Lehrstuhl für Organische Chemie I

Address:
Nikolaus-Fiebiger-Str. 10
91058 Erlangen



Subordinate Organisational Units

Professur für Organische Chemie
Professur für Organische Chemie


Publications (Download BibTeX)

Go to first page Go to previous page 1 of 10 Go to next page Go to last page

Papadopoulos, I., Zirzlmeier, J., Hetzer, C., Bae, Y.J., Krzyaniak, M.D., Wasielewski, M.R.,... Guldi, D.M. (2019). Varying the Interpentacene Electronic Coupling to Tune Singlet Fission. Journal of the American Chemical Society, 141(15), 6191-6203. https://dx.doi.org/10.1021/jacs.8b09510
Basel, B., Hetzer, C., Zirzlmeier, J., Thiel, D., Guldi, R., Hampel, F.,... Tykwinski, R.R. (2019). Davydov splitting and singlet fission in excitonically coupled pentacene dimers. Chemical Science, 10(13), 3854-3863. https://dx.doi.org/10.1039/c9sc00384c
Marshall, J.L., Arslan, F., Januszewski, J., Ferguson, M.J., & Tykwinski, R.R. (2019). A Tetraethynyl[5]cumulene. Helvetica Chimica Acta, 102(3). https://dx.doi.org/10.1002/hlca.201900001
Daum, S., Toms, J., Reshetnikov, V., Özkan, H., Hampel, F., Maschauer, S.,... Mokhir, A. (2019). Identification of Boronic Acid Derivatives as an Active Form of N-Alkylaminoferrocene-Based Anticancer Prodrugs and Their Radiolabeling with 18F. Bioconjugate Chemistry, 30(4), 1077-1086. https://dx.doi.org/10.1021/acs.bioconjchem.9b00019
Spisak, S.N., Bühringer, M., Wei, Z., Zhou, Z., Tykwinski, R., & Petrukhina, M.A. (2019). Structural and Electronic Effects of Stepwise Reduction of a Tetraaryl[3]Cumulene. Angewandte Chemie-International Edition, 58(7), 2023-2028. https://dx.doi.org/10.1002/anie.201812283
Akhmetov, V., Feofanov, M., Ioutsi, V., Hampel, F., & Amsharov, K. (2019). Unusual Fusion of -Fluorinated Benzophenones under McMurry Reaction Conditions. Chemistry - A European Journal, 25(8), 1910-1913. https://dx.doi.org/10.1002/chem.201805290
Casillas Pacheco, R., Adam, M., Brana Coto, P., Waterloo, A., Zirzlmeier, J., Reddy, S.R.,... Guldi, D.M. (2019). Intermolecular Singlet Fission in Unsymmetrical Derivatives of Pentacene in Solution. Advanced Energy Materials, 9(2). https://dx.doi.org/10.1002/aenm.201802221
Capci Karagöz, A., Leidenberger, M., Hahn, F., Friedrich, O., Hampel, F., Marschall, M.,... Tsogoeva, S. (2019). Synthesis of new betulinic acid/betulin-derived dimers and hybrids with potent antimalarial and antiviral activities. Bioorganic & Medicinal Chemistry, 27(1), 110-115. https://dx.doi.org/10.1016/j.bmc.2018.11.018
Maier, S., Ammon, M., Meyer, B., Kivala, M., Steiner, C., Yang, Z.,... Ammon, M. (2018). Binary supramolecular networks of bridged triphenylamines with different substituents and identical scaffolds. Chemical Communications, 54(82), 11554-11557. https://dx.doi.org/10.1039/c8cc04410d
Basel, B., Zirzlmeier, J., Hetzer, C., Seelam, R.R., Phelan, B.T., Krzyaniak, M.D.,... Guldi, D.M. (2018). Evidence for Charge-Transfer Mediation in the Primary Events of Singlet Fission in a Weakly Coupled Pentacene Dimer. Chem, 4(5), 1092-1111. https://dx.doi.org/10.1016/j.chempr.2018.04.006
Wu, Y., Klein, V., Killian, M., Behling, C., Chea, S., Tsogoeva, S., & Bachmann, J. (2018). Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity. ACS Omega, 3(3), 2602-2608. https://dx.doi.org/10.1021/acsomega.7b01982
Fröhlich, T., Hahn, F., Belmudes, L., Leidenberger, M., Friedrich, O., Kappes, B.,... Tsogoeva, S. (2018). Synthesis of Artemisinin-Derived Dimers, Trimers and Dendrimers: Investigation of Their Antimalarial and Antiviral Activities Including Putative Mechanisms of Action. Chemistry - A European Journal, 24(32), 8103-8113. https://dx.doi.org/10.1002/chem.201800729
Bühringer, M., Padberg, K., Phleps, D., Maid, H., Placht, C., Neiß, C.,... Tykwinski, R. (2018). Double bonds? Studies on the barrier to rotation about the cumulenic C=C bonds of tetraaryl[n]cumulenes (n=3,5,7,9). Angewandte Chemie-International Edition, 57, 8321-8325. https://dx.doi.org/10.1002/anie.201802137
Heller, B., Kolbeck, C., Niedermaier, I., Dommer, S., Schatz, J., Hunt, P.,... Steinrück, H.-P. (2018). Surface Enrichment in Equimolar Mixtures of Non-Functionalized and Functionalized Imidazolium-Based Ionic Liquids. Chemphyschem, 19(14), 1733-1745. https://dx.doi.org/10.1002/cphc.201800216
Kunzmann, A., Gruber, M., Casillas Pacheco, R., Zirzlmeier, J., Stanzel, M., Peukert, W.,... Guldi, D.M. (2018). Singlet Fission for Photovoltaics with 130 % Injection Efficiency. Angewandte Chemie International Edition, 57(33), 10742-10747. https://dx.doi.org/10.1002/anie.201801041
Yang, Z., Gebhardt, J., Schaub, T.A., Sander, T., Schönamsgruber, J., Soni, H.,... Maier, S. (2018). Two-dimensional delocalized states in organometallic bis-acetylide networks on Ag(111). Nanoscale, 10, 3769-3776.
Capci Karagöz, A., Reiter, C., Seo, E.-J., Gruber, L., Hahn, F., Leidenberger, M.,... Tsogoeva, S. (2018). Access to new highly potent antileukemia, antiviral and antimalarial agents via hybridization of natural products (homo)egonol, thymoquinone and artemisinin. Bioorganic & Medicinal Chemistry, 26(12), 3610-3618. https://dx.doi.org/10.1016/j.bmc.2018.05.041
Hahn, F., Fröhlich, T., Frank, T., Bertzbach, L.D., Kohrt, S., Kaufer, B.B.,... Marschall, M. (2018). Artesunate-derived monomeric, dimeric and trimeric experimental drugs - Their unique mechanistic basis and pronounced antiherpesviral activity. Antiviral Research, 152, 104-110. https://dx.doi.org/10.1016/j.antiviral.2018.02.013
Gruber, M., Padberg, K., Min, J., Waterloo, A., Hampel, F., Maid, H.,... Tykwinski, R. (2017). Acenequinocumulenes: Lateral and vertical π-extended analogs of tetracyanoquinodimethane (TCNQ). Chemistry - A European Journal, 23(70), 17829-17835. https://dx.doi.org/10.1002/chem.201704314
Bock, C., Gangajji, P., Bönisch, S., Bauer, W., Hutterer, C., Leidenberger, M.,... Tsogoeva, S. (2017). Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products. ChemistryOpen, 6(3), 364-374. https://dx.doi.org/10.1002/open.201700005

Last updated on 2019-24-04 at 10:21