We demonstrate the formation of both metallo-organic crystals nanoscale films that have entirely different compositions and structures despite using the same set of starting materials. This difference is the result of an unexpected cation exchange process. The reaction of an iron polypyridyl complex with a copper salt by diffusion of one solution into another resulted in iron-to-copper exchange, concurrent ligand rearrangement, and the formation of metal-organic frameworks (MOFs). This observation shows that polypyridyl complexes can be used as expendable precursors for the growth of MOFs. In contrast, alternative depositions of the iron polypyridyl complex with a copper salt by automated spin coating on conductive metal oxides resulted in the formation of electrochromic coatings, and the structure and redox properties of the iron complex were retained. The possibility to form such different networks from the same set of molecular building blocks by "in solution" versus "on surface" coordination chemistry broadens the synthetic space to design functional materials.
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http://dx.doi.org/10.1021/jacs.1c08087 | DOI Listing |
J Biol Inorg Chem
December 2024
Department of Biology, Maynooth University, Maynooth, Co. Kildare, Ireland.
Infections caused by the airborne fungal pathogen, Aspergillus fumigatus, are increasing in severity due to growing numbers of immunocompromised individuals and the increasing incidence of antifungal drug resistance, exacerbating treatment challenges. Gallium has proven to be a strong candidate in the fight against microbial pathogens due to its iron-mimicking capability and substitution of Ga(III) in place of Fe(III), disrupting iron-dependent pathways. Since the antimicrobial properties of 2,2'-bipyridine and derivatives have been previously reported, we assessed the in vitro activity and proteomic effects of a recently reported heteroleptic Ga(III) polypyridyl catecholate compound against A.
View Article and Find Full Text PDFJ Inorg Biochem
November 2024
Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747, AG, Groningen, the Netherlands. Electronic address:
Redox non-innocent ligands hold the potential to expand the redox chemistry and activity of transition metal catalysts. The impact of the additional redox chemistry of phenol ligands in oxidation catalysis is explored here in the complex μ-oxido-diiron(III) polypyridyl (1) [(L)Fe(III)(μ-O)Fe(III)(L)](ClO) (where HL is 2-(((di(pyridin-2-yl)methyl) (pyridin-2-ylmethyl) amino)methyl)phenol) and its tert-butyl substituted analog 2, in which each of the Fe(III) centers is coordinated to a phenolato moiety of the ligand. Complex 1 was shown earlier to catalyse the oxidation of benzyl alcohols to aldehydes with HO.
View Article and Find Full Text PDFAcc Chem Res
February 2024
Université de Lorraine, CNRS, L2CM, F-54000 Nancy, France.
ConspectusThe harvesting and conversion of solar energy have become a burning issue for our modern societies seeking to move away from the exploitation of fossil fuels. In this context, dye-sensitized solar cells (DSSCs) have proven to be trustworthy alternatives to silicon-based cells with advantages in terms of transparency and efficiency under low illumination conditions. These devices are highly dependent on the ability of the sensitizer that they contain to collect sunlight and transfer an electron to a semiconductor after excitation.
View Article and Find Full Text PDFACS Catal
November 2023
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Molecular ammonia oxidation (AO) catalysis is a rapidly evolving research area. Among the catalysts studied, featuring metals including ruthenium, iron, manganese, nickel, and copper, polypyridyl iron complexes are attractive owing to fast catalytic rates and significant turnover numbers (TON). Building upon our previous work on AO using [(TPA)Fe(MeCN)] and [(BPM)Fe(MeCN)], this study investigates factors that impact rate and TON within and across catalyst series based on polypyridyl ligand frameworks.
View Article and Find Full Text PDFOrg Lett
October 2023
Department of Applied Chemistry, Kyung Hee University, Yongin 17104, Korea.
The oxidative alkenylation reaction of α-aminoalkyl C(sp)-H bonds has been investigated with ()-1,2-bis(sulfonyl)ethenes. The catalytic process of iron-polypyridyl complexes drives the single-electron oxidation of dialkyl anilines, resulting in the formation of α-aminoalkyl radical species. Subsequent cascades of radical addition and elimination reactions ensue, ultimately leading to the generation of sulfonylated allylic amine products.
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