Search Results

Now showing 1 - 3 of 3
  • Item
    On the Preparation and Spectroelectrochemical Characterization of Certain 2,5-Bis(het)aryl Substituted Thiophenes
    (Weinheim : Wiley-VCH, 2024) Dmitrieva, Evgenia; Barche, Jens; Popov, Alexey A.; Hartmann, Horst
    In this work, a series of novel 2,5-bis(het)aryl and 2,5-bis-thienyl substituted thiophenes have been synthesized and characterized by ultraviolet-visible-near infrared (UV-Vis-NIR) absorption and fluorescence spectroscopy as well as cyclic voltammetry. From the electron paramagnetic resonance (EPR)/UV-Vis-NIR spectroelectrochemical data, information about the optical and magnetic properties of the charged species of these compounds have been provided. The spin distributions in the electrochemically generated radical ions were estimated experimentally and compared with theoretical data.
  • Item
    Capturing Unstable Metallofullerenes
    (Basel : MDPI, 2024) Liu, Fupin; Popov, Alexey A.
    Metallofullerenes are interesting molecules with unique structures and physicochemical properties. After they are formed in the arc-discharge process, they are first buried in the carbon soot, which requires solvent extraction to fish them out, normally followed by HPLC separation. In this minireview, we summarize the main procedures developed to obtain pure metallofullerenes, including well-established extraction with conventional fullerene solvents followed by HPLC (procedure (I) as well as several methods developed for isolation and purification of unstable fullerenes insoluble in conventional fullerene solvents, including chemical modification followed by dissolution (II.1), chemical functionalization during extraction followed by HPLC (II.2), and chemical functionalization of ionic EMFs after redox-extraction followed by HPLC (procedure II.3). The main focus here is on procedure II.3, for which the current status and future perspective are discussed.
  • Item
    Correlation of Work Function and Conformation of C80 Endofullerenes on h-BN/Ni(111)
    (Weinheim : Wiley-VCH, 2024) Stania, Roland; Seitsonen, Ari Paavo; Jung, Hyunjin; Kunhardt, David; Popov, Alexey A.; Muntwiler, Matthias; Greber, Thomas
    Change of conformation or polarization of molecules is an expression of their functionality. If the two correlate, electric fields can change the conformation. In the case of endofullerene single-molecule magnets the conformation is linked to an electric and a magnetic dipole moment, and therefore magnetoelectric effects are envisoned. The interface system of one monolayer Sc2TbN@C80 on hexagonal boron nitride (h-BN) on Ni(111) has been studied. The molecular layer is hexagonally close packedbut incommensurate. With photoemission the polarization and the conformation of the molecules are addressed by the work function and angular intensity distributions. Valence band photoemission (ARPES) shows a temperature-induced energy shift of the C80 molecular orbitals that is parallel to a change in work function of 0.25 eV without charging the molecules. ARPES indicates a modification in molecular conformations between 30 and 300 K. This order–disorder transition involves a polarization change in the interface and is centered at 125 K as observed with high-resolution X-ray photoelectron spectroscopy (XPS). The temperature dependence is described with a thermodynamic model that accounts for disordering with an excitation energy of 74 meV into a high entropy ensemble. All experimental results are supported by density functional theory (DFT).