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个人简介

since 10/2020 Prodekanin der Fakultät für Chemie und Biochemie since 07/2016 Professorin für Anorganische Chemie (W3), Ruhr-Universität Bochum (D) 27.05.2015 Habilitation, Universität Würzburg (D) 01/12 - 06/16 Unabhängiger Gruppenleiter, Universität Würzburg (D) 2011 Postdoc bei Prof. Dr. H. Braunschweig, Universität Würzburg (D) 2009 - 2010 Postdoc bei Prof. Dr. T. Don Tilley, University of California, Berkeley (USA) 19.06.2009 Dr. rer. nat., TU Dortmund (summa cum laude) bei Prof. Dr. C. Strohmann (D) 2002 - 2007 Diplom (Chemie), Universität Würzburg und Philipps-Universität Marburg (D)

研究领域

involves the application of unique carbanionic compounds in main group element and transition metal chemistry. Thereby, we focus on the development of systems that exhibit versatile functionalities and unusual chemical and electronic properties to allow for new transformations and reactivities. The overall research strategy aims at an advanced understanding of the electronic structure and charge distribution within the prepared systems. For this purpose we are combining experimental and analytical methods with computational studies. The obtained knowledge and understanding allows for a control of stabilities and reactivities, which we use to develope new applications such as in bond activation reactions, the developement of new synthetic strategies and catalytic transformation. Our ongoing research projects involve the use of carbanionic compounds in elementorganic and organometallic chemistry. Thereby, we are focusing on three different compound classes: dianionic compounds (methandiides), carbenoids and ylidic compounds as unique carbon bases.

近期论文

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M. Jörges, F. Krischer, V. H. Gessner Transition metal-free ketene formation from carbon monoxide through isolable ketenyl anions Science, 2022, 378, 1331-1336; doi: 10.1126/science.ade4563 I. Rodstein, L. Kelling, J. Löffler, T. Scherpf, A. Sarbajna, D.M. Andrada and V.H. Gessner Formation of exceptional monomeric YPhos–PdCl2 complexes with high activities in coupling reactions Chem. Sci. 2022,13, 13552-13562. doi: 10.1039/D2SC04523K S. Jäger, P. Meyer, K.-S. Feichtner, S. Henkel, G.W. Schwaab, V.H. Gessner, M. Havenith Reaction of lithium hexamethyldisilazide (LiHMDS) with water at ultracold conditions Phys. Chem. Chem. Phys. 2022, 24, 24089–24094. doi: 10.1039/D2CP03372K J.-A. Zur, M. Schmidt, K.-S. Feichtner, P. Duari, J. Löffler, T. Scherpf, V.H. Gessner From Stable PH-Ylides to α-Carbanionic Phosphines as Ligands for Zwitterionic Catalysts Angew. Chem.Int. Ed. 2022, e202203950. doi: 10.1002/anie.202203950 X.-J. Wei, B. Xue, J. Handelmann, Z. Hu, H. Darmandeh, V.H. Gessner*, L.J. Gooßen*Ylide-Functionalized Diisopropyl Phosphine (prYPhos): A Ligand for Selective Suzuki-Miyaura Couplings of Aryl Chlorides Adv. Synth.Catal. 2022, 364, 3336-3341. doi: 10.1002/adsc.202200321 S. Lapointe, A. Sarbajna, and V.H. Gessner*Ylide-Substituted Phosphines: A Platform of Strong Donor Ligands for Gold Catalysis and Palladium-Catalyzed Coupling Reactions Acc. Chem. Res. 2022, 55, 5, 770–782. doi: 10.1021/acs.accounts.1c00797 P. Neigenfind, D. Knyszek, J. Handelmann and V.H. Gessner*Synthesis of sterically encumbered di- and triarylamines by palladium-catalysed C–N coupling reactions under mild reaction conditions Catal. Sci. Technol., 2022, 12, 3447-3453. doi: 10.1039/D1CY02352G T. Stalder, F. Krischer, H. Steinert, P. Neigenfind, V.H. Gessner*Ylide-stabilized phosphenium cations: Impact of the substitution pattern on the coordination chemistry Chem. Eur. J. 2022, 28, e202104074. doi: 10.1002/chem.202104074 A. Sarbajna, V. H. Gessner* Tritiation gets selective (News and Views) Nature Synthesis, 2022, 1, 16–17. H. Steinert, J. Löffler, V.H. Gessner Single-Site and Cooperative Bond Activation Reactions with Ylide-Functionalized Tetrylenes: A Computational Study Eur. J. Inorg. Chem. 2021, 5004-5013. doi: 10.1002/ejic.202100816 K.-S. Feichtner, L. Scharf, T. Scherpf, B. Mallick, N. Boysen, V.H. Gessner*Tuning Ruthenium Carbene Complexes for Selective P–H activation via Metal-Ligand Cooperation Chem. Eur. J. 2021, 27, 17351-17360. doi: 10.1002/chem.202103151 M. Jörges, A. Kroll, L. Kelling, R. Gauld, B. Mallick, S.M. Huber, V.H. Gessner*Synthesis, Crystal and Electronic Structures of a Thiophosphinoyl- and Amino-Substituted Metallated Ylide Chem. Open, 2021, 10, 1089-1094. doi: 10.1002/open.202100187 V. H. Gessner Coordination Chemistry of Methandiides and Related Ligands. In Comprehensive Coordination Chemistry III; Constable, E. C., Parkin, G., Que Jr, L., Eds., Vol. 1, Elsevier, 2021; pp 667–687. doi: 10.1016/B978-0-08-102688-5.00076-3. J. Löffler, R. M. Gauld, K.-S. Feichtner, I. Rodstein, J.-A. Zur, J. Handelmann, C. Schwarz, V. H. Gessner*Ylide-substituted Phosphines with a Cyclic Ylide-Backbone: Angle Dependence of the Donor Strength Organometallics, 2021, 2888-2900. doi: 10.1021/acs.organomet.1c00349. H. Darmandeh, J. Löffler, N. V. Tzouras, B. Dereli, T. Scherpf, K.-S. Feichtner, S. V. Broeck, K. Van Hecke, M. Saab, C. S. J. Cazin, L. Cavallo, S. P. Nolan*, V. H. Gessner*Au···H-C Hydrogen Bonds as Design Principle in Gold(I) Catalysis Angew. Chem. Int. Ed. 2021, 21014-21024. doi: 10.1002/anie.202108581. J. Handelmann, C.N. Babu, H. Steinert, C. Schwarz, T. Scherpf, A. Kroll and V.H. Gessner*Towards the Rational Design of Ylide-Substituted Phosphines for Gold(I)-Catalysis: From Inactive to ppm-level Catalysis Chem. Sci. 2021, 12, 4329 - 4337. doi: 10.1039/D1SC00105A. Z. Hu, X.-J. Wei, J. Handelmann, A.-K. Seitz, I. Rodstein, V. H. Gessner,* L. J. Gooßen*Coupling of Reformatsky Reagents with Aryl Chlorides enabled by Ylide-Functionalized Phosphine Ligands Angew. Chem. Int. Ed. 2021, 60, 6778–6783. doi: 10.1002/anie.202016048. K. Dilchert, M. Schmidt, A. Großjohann, K.-S. Feichtner, R. E. Mulvey*, V. H. Gessner*Solvation Effects on the Structure and Stability of Alkali Metal Carbenoids Angew. Chem. Int. Ed. 2021, 60, 493-498. doi: 10.1002/anie.202011278 A. Sarbajna, V.S.V.S.N. Swamy and V.H. Gessner*Phosphorus-Ylides: Powerful Substituents for the Stabilization of Reactive Main Group Compounds. Chem. Sci. 2021, 2016-2024. doi: 10.1039/D0SC03278F

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