101 to 110 of 171 Results
Apr 19, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Benedikter, Mathis, 2021, "Data for Silica‐Supported Cationic Tungsten Imido Alkylidene Stabilized by an N‐Heterocyclic Carbene Ligand Boosts Activity and Selectivity in the Metathesis of α‐Olefins", https://doi.org/10.18419/DARUS-1703, DaRUS, V1
All primary data files that were contributed to the publication by the Buchmeiser Research Group can be found here. Data obtained by the Coperet Research Group is not included. Procedures, recation conditions and used analytical equipment is discussed in detail in the experimental section or the supporting information of the paper. NMR Spectra are... |
Mar 23, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Hauser, Philipp Manuel; Musso, Janis; Frey, Wolfgang; Buchmeiser, Michael, 2021, "Publication data for: "Cationic Tungsten Oxo Alkylidene N-Heterocyclic Carbene Complexes via Hydrolysis of Cationic Alkylidyne Progenitors"", https://doi.org/10.18419/DARUS-1772, DaRUS, V1
All primary data files and processed data of the journal article from Buchmeiser group, in which cationic tungsten oxo NHC complexes are synthesized via hydrolysis of cationic alkylidyne NHC complexes. NMR data of all pure compounds and NMR experiments. Gc-MS data of Metathesis reactions and crystal data for all crystal structures. |
Mar 25, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Kesharwani, Manoj Kumar; Elser, Iris; Musso, Janis; Buchmeiser, Michael; Kästner, Johannes, 2021, "Replication data of Buchmeiser group for: Reaction Mechanism of Ring-Closing Metathesis with a Cationic Molybdenum Imido Alkylidene N‑Heterocyclic Carbene Catalyst", https://doi.org/10.18419/DARUS-1714, DaRUS, V1
DFT calculations were carried out to explore all relevant pathways for the ring-closing metathesis (RCM) reaction of a cationic molybdenum imido alkylidene N-heterocyclic carbene (NHC) catalyst with α,ω-dienes.The 1H NMR spectrum of the reaction between [Mo(N-2,6-Me2-C6H3)(CHCMe2Ph)(IMes)(OCH(CF3)2)+ B(ArF)4–] and 1,7-octadiene confirms the absence... |
Mar 5, 2025 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Kundu, Koushani; Buchmeiser, Michael, 2025, "Replication Data for: Origin of Stereoselectivity in Ring Opening Metathesis Polymerization with Cationic Molybdenum Imido Alkylidene CAAC Complexes", https://doi.org/10.18419/DARUS-4791, DaRUS, V1
This dataset includes the NMR (1H, 19F and 13C) of the novel catalysts used in this article, the single crystal X-ray structure of a catalyst, and the proton NMR of the polymers. |
Nov 26, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Ziegler, Felix, 2021, "Data for: "Olefin Ring-closing Metathesis under Spatial Confinement and Continuous Flow"", https://doi.org/10.18419/DARUS-1690, DaRUS, V1
The use of a 2nd-generation Hoveyda-Grubbs-type catalyst immobilized inside mesoporous silica for the application in selective macro(mono)cyclization (MMC) of an alpha,omega-diene under spatially confined and continuous-flow conditions. Data you will find: NMR-Data for the determination of conversion and selectivity of the macrocyclization. MALDI r... |
Nov 15, 2023 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Panyam, Pradeep Kumar Reddy; Buchmeiser, Michael, 2023, "Replication Data for: Effect of liquid confinement on regioselectivity in the hydrosilylation of alkynes with cationic Rh(i) N-heterocyclic carbene catalysts", https://doi.org/10.18419/DARUS-3741, DaRUS, V1
All primary data files related to the publication. Procedures, reaction conditions and used analytical equipment is discussed in detail in the experimental section or the supporting information of the paper. Novel complexes were examined via nuclear magnetic resonance (NMR) spectroscopy and the spectra can be found in NMR folder. The NMR folder als... |
Apr 9, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Elser, Iris; Groos, Jonas; Hauser, Philipp Manuel; van der Ende, Melita; Koy, Maximilian, 2021, "Publication data for: "Molybdenum and Tungsten Alkylidyne Complexes Containing Mono-, Bi-, and Tridentate N-Heterocyclic Carbenes" - data from Buchmeiser group", https://doi.org/10.18419/DARUS-1689, DaRUS, V1
All primary data files and processed data of the journal article from Buchmeiser group. NMR data is in the folder NMR divided in NMR experiments and pure compounds which consists of the NMR spectra of pure compounds.The TONs in table 2 were determined by GC-MS. GC-MS data is in the GC-MS folder and organized by complexes. |
Oct 24, 2023 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Musso, Janis; Gramm, Vincent; Stein, Sarjano; Frey, Wolfgang; Buchmeiser, Michael, 2023, "Replication data of the Buchmeiser group for: "Molybdenum Alkylidyne Silyloxy N-Heterocyclic Carbene Complexes - Highly Active Alkyne Metathesis Catalysts that can be Handled in Air"", https://doi.org/10.18419/DARUS-3267, DaRUS, V1
All primary data files of measurements and processed data of the journal article mentioned under related publications from the Buchmeiser group can be found here. The data consist of: *Processed (mestrenova) and unprocessed (fid-files) NMR spectra of novel compunds *NMR spectra for the mechanistic studies *NMR spectra of the air-stability tests |
Nov 30, 2021 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Ziegler, Felix; Benedikter, Mathis; Wang, Dongren, 2021, "Replication data of Buchmeiser group for: "Confinement Effects for Efficient Macrocyclization Reactions with supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes"", https://doi.org/10.18419/DARUS-2248, DaRUS, V1
All primary data files of measurements and processed data of the journal article mentioned under related publications from Buchmeiser group can be found here. The data is structured according to figures and schemes in the research article and contains the following data types: qps, txt, fid, mnova |
Dec 13, 2024 - SFB 1333 A1+B2 - Buchmeiser group, IPOC-MSF
Nandeshwar, Muneshwar; Weisser, Kilian; Buchmeiser, Michael; Ziegler, Felix, 2024, "Replication Data for: "The Role of Spacer Length in Macrocyclization Reactions Under Confinement"", https://doi.org/10.18419/DARUS-4646, DaRUS, V1
All primary data files associated with this publication, experimental procedures, reaction conditions, and used analytical equipment can be found in detail in the experimental section or the paper's supporting information. Synthesized complexes (Mo1-Mo7) and macrocyclization were characterized via nuclear magnetic resonance (NMR) spectroscopy; the... |