A new dissymmetrically disubstituted diiron dithiolate species, [Fe(2)(CO)(4)(κ(2)-P(Ph)(2)N(Ph)(2))(μ-pdt)] (pdt = S(CH(2))(3)S), was prepared by using a flexible cyclic base-containing diphosphine, 1,3,5,7-tetraphenyl 1,5-diaza-3,7-diphosphacyclooctane (P(Ph)(2)N(Ph)(2) = {PhPCH(2)NPh}(2)). Preliminary investigations of proton and electron transfers on the diiron system have been done.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/c0cc03295f | DOI Listing |
Chem Biol Interact
November 2024
University of Pisa, Department of Chemistry and Industrial Chemistry, Via Giuseppe Moruzzi 13, I-56124, Pisa, Italy. Electronic address:
The new diiron complexes [FeCp(CO)(L)(μ-CO){μ-CN(Me)(Cy)}]CFSO (L = pyridine, 3a; 4-aminopyridine, 3b; 4-dimethylaminopyridine, 3c; 4-trifluoromethylpyridine, 3d; nicotinic acid, 4; Cp = η-CH, Cy = CH = cyclohexyl) were synthesized in moderate to high yields using two distinct synthetic routes from the precursors 1 (L = CO, for 4) and 2 (L = NCMe, for 3a-d), respectively. All products were characterized by IR and multinuclear NMR spectroscopy, and the structures of 3b and 3d were ascertained by X-ray diffraction studies. The behavior of the complexes in aqueous solutions (solubility, Log P, stability) was assessed using NMR and UV-Vis methods.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Carbon monoxide inhibited forms of nitrogenases have carbonyl (CO) and carbide (C) bridges, which are common in synthetic iron complexes with strong-field ligand environments but rare in iron sites with weak-field ligand environments analogous to the enzyme. Here, we explore the fundamental bonding description of bridging CO in high-spin iron systems. We describe the isolation of several diiron carbonyls and related species, and elucidate their electronic structures, magnetic coupling, and characteristic structural and vibrational parameters.
View Article and Find Full Text PDFChembiochem
November 2024
Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, China.
Dalton Trans
November 2024
State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Dalian University of Technology, Dalian 116024, P. R. China.
Thiolate-bridged bimetallic complexes have attracted considerable attention owing to their extensive applications in bioinspired catalysis as biological metalloenzymes. Compared with bimetallic complexes supported by common thiolate ligands, those featuring functional groups that may adopt different patterns to coordinate to the metal centers are usually difficult to access, limiting their exploration. The benzimidazole moiety is a multi-faceted functional group; for example, it can act as a biomolecule-responsive ligand for the development of transition metal complexes with anticancer and antitumor properties.
View Article and Find Full Text PDFChem Sci
October 2024
Department of Biochemistry and Biophysics, Stockholm University Stockholm 10691 Sweden
The alternative oxidase (AOX) is a membrane-bound di-iron enzyme that catalyzes O-driven quinol oxidation in the respiratory chains of plants, fungi, and several pathogenic protists of biomedical and industrial interest. Yet, despite significant biochemical and structural efforts over the last decades, the catalytic principles of AOX remain poorly understood. We develop here multi-scale quantum and classical molecular simulations in combination with biochemical experiments to address the proton-coupled electron transfer (PCET) reactions responsible for catalysis in AOX from , the causative agent of sleeping sickness.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!