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Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes
[Image: see text] Tetramethyldisiloxa[3]metallocenophanes of the heavy group 14 elements germanium, 2a, tin, 2b, and lead, 2c, (tetrelocenophanes) have been synthesized by the reaction of dilithiated ligand, 1, with the corresponding element(II) chloride. The plumbocenophane, 2c, forms one-dimension...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844111/ https://www.ncbi.nlm.nih.gov/pubmed/31720537 http://dx.doi.org/10.1021/acsomega.9b02605 |
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author | Wirtz, Lisa Jourdain, Matthias Huch, Volker Zimmer, Michael Schäfer, André |
author_facet | Wirtz, Lisa Jourdain, Matthias Huch, Volker Zimmer, Michael Schäfer, André |
author_sort | Wirtz, Lisa |
collection | PubMed |
description | [Image: see text] Tetramethyldisiloxa[3]metallocenophanes of the heavy group 14 elements germanium, 2a, tin, 2b, and lead, 2c, (tetrelocenophanes) have been synthesized by the reaction of dilithiated ligand, 1, with the corresponding element(II) chloride. The plumbocenophane, 2c, forms one-dimensional coordination polymers in the solid state, while the germanocenophane, 2a, and the stannocenophane, 2b, are monomeric. Furthermore, the reactivity of the stannocenophane, 2b, and the plumbocenophane, 2c, toward N-heterocyclic carbenes was explored. Although the coordination of carbene is reversible in solution at room temperature, the corresponding carbene complexes, 3a,b, could be structurally characterized, illustrating the Lewis acidity of the central atom in these metallocenophanes. |
format | Online Article Text |
id | pubmed-6844111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68441112019-11-12 Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes Wirtz, Lisa Jourdain, Matthias Huch, Volker Zimmer, Michael Schäfer, André ACS Omega [Image: see text] Tetramethyldisiloxa[3]metallocenophanes of the heavy group 14 elements germanium, 2a, tin, 2b, and lead, 2c, (tetrelocenophanes) have been synthesized by the reaction of dilithiated ligand, 1, with the corresponding element(II) chloride. The plumbocenophane, 2c, forms one-dimensional coordination polymers in the solid state, while the germanocenophane, 2a, and the stannocenophane, 2b, are monomeric. Furthermore, the reactivity of the stannocenophane, 2b, and the plumbocenophane, 2c, toward N-heterocyclic carbenes was explored. Although the coordination of carbene is reversible in solution at room temperature, the corresponding carbene complexes, 3a,b, could be structurally characterized, illustrating the Lewis acidity of the central atom in these metallocenophanes. American Chemical Society 2019-10-21 /pmc/articles/PMC6844111/ /pubmed/31720537 http://dx.doi.org/10.1021/acsomega.9b02605 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wirtz, Lisa Jourdain, Matthias Huch, Volker Zimmer, Michael Schäfer, André Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title | Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title_full | Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title_fullStr | Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title_full_unstemmed | Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title_short | Synthesis, Structure, and Reactivity of Disiloxa[3]tetrelocenophanes |
title_sort | synthesis, structure, and reactivity of disiloxa[3]tetrelocenophanes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844111/ https://www.ncbi.nlm.nih.gov/pubmed/31720537 http://dx.doi.org/10.1021/acsomega.9b02605 |
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