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Replication Data for: Origin of Stereoselectivity in Ring Opening Metathesis Polymerization with Cationic Molybdenum Imido Alkylidene CAAC Complexes

, und . Dataset, (2025)Related to: Koushani Kundu, Severin Haid, Moritz R. Schäfer, Wolfgang Frey, Johannes Kästner, Michael R. Buchmeiser; Origin of Stereoselectivity in Ring Opening Metathesis Polymerization with Cationic Molybdenum Imido Alkylidene CAAC Complexes. ACS Catal. 2025, 15, 2, 738-747. doi: 10.1021/acscatal.4c07610.
DOI: 10.18419/darus-4791

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Univ. -Prof. Dr. Michael Buchmeiser University of Stuttgart

Michael Kübler University of Stuttgart

Michael Kölle University of Stuttgart

Dr. Michael Böhm University of Stuttgart

Michael Böhm

 

Weitere Publikationen von Autoren mit dem selben Namen

Data for "Betainic and ionic tungsten (VI) imido alkylidene N-heterocyclic olefin complexes", , , und . Dataset, (2023)Related to: Michael R. Buchmeiser, Dominik Imbrich, Dongren Wang, Stefan Naumann. Betainic and ionic tungsten (VI) imido alkylidene N-heterocyclic olefin complexes. J. Organomet. Chem. 2023, 991, 122674. doi: 10.1016/j.jorganchem.2023.122674.Chemistry and Properties of Carbon Fiber Feedstocks from Bitumen Asphaltenes, , , , , , , , , und . Energy & fuels, 37 (7): 5341-5360 (2023)Replication data of the Buchmeiser Group for "Macrocyclization of Dienes Under Confinement With Cationic Tungsten Imido/Oxo Alkylidene N-Heterocyclic Carbene Complexes", , , , , , und . Dataset, (2023)Related to: Ziegler, F., Bruckner, J. R., Nowakowski, M., Bauer, M., Probst, P., Atwi, B., Buchmeiser, M. R., Macrocyclization of Dienes under Confinement with Cationic Tungsten Imido/Oxo Alkylidene N-Heterocyclic Carbene Complexes. ChemCatChem 2023, e202300871. doi: 10.1002/cctc.202300871.Tungsten Oxo and Tungsten Imido Alkylidene N-Heterocyclic Carbene Complexes for the Visible-Light-Induced Ring-Opening Metathesis Polymerization of Dicyclopentadiene, , , , und . Macromolecules, 56 (7): 2878-2888 (2023)Replication Data for: Effect of liquid confinement on regioselectivity in the hydrosilylation of alkynes with cationic Rh(i) N-heterocyclic carbene catalysts, und . Dataset, (2023)Related to: Pradeep K. R. Panyam and Michael R. Buchmeiser. Effect of liquid confinement on regioselectivity in the hydrosilylation of alkynes with cationic Rh(I) N-heterocyclic carbene catalysts. Faraday Discuss., 2023, 244, 39-50. doi: 10.1039/d2fd00152g.Replication Data for: Hydrosilylation of Alkynes Under Continuous Flow Using Polyurethane-Based Monolithic Supports with Tailored Mesoporosity, , , , , , und . Dataset, (2023)Related to: Hande Acikalin, Pradeep K. R. Panyam, Abdul Wasif Shaikh, Dongren Wang, Shravan R. Kousik, Petia Atanasova, Michael R. Buchmeiser. Hydrosilylation of Alkynes Under Continuous Flow Using Polyurethane-Based Monolithic Supports with Tailored Mesoporosity. Macromol. Chem. Phys. 2023, 224, 2200234. doi: 10.1002/macp.202200234.Synthesis of Linear Poly(oxazolidin-2-one)s by Cooperative Catalysis Based on N-Heterocyclic Carbenes and Simple Lewis Acids, , , , , , , , und . Macromolecules, 52 (2): 487-494 (2019)Vanadium(v) arylimido alkylidene N-heterocyclic carbene complexes containing fluorinated alkoxide or halogenated phenoxide ligands for the syndiospecific ROMP of cyclic olefins, , , , , und . New journal of chemistry, 48 (34): 14865-14872 (2024)Feed injection in liquid chromatography: Reducing the effect of large-volume injections from purely organic diluents in reversed-phase liquid chromatography, , , , , , , , und . Journal of chromatography. A, (2024)Supplementary material for "Influence of Ionic Liquid Film Thickness and Flow Rate on Macrocyclization Efficiency and Selectivity in Supported Ionic Liquid-Liquid Phase Catalysis", , , , , , und . Dataset, (2025)Related to: Högler, Marc; Kobayashi, Takeshi; Kraus, Hamzeh; Atwi, Boshra; Buchmeiser, Michael R.; Fyta, Maria, Hansen, Niels (2025): Influence of Ionic Liquid Film Thickness and Flow Rate on Macrocyclization Efficiency and Selectivity in Supported Ionic Liquid-Liquid Phase Catalysis. In: Chemistry - A European Journal, 31, e202403237. doi: 10.1002/chem.202403237.