Catalysts for nitrogen reduction to ammonia

SL Foster, SIP Bakovic, RD Duda, S Maheshwari… - Nature Catalysis, 2018 - nature.com
The production of synthetic ammonia remains dependent on the energy-and capital-
intensive Haber–Bosch process. Extensive research in molecular catalysis has …

Metal–Sulfur Compounds in N2 Reduction and Nitrogenase-Related Chemistry

K Tanifuji, Y Ohki - Chemical reviews, 2020 - ACS Publications
Transition metal–sulfur (M–S) compounds are an indispensable means for biological
systems to convert N2 into NH3 (biological N2 fixation), and these may have emerged by …

Insight into the iron–molybdenum cofactor of nitrogenase from synthetic iron complexes with sulfur, carbon, and hydride ligands

I Čorić, PL Holland - Journal of the American Chemical Society, 2016 - ACS Publications
Nitrogenase enzymes are used by microorganisms for converting atmospheric N2 to
ammonia, which provides an essential source of N atoms for higher organisms. The active …

Terminal Hydride Complex of High-Spin Mn

A Drena, A Fraker, NB Thompson… - Journal of the …, 2024 - ACS Publications
The iron–molybdenum cofactor of nitrogenase (FeMoco) catalyzes fixation of N2 via Fe
hydride intermediates. Our understanding of these species has relied heavily on the …

Hydrogen atom abstraction by a high-spin [FeIII= S] complex

JA Valdez-Moreira, DC Wannipurage, M Pink, V Carta… - Chem, 2023 - cell.com
Iron-sulfur clusters are critical to a plethora of biological processes; however, little is known
about the elementary unit of these clusters, namely, the [Fe= S] n+ fragment. Here, we report …

Isostructural bridging diferrous chalcogenide cores [Fe II (μ-E) Fe II](E= O, S, Se, Te) with decreasing antiferromagnetic coupling down the chalcogenide series

E Zars, L Gravogl, MR Gau, PJ Carroll, K Meyer… - Chemical …, 2023 - pubs.rsc.org
Iron compounds containing a bridging oxo or sulfido moiety are ubiquitous in biological
systems, but substitution with the heavier chalcogenides selenium and tellurium, however, is …

Activation of an open shell, carbyne-bridged diiron complex toward binding of dinitrogen

CH Arnett, T Agapie - Journal of the American Chemical Society, 2020 - ACS Publications
Binding of N2 by nitrogenase requires a reductive activation of the FeMo-cofactor, but the
precise structure and atomic composition of FeMoco in its activated form is not well …

Structure, reactivity, and spectroscopy of nitrogenase-related synthetic and biological clusters

CH Wang, S DeBeer - Chemical Society Reviews, 2021 - pubs.rsc.org
The reduction of dinitrogen (N2) is essential for its incorporation into nucleic acids and
amino acids, which are vital to life on earth. Nitrogenases convert atmospheric dinitrogen to …

Low-Coordinate Iron Hydride Chemistry at an N, N, C-Heteroscorpionate Platform

A Fraker, BN Linn, A McSkimming - Inorganic Chemistry, 2024 - ACS Publications
Locally high-spin iron hydrides are proposed to play a critical role as intermediates in iron–
molybdenum cofactor (FeMoco)-catalyzed N2 fixation. Inspired by these biological systems …

Water-catalyzed iron-molybdenum carbyne formation in bimetallic acetylene transformation

X Zhai, M Xue, Q Zhao, Q Zheng, D Song… - Nature …, 2024 - nature.com
Transition metal carbyne complexes are of fundamental importance in carbon-carbon bond
formation, alkyne metathesis, and alkyne coupling reactions. Most reported iron carbyne …