Sterically constrained tricyclic phosphine: Redox behaviour, reductive and oxidative cleavage of P-C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry

Brand A, Schulz S, Hepp A, Weigand J, Uhl W (2021)

In: Chemical science, 12(10), 3460-3474. doi:10.1039/d0sc06155g

Research article (journal) | Peer reviewed | Published

Synthesis of RhIII and IrIII Complexes Bearing Chelating Di-NHC Ligands Obtained from N9-Imidazolium-Substituted Adenine

Osorio Yáñez R, Hepp A, Tan T, Hahn F (2020)

In: Organometallics, 39(2), 344-352. doi:10.1021/acs.organomet.9b00759

Research article (journal) | Peer reviewed | Published

Cooperative activation of azides by an Al/N-based active Lewis pair - Unexpected insertion of nitrogen atoms into C-Si bonds and formation of AlCN3 heterocycles

Uhl W, Martinewski K, Bruchhage J, Hepp A, Layh M, Dielmann F, Mehlmann P (2020)

In: Zeitschrift für Naturforschung B - A Journal of Chemical Sciences, 75(1-2), 63-71. doi:10.1515/znb-2019-0138

Research article (journal) | Peer reviewed | Published

A Geometrically Constrained Tricyclic Phosphine: Coordination, Ring Expansion by Insertion of CO into a P-C Bond, and Lewis Acid Initiated Formation of an Oligocyclic Molecule with a P2C22backbone

In: , -.

| Peer reviewed

Synthesis of IrIIIHydrido Complexes by Oxidative Addition of Halogenated Theophylline and Adenine Derivatives

In: , -.

| Peer reviewed

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Sterically constrained tricyclic phosphine: Redox behaviour, reductive and oxidative cleavage of P-C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry Brand A, Schulz S, Hepp A, Weigand J, Uhl W (2021) In: Chemical science, 12(10), 3460-3474. doi:10.1039/d0sc06155g Research article (journal) \| Peer reviewed \| Published
MCl2Molecules (M = Zn, Cd, Hg) Coordinated by Trifunctional E/P2-Based FLPs (E = Ga, In): Chelating Coordination of the Metal Atoms and Activation of M-Cl Bonds by E-Cl Interactions Uebing M, Hepp A, Uhl W (2020) In: Organometallics, 2020. doi:10.1021/acs.organomet.0c00300 Research article (journal) \| Peer reviewed \| Published
Synthesis of RhIII and IrIII Complexes Bearing Chelating Di-NHC Ligands Obtained from N9-Imidazolium-Substituted Adenine Osorio Yáñez R, Hepp A, Tan T, Hahn F (2020) In: Organometallics, 39(2), 344-352. doi:10.1021/acs.organomet.9b00759 Research article (journal) \| Peer reviewed \| Published
Dihalides of Sterically Constrained Tricyclic Phosphines, Lewis Acidity and Fluoride Affinity, Chloride Abstraction, and a Phosphonium Cation, Dimethylphosphorane Brand A, Hentschel A, Hepp A, Uhl W (2020) In: European Journal of Inorganic Chemistry, 2020(4), 361-369. doi:10.1002/ejic.201901231 Research article (journal) \| Peer reviewed \| Published
Cooperative activation of azides by an Al/N-based active Lewis pair - Unexpected insertion of nitrogen atoms into C-Si bonds and formation of AlCN3 heterocycles Uhl W, Martinewski K, Bruchhage J, Hepp A, Layh M, Dielmann F, Mehlmann P (2020) In: Zeitschrift für Naturforschung B - A Journal of Chemical Sciences, 75(1-2), 63-71. doi:10.1515/znb-2019-0138 Research article (journal) \| Peer reviewed \| Published
Tridentate Ligand with Three Carbanions as Donor Atoms: Formation of Dinuclear, Heptacyclic Complexes of Boron, Aluminum, or Gallium with B-C-B, Al-C-Al, or Ga-C-Ga Three-Center-Two-Electron Bonds In: , -. \| Peer reviewed
A Geometrically Constrained Tricyclic Phosphine: Coordination, Ring Expansion by Insertion of CO into a P-C Bond, and Lewis Acid Initiated Formation of an Oligocyclic Molecule with a P2C22backbone In: , -. \| Peer reviewed
Al/N-based active Lewis pairs: Isocyanate insertion products as efficient nucleophiles employed for the facile generation of highly functional molecules In: , -. \| Peer reviewed
Synthesis of IrIIIHydrido Complexes by Oxidative Addition of Halogenated Theophylline and Adenine Derivatives In: , -. \| Peer reviewed
Hydrosilylation and Hydrogermylation of CO2 and CS2 by Al and Ga Functionalized Silanes and Germanes – Cooperative Reactivity with Formation of Silyl Formates and Disilylacetals In: , -. \| Peer reviewed