We report a survey of the reactivity of the first isolable iron-hydride complexes with a coordination number less than 5. The high-spin iron(II) complexes [(beta-diketiminate)Fe(mu-H)] 2 react rapidly with representative cyanide, isocyanide, alkyne, N 2, alkene, diazene, azide, CO 2, carbodiimide, and Brønsted acid containing substrates. The reaction outcomes fall into three categories: (1) addition of Fe-H across a multiple bond of the substrate, (2) reductive elimination of H 2 to form iron(I) products, and (3) protonation of the hydride to form iron(II) products. The products include imide, isocyanide, vinyl, alkyl, azide, triazenido, benzo[ c]cinnoline, amidinate, formate, and hydroxo complexes. These results expand the range of known bond transformations at iron complexes. Additionally, they give insight into the elementary transformations that may be possible at the iron-molybdenum cofactor of nitrogenases, which may have hydride ligands on high-spin, low-coordinate metal atoms.
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http://dx.doi.org/10.1021/ja710669w | DOI Listing |
Inorg Chem
August 2024
Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, United States.
Locally high-spin iron hydrides are proposed to play a critical role as intermediates in iron-molybdenum cofactor (FeMoco)-catalyzed N fixation. Inspired by these biological systems, we report herein our initial investigations into low-coordinate iron hydride chemistry supported by our N,N,C-heteroscorpionate ligands. Those ligands with smaller steric profiles are unable to completely suppress the formation of a binuclear [Fe(μ-H)] complex; however, the incorporation of more substantial steric bulk allows for the isolation of a rare example of a terminal, high-spin ( = 2) Fe hydride.
View Article and Find Full Text PDFJ Am Chem Soc
July 2024
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.
We report on the use of a simple, bench-stable [Fe(salen)]-μ-oxo precatalyst in the reduction of nitro compounds. The reaction proceeds at room temperature across a range of substrates, including nitro aromatics and aliphatics. By changing the reducing agent from pinacol borane (HBpin) to phenyl silane (HSiPh), we can chemoselectively reduce nitro compounds while retaining carbonyl functionality.
View Article and Find Full Text PDFJ Am Chem Soc
July 2024
Department of Chemistry, University of California, Irvine, California 92697-2025, United States.
Directed hydrogen atom transfer to alkenes is described. The process is catalyzed by iron complexes and allows for the site-selective hydrofunctionalization of polyenols. Experimental data suggest that coordination of the hydroxy group to the iron hydride intermediate plays an important role in preferential engagement of the allylic alcohol motif and provides a new basis for selectivity in radical hydrofunctionalization events.
View Article and Find Full Text PDFInorg Chem
January 2023
Department of Chemistry, University of Cincinnati, P.O. Box 210172, Cincinnati, Ohio45221-0172, United States.
Iron dihydride complexes are key intermediates in many iron-catalyzed reactions. Previous efforts to study molecules of this type have led to the discovery of a remarkably stable -FeH complex, which is supported by bis[2-(diisopropylphosphino)phenyl]phosphine (PPP) along with CO. In this work, the hydrogen on the central phosphorus has been replaced with a methyl group, and the corresponding iron carbonyl dichloride, hydrido chloride, and dihydride complexes have been synthesized.
View Article and Find Full Text PDFInorg Chem
January 2023
Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan.
Continued efforts are made on the development of earth-abundant metal catalysts for dehydrogenation/hydrolysis of amine boranes. In this study, complex [K-18-crown-6-ether][(NO)Fe(μ-Pyr)(μ-CO)Fe(NO)] (, Pyr = 3-methylpyrazolate) was explored as a pre-catalyst for the dehydrogenation of dimethylamine borane (DMAB). Upon evolution of H from DMAB triggered by , parallel conversion of into [(NO)Fe(,'-PyrBHNMe)] () and an iron-hydride intermediate [(NO)(CO)Fe(μ-H)Fe(CO)(NO)] () was evidenced by X-ray diffraction/nuclear magnetic resonance/infrared/nuclear resonance vibrational spectroscopy experiments and supported by density functional theory calculations.
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