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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...

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Autores principales: Wirtz, Lisa, Jourdain, Matthias, Huch, Volker, Zimmer, Michael, Schäfer, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
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.
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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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