All Stories

  1. Unlocking a Simpler Path to Nitrogen Fixation
  2. Ancient nitrogenases are ATP dependent
  3. The Origins of ATP Dependence in Biological Nitrogen Fixation
  4. Low-temperature trapping of N2 reduction reaction intermediates in nitrogenase MoFe protein–CdS quantum dot complexes
  5. High Affinity Electrostatic Interactions Support the Formation of CdS Quantum Dot:Nitrogenase MoFe Protein Complexes
  6. Cryo-annealing of Photoreduced CdS Quantum Dot–Nitrogenase MoFe Protein Complexes Reveals the Kinetic Stability of the E4(2N2H) Intermediate
  7. The Fe Protein Cycle Associated with Nitrogenase Catalysis Requires the Hydrolysis of Two ATP for Each Single Electron Transfer Event
  8. A conformational equilibrium in the nitrogenase MoFe protein with an α-V70I amino acid substitution illuminates the mechanism of H2 formation
  9. 13C ENDOR Characterization of the Central Carbon within the Nitrogenase Catalytic Cofactor Indicates That the CFe6Core Is a Stabilizing “Heart of Steel”
  10. The One-Electron Reduced Active-Site FeFe-Cofactor of Fe-Nitrogenase Contains a Hydride Bound to a Formally Oxidized Metal-Ion Core
  11. Exploring the Role of the Central Carbide of the Nitrogenase Active-Site FeMo-cofactor through Targeted13C Labeling and ENDOR Spectroscopy
  12. The electronic structure of FeV-cofactor in vanadium-dependent nitrogenase
  13. Electron Redistribution within the Nitrogenase Active Site FeMo-Cofactor During Reductive Elimination of H2 to Achieve N≡N Triple-Bond Activation
  14. Correction to “Establishing a Thermodynamic Landscape for the Active Site of Mo-Dependent Nitrogenase”
  15. Reduction of Substrates by Nitrogenases
  16. An Efficient Viologen-Based Electron Donor to Nitrogenase
  17. Establishing a Thermodynamic Landscape for the Active Site of Mo-Dependent Nitrogenase
  18. Spectroscopic Description of the E1State of Mo Nitrogenase Based on Mo and Fe X-ray Absorption and Mössbauer Studies
  19. Mo-, V-, and Fe-Nitrogenases Use a Universal Eight-Electron Reductive-Elimination Mechanism To Achieve N2Reduction
  20. (Invited) Electrocatalytic N2 Reduction to NH3 Using the Enzyme Nitrogenase
  21. A Voltammetric Study of Nitrogenase Catalysis Using Electron Transfer Mediators
  22. Kinetic Understanding of N2Reduction versus H2Evolution at the E4(4H) Janus State in the Three Nitrogenases
  23. Hydride Conformers of the Nitrogenase FeMo-cofactor Two-Electron Reduced State E2(2H), Assigned Using Cryogenic Intra Electron Paramagnetic Resonance Cavity Photolysis
  24. A pathway for biological methane production using bacterial iron-only nitrogenase
  25. Light-driven carbon dioxide reduction to methane by nitrogenase in a photosynthetic bacterium
  26. Reductive Elimination of H2 Activates Nitrogenase to Reduce the N≡N Triple Bond: Characterization of the E4(4H) Janus Intermediate in Wild-Type Enzyme
  27. Exploring Electron/Proton Transfer and Conformational Changes in the Nitrogenase MoFe Protein and FeMo-cofactor Through Cryoreduction/EPR Measurements
  28. Evidence That the Pi Release Event Is the Rate-Limiting Step in the Nitrogenase Catalytic Cycle
  29. Reversible Photoinduced Reductive Elimination of H2 from the Nitrogenase Dihydride State, the E4(4H) Janus Intermediate
  30. Identification of a Key Catalytic Intermediate Demonstrates That Nitrogenase Is Activated by the Reversible Exchange of N2 for H2
  31. A Confirmation of the Quench-Cryoannealing Relaxation Protocol for Identifying Reduction States of Freeze-Trapped Nitrogenase Intermediates
  32. Mechanism of Nitrogen Fixation by Nitrogenase: The Next Stage
  33. On reversible H 2 loss upon N 2 binding to FeMo-cofactor of nitrogenase
  34. Nitrogenase reduction of carbon-containing compounds
  35. Carbon dioxide reduction to methane and coupling with acetylene to form propylene catalyzed by remodeled nitrogenase
  36. The Nitrogenase Regulatory Enzyme Dinitrogenase Reductase ADP-Ribosyltransferase (DraT) Is Activated by Direct Interaction with the Signal Transduction Protein GlnB
  37. Unification of reaction pathway and kinetic scheme for N 2 reduction catalyzed by nitrogenase
  38. ENDOR/HYSCORE Studies of the Common Intermediate Trapped during Nitrogenase Reduction of N2H2, CH3N2H, and N2H4Support an Alternating Reaction Pathway for N2Reduction
  39. Molybdenum Nitrogenase Catalyzes the Reduction and Coupling of CO to Form Hydrocarbons*
  40. Steric Control of the Hi‐CO MoFe Nitrogenase Complex Revealed by Stopped‐Flow Infrared Spectroscopy
  41. Is Mo Involved in Hydride Binding by the Four-Electron Reduced (E4) Intermediate of the Nitrogenase MoFe Protein?
  42. Synthesis and Characterization of Diiron Thiadithiolate Complexes Related to the Active Site of [FeFe]-Hydrogenases
  43. Synthesis and structural characterization of the mono- and diphosphine-containing diiron propanedithiolate complexes related to [FeFe]-hydrogenases. Biomimetic H2 evolution catalyzed by (μ-PDT)Fe2(CO)4[(Ph2P)2N(n-Pr)]
  44. Synthesis, Structural Characterization, and Some Properties of New N-Functionally Substituted Diiron Azadithiolate Complexes as Biomimetic Models of Iron-Only Hydrogenases
  45. Diiron Thiadithiolates as Active Site Models for the Iron-Only Hydrogenases:  Synthesis, Structures, and Catalytic H2Production
  46. Diiron Oxadithiolate Type Models for the Active Site of Iron-Only Hydrogenases and Biomimetic Hydrogen Evolution Catalyzed by Fe2(μ-SCH2OCH2S-μ)(CO)6
  47. Novel Single and Double Diiron Oxadithiolates as Models for the Active Site of [Fe]-Only Hydrogenases
  48. Formation and Chemical Reactivities of a New Type of Double-Butterfly [{Fe2(-CO)(CO)6}2(-SZS-)]2: Synthetic and Structural Studies on Novel Linear and Macrocyclic Butterfly Fe/E (E=S, Se) Cluster Complexes
  49. Reactions of Butterfly Complex Anions of the Type [(μ-RTe)(μ-CO)Fe2(CO)6]-with Electrophiles. A New Route toμ4-Se-Containing Double-Butterfly Clusters. Crystal Structures of (μ-p-MeC6H4Te)(μ-PhCH2SCS)Fe2(CO)6and [(μ-RTe)Fe2(CO)6]2(μ4-Se) (R = Ph,p-BrC6H4)