exemplified among different members of hydrogenases, enzymes which catalyze reversible H(2) activation, which also couple to diverse types of donor and acceptor molecules. The [FeFe]-hydrogenase I from Clostridium acetobutylicum (CaI) is a member of a large family of structurally related enzymes where interfacial electron transfer is mediated by a terminal, non-canonical, His-coordinated, [4Fe–4S] cluster. …”
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    A site-differentiated [4Fe–4S] cluster controls electron transfer reactivity of Clostridium acetobutylicum [FeFe]-hydrogenase I
  17. 117
    “…Fe(II) and Fe(III) at the first (C(n)) and third (C(n+6)) cysteine ligand sites form a mixed-valence Fe(2.5+)···Fe(2.5+) pair in the reduced Fe(II)(3)Fe(III) cluster. …”
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    Mechanism of Mixed-Valence Fe(2.5+)···Fe(2.5+) Formation in Fe(4)S(4) Clusters in the Ferredoxin Binding Motif
  18. 118
    por Agoro, Mojeed A., Meyer, Edson L.
    Publicado 2022
    “…Nanoscale FeS and FeS(2) mixed phases were synthesized by one-pot decomposition of (N-anil-N-piperldtc)Fe1 as FeS#1), (N-piperldtc)Fe2 as FeS#2) and (N-anildtc)Fe3 as FeS#3) complexes as precursors, with the help of tri-n-octylphosphine oxide (TOPO) coordinating solvent. …”
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    FeS/FeS(2) nanoscale structures synthesized in one step from Fe(ll) dithiocarbamate complexes as a single source precursor
  19. 119
    “…Two sets of core/shell magnetic nanoparticles, CoFe(2)O(4)/Fe(3)O(4) and Fe(3)O(4)/CoFe(2)O(4), with a fixed diameter of the core (~ 4.1 and ~ 6.3 nm for the former and latter sets, respectively) and thickness of shells up to 2.5 nm were synthesized from metal chlorides in a diethylene glycol solution. …”
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    Profound Interfacial Effects in CoFe(2)O(4)/Fe(3)O(4) and Fe(3)O(4)/CoFe(2)O(4) Core/Shell Nanoparticles
  20. 120
    “…The over-oxidation did not happen in the UV/Fe(II)/S(IV) pretreatment, which may be attributed to the cyclic redox Fe(II)/Fe(III) coagulation triggered by the Fe(II). …”
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    UV/Fe(II)/S(IV) Pretreatment for Ultrafiltration of Microcystis aeruginosa-Laden Water: Fe(II)/Fe(III) Triggered Synergistic Oxidation and Coagulation
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