Data for: "Cationic Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts" (doi:10.18419/darus-1698)

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Data for: "Cationic Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts"

doi:10.18419/darus-1698

DaRUS

2021-04-22

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Benedikter, Mathis, 2021, "Data for: "Cationic Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts"", https://doi.org/10.18419/darus-1698, DaRUS, V1

Data for: "Cationic Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts"

doi:10.18419/darus-1698

Benedikter, Mathis (Universität Stuttgart)

358283783 - SFB 1333

DaRUS

Buchmeiser, Michael

Benedikter, Mathis

2021-03-11

https://doi.org/10.18419/darus-1698

Chemistry, metal complex, metathesis, catalysis, transition metal, molybdenum, tungsten

inorganic chemistry

All primary data files related to the publication. Procedures, recation conditions and used analytical equipment is discussed in detail in the experimental section or the supporting information of the paper. Productivities in olefin metathesis reactions were examined via gas-chromatography / mass spectrometry (GC-MS) analysis and can be found in the GC-MS folder. Furthermore, the GC-MS folder contains an Excel-file in which the names of the data files are listed and assigned to table entries in the publication. Novel complexes were examined via nuclear magnetic resonance (NMR) spectroscopy and the spectra can be found in NMR folder. The NMR folder also contains NMR experiments mentioned in the paper and shown in the Supplementary Information. NMR Spectra are named according to the numbering in the publication. All crystal data mentioned in the paper can be found in the related datasets. Size exclusion chromatography (SEC) data are provided as text-files and can be plotted with software such as MS Excel.

NMR spectra were processed with MestreNova. GC-MS data was processed with Agilent MassHunter.

CCDC 2023958 (W-13, <a href="https://doi.org/10.5517/ccdc.csd.cc25y2z6">DOI: 10.5517/ccdc.csd.cc25y2z6</a>)

CCDC 2023959 (W-14, <a href="https://doi.org/10.5517/ccdc.csd.cc25y308">DOI: 10.5517/ccdc.csd.cc25y308</a>)

M. J. Benedikter, J. V. Musso, W. Frey, R. Schowner, M. R. Buchmeiser, Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts. Angew. Chem. Int. Ed. 2021, 60, 1374.

10.1002/anie.202011666

M. J. Benedikter, J. V. Musso, W. Frey, R. Schowner, M. R. Buchmeiser, Group VI Metal Imido Alkylidene N‐Heterocyclic Carbene Nitrile Complexes: Bench‐Stable, Functional‐Group‐Tolerant Olefin Metathesis Catalysts. Angew. Chem. Int. Ed. 2021, 60, 1374.

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kinetics.zip

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productivities.zip

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sample names.xlsx

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air-stability experiments.zip

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NMR experiments.zip

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polymerizations.zip

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pure compounds.zip

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poly(M1-Mo03).TXT

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column 1: intensity of the RI signal [a.u.] column 2: time [min]

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poly(M1-Mo03-MeCN).TXT

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column 1: intensity of the RI signal [a.u.]; column 2: time [min]

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poly(M1-Mo04).TXT

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column 1: intensity of the RI signal [a.u.] column 2: time [min]

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poly(M1-Mo04-MeCN).TXT

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column 1: intensity of the RI signal [a.u.] column 2: time [min]

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