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Integrating radical (open-shell) species into non-cryogenic nanodevices is key to unlocking the potential of molecular electronics. While many efforts have been devoted to this issue, in the absence of a chemical/electrochemical potential the open-shell character is generally lost in contact with the metallic electrodes. Herein, single-molecule devices incorporating a 6-oxo-verdazyl persistent radical have been fabricated using break-junction techniques. The open-shell character is retained at room temperature, and electrochemical gating permits in situ reduction to a closed-shell anionic state in a single-molecule transistor configuration. Furthermore, electronically driven rectification arises from bias-dependent alignment of the open-shell resonances. The integration of radical character, transistor-like switching, and rectification in a single molecular component paves the way to further studies of the electronic, magnetic, and thermoelectric properties of open-shell species.
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http://dx.doi.org/10.1002/anie.202116985 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 276, 69120, Heidelberg, Germany.
Dinuclear M(I)-M(I) complexes (M = Ni, Pd) may serve as stable reservoir forms for highly reactive mononuclear metalloradicals, which are of interest as potential catalytic species. However, their dissociation dynamics as well as the factors governing monomer stabilization remain incompletely understood. This study investigates the influence of steric bulk and residual ligand flexibility within a PNP pincer framework on the homolytic dissociation behavior of unsupported Ni(I)-Ni(I) and Pd(I)-Pd(I) dimers.
View Article and Find Full Text PDFChem Commun (Camb)
August 2025
Department of Chemistry, Philipps-University Marburg, Hans-Meerwein-Str. 4, D-35037 Marburg, Germany.
Linear 3d-metal complexes with open-shell metal ions have fascinated coordination chemists for decades. Originally the focus was on metal(II) species, yet the synthetic possibilities to acquire their reduced analogues, together with the introduction of NHCs as stabilizing co-ligands, have expanded the structural knowledge and feasible oxidation states to +I and even 0. Despite a certain wealth of structural data, insights into the reactivity or even catalytic applications of such compounds remained comparably thin for a long time given the intrinsic lability of these coordinatively and electronically unsaturated compounds.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States.
We have prepared a series of strongly fluorescent NO-bis (phenolate) aza-dipyrromethene dyes incorporating boron (aza-BODIPY), aluminum (aza-ALDIPY), gallium (aza-GADIPY), and indium (aza-INDIPY). These compounds were oxidized both chemically and electrochemically to give diradical molecules - with an open-shell singlet ground state and a thermally accessible triplet excited state. The ground state behavior of these diradical molecules was confirmed by a wide array of magnetic spectroscopies, including variable-temperature H NMR, EPR, and SQUID.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Lehrstuhl für Organische Chemie II, Ruhr-Universität Bochum, Universitätsstraße 150, 44801, Bochum, Germany.
We report the first direct observation of the pentafluorophenyl cation in the gas phase via vacuum ultraviolet (VUV) photoionization (PI) of the thermally generated pentafluorophenyl radical. The reactive intermediates and stable reaction products were characterized utilizing photoelectron photoion coincidence (PEPICO) spectroscopy with synchrotron radiation. Electron removal from the pentafluorophenyl radical yields the cation with an adiabatic ionization energy (AIE) of 9.
View Article and Find Full Text PDFJ Chem Phys
July 2025
Department of Chemistry and Biochemistry, Queens College of the City University of New York, 65-30 Kissena Blvd., Queens, New York 11367, USA.
8-oxoguanine (OG) is a prevalent DNA lesion and exhibits a significantly lower oxidation potential than natural nucleic acid components, making the formation of OG•+ radical cation the most efficient hole trap in the one-electron oxidation of DNA. Nitric oxide (•NO) is a precursor to reactive nitrogen species and plays multiple roles in biological activities, including DNA base nitrosation and enhancement of DNA radiosensitivity in radiotherapy. Herein, we report the reaction of •NO with 9-methyl-8-oxoguanine radical cation (9MOG•+), a model compound for OG•+ nucleoside.
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