• Dr. Dirk Leifert

    Dr. Dirk Leifert
    © Dirk Leifert
    Akademischer Rat, tenured researcher
    Organisch-Chemisches Institut
    Room OC/BC I - 319
    Corrensstraße 36
    48149 Münster
    Tel: +49(0)251 83-33254
    Fax: +49(0)251 83-36523
  • Academic Career & Functions

    since 2019
    Tenured Research Staff (Research, Infrastructure, Administration) in the Studer Research Group, WWU Münster
    Postdoctoral Researcher in the Studer Research Group
    Feodor Lynen Return Fellowship
    Research Focus: Conjugated polymers, oligo- and polyelectrolytes, oxidative cascade reactions and persistent radicals
    Postdoctoral Researcher in the Bazan Research Group
    Feodor Lynen Research Fellowship
    Research Focus: Design, synthesis and characterization of conjugated polymers, oligo- and polyelectrolytes and their doping mechanism
    PhD in Organic Chemistry (Dr. rer. nat.) with Prof. Armido Studer, WWU Münster, on
    "Radical Chain Reactions via Electron Catalysis or Atom Transfer"
    2013 - 2017
    PhD Studies in the Studer Research Group, WWU Münster
    Feb 2013
    Master of Science in Chemistry
    Master thesis: "Cross dehydrogenative couplings"
    2012 - 2013
    ProTalent - WWU Scholarship Programme
    2008 - 2013
    BSc and MSc in Chemistry, WWU Münster
    Abitur, Thomas-Morus-Gymnasium Oelde, North Rhine-Westphalia

  • Publications

    Photoswitchable Conjugated Oligoelectrolytes for Light‐Induced Change of Membrane Morphology,
    D. Leifert, A. S. Moreland, J. Limwongyut, A. A. Mikhailovsky, G. C. Bazan,
    Angew. Chem. Int. Ed. 2020, 59, accepted. [doi:10.1002/ange.202004448]
    Living Bioelectrochemical Composites,
    S. R. McCuskey, Y. Su, D. Leifert, A. S. Moreland, G. C. Bazan,
    Adv. Mater. 2020, 32, 1908178. [doi:10.1002/adma.201908178]
    The Importance of Sulfonate to the Self-doping Mechanism of the Water-Soluble Conjugated Polyelectrolyte PCPDTBT-SO3K,
    D. X. Cao, D. Leifert, V. V. Brus, M. S. Wong, H. Phan, B. Yurash, N. Koch, G. C. Bazan, T.-Q. Nguyen,
    Mater. Chem. Front. 2020, 4, accepted. [doi:10.1039/D0QM00073F]
    The Persistent Radical Effect in Organic Synthesis,
    D. Leifert, A. Studer,
    Angew. Chem. Int. Ed. 2020, 59, 74-108. [doi:10.1002/anie.201903726]
    Towards understanding the doping mechanism of organic semiconductors by Lewis acids,
    B. Yurash, D. X. Cao, V. V. Brus, D. Leifert, M. Wang, A. Dixon, M. Seifrid, A. E. Mansour, D. Lungwitz, T. Liu, P. J. Santiago, K. R. Graham, N. Koch, G. C. Bazan, T.-Q. Nguyen,
    Nat. Mater. 2019, 18, 1327-1334. [doi:10.1038/s41563-019-0479-0]
    Atomic-Level Insight into the Postsynthesis Band Gap Engineering of a Lewis Base Polymer Using Lewis Acid Tris(pentafluorophenyl)borane,
    B. Yurash+, D. Leifert+, G. N. M. Reddy, D. X. Cao, S. Biberger, V. V. Brus, M. Seifrid, P. J. Santiago, A. Köhler, B. F. Chmelka, G. C. Bazan, T.-Q. Nguyen,
    Chem. Mater. 2019, 31, 6715-6725. [doi:10.1021/acs.chemmater.9b01224]
    +These authors contributed equally to this work.
    Electrochemical initiation of electron-catalyzed phenanthridine synthesis by trifluoromethylation of isonitriles,
    M. Lübbesmeyer, D. Leifert, H. Schäfer, A. Studer,
    Chem. Commun. 2018, 54, 2240-2243. [doi:10.1039/C7CC09302K]
    Initiating radical reactions with non-thermal plasmas,
    Y. Gorbanev, D. Leifert, A. Studer, D. O'Connell, V. Chechik,
    Chem. Commun. 2017, 26, 3685-3688. [doi:10.1039/C7CC01157A]
    Iodinated (Perfluoro)alkyl Quinoxalines by Atom Transfer Radical Addition Using ortho‐Diisocyanoarenes as Radical Acceptors,
    D. Leifert, A. Studer,
    Angew. Chem. Int. Ed. 2016, 55, 11660-11663. [doi:10.1002/anie.201606023]
    Radical perfluoroalkylation – easy access to 2-perfluoroalkylindol-3-imines via electron catalysis,
    D. Leifert, D. G. Artiukhin, J. Neugebauer, A. Galstyan, C. A. Strassert, A. Studer,
    Chem. Commun. 2016, 35, 5997-6000. [doi:10.1039/C6CC02284G]
    9-Silafluorenes via base-promoted homolytic aromatic substitution (BHAS) - The electron as a catalyst,
    D. Leifert, A. Studer,
    Org. Lett. 2015, 17, 386-389. [doi:10.1021/ol503574k]
    6-Aroylated phenanthridines via base promoted homolytic aromatic substitution (BHAS),
    D. Leifert, G. C. Daniliuc, A. Studer,
    Org. Lett. 2013, 15, 6286-6289. [doi:10.1021/ol403147v]
    Cross dehydrogenative coupling via base-promoted homolytic aromatic substitution (BHAS): Synthesis of fluorenones and xanthones,
    S. Wertz, D. Leifert, A. Studer,
    Org. Lett. 2013, 15, 928-931. [doi:10.1021/ol4000857]