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Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts
A new type of molybdenum alkylidyne catalysts for alkyne metathesis is described, which is distinguished by an unconventional podand topology. These structurally well‐defined complexes are easy to make on scale and proved to be tolerant toward numerous functional groups; even certain protic substitu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856820/ https://www.ncbi.nlm.nih.gov/pubmed/31449713 http://dx.doi.org/10.1002/anie.201908571 |
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author | Hillenbrand, Julius Leutzsch, Markus Fürstner, Alois |
author_facet | Hillenbrand, Julius Leutzsch, Markus Fürstner, Alois |
author_sort | Hillenbrand, Julius |
collection | PubMed |
description | A new type of molybdenum alkylidyne catalysts for alkyne metathesis is described, which is distinguished by an unconventional podand topology. These structurally well‐defined complexes are easy to make on scale and proved to be tolerant toward numerous functional groups; even certain protic substituents were found to be compatible. The new catalysts were characterized by X‐ray crystallography and by spectroscopic means, including (95)Mo NMR. |
format | Online Article Text |
id | pubmed-6856820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68568202019-11-21 Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts Hillenbrand, Julius Leutzsch, Markus Fürstner, Alois Angew Chem Int Ed Engl Communications A new type of molybdenum alkylidyne catalysts for alkyne metathesis is described, which is distinguished by an unconventional podand topology. These structurally well‐defined complexes are easy to make on scale and proved to be tolerant toward numerous functional groups; even certain protic substituents were found to be compatible. The new catalysts were characterized by X‐ray crystallography and by spectroscopic means, including (95)Mo NMR. John Wiley and Sons Inc. 2019-09-17 2019-10-28 /pmc/articles/PMC6856820/ /pubmed/31449713 http://dx.doi.org/10.1002/anie.201908571 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Hillenbrand, Julius Leutzsch, Markus Fürstner, Alois Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title | Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title_full | Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title_fullStr | Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title_full_unstemmed | Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title_short | Molybdenum Alkylidyne Complexes with Tripodal Silanolate Ligands: The Next Generation of Alkyne Metathesis Catalysts |
title_sort | molybdenum alkylidyne complexes with tripodal silanolate ligands: the next generation of alkyne metathesis catalysts |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856820/ https://www.ncbi.nlm.nih.gov/pubmed/31449713 http://dx.doi.org/10.1002/anie.201908571 |
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