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Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane
The dehydropolymerisation of phenylsilane is investigated using group 4 metallocene amide complexes as catalysts. The dinuclear zirconocene amide complex Cp(2)Zr(NMe(2))(μ-Me(3)SiC(3)SiMe(3))Zr(NMe(2))Cp(2) (2) (Cp = η(5)-cyclopentadienyl) shows high activity in dehydrocoupling reactions, producing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477068/ https://www.ncbi.nlm.nih.gov/pubmed/36275119 http://dx.doi.org/10.1039/d2ra04955d |
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author | Lindenau, Kevin Spannenberg, Anke Reiß, Fabian Beweries, Torsten |
author_facet | Lindenau, Kevin Spannenberg, Anke Reiß, Fabian Beweries, Torsten |
author_sort | Lindenau, Kevin |
collection | PubMed |
description | The dehydropolymerisation of phenylsilane is investigated using group 4 metallocene amide complexes as catalysts. The dinuclear zirconocene amide complex Cp(2)Zr(NMe(2))(μ-Me(3)SiC(3)SiMe(3))Zr(NMe(2))Cp(2) (2) (Cp = η(5)-cyclopentadienyl) shows high activity in dehydrocoupling reactions, producing polyphenylsilanes with molecular weights ranging from 200 to 3000 g mol(−1) and linear-to-cyclic product ratios of up to 80 : 20. Likewise, different ratios of oligomers and polymers with different tacticities could be described. Ansa-zirconocene amide complexes possessing the ebthi (ebthi = 1,2-ethylene-1,1′-bis(η(5)-tetrahydroindenyl)) ligand systems were prepared and evaluated for catalytic dehydropolymerisation in comparison to the dinuclear catalyst system. |
format | Online Article Text |
id | pubmed-9477068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-94770682022-10-20 Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane Lindenau, Kevin Spannenberg, Anke Reiß, Fabian Beweries, Torsten RSC Adv Chemistry The dehydropolymerisation of phenylsilane is investigated using group 4 metallocene amide complexes as catalysts. The dinuclear zirconocene amide complex Cp(2)Zr(NMe(2))(μ-Me(3)SiC(3)SiMe(3))Zr(NMe(2))Cp(2) (2) (Cp = η(5)-cyclopentadienyl) shows high activity in dehydrocoupling reactions, producing polyphenylsilanes with molecular weights ranging from 200 to 3000 g mol(−1) and linear-to-cyclic product ratios of up to 80 : 20. Likewise, different ratios of oligomers and polymers with different tacticities could be described. Ansa-zirconocene amide complexes possessing the ebthi (ebthi = 1,2-ethylene-1,1′-bis(η(5)-tetrahydroindenyl)) ligand systems were prepared and evaluated for catalytic dehydropolymerisation in comparison to the dinuclear catalyst system. The Royal Society of Chemistry 2022-09-15 /pmc/articles/PMC9477068/ /pubmed/36275119 http://dx.doi.org/10.1039/d2ra04955d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Lindenau, Kevin Spannenberg, Anke Reiß, Fabian Beweries, Torsten Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title | Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title_full | Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title_fullStr | Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title_full_unstemmed | Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title_short | Mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
title_sort | mono- and dinuclear zirconocene(iv) amide complexes for the catalytic dehydropolymerisation of phenylsilane |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477068/ https://www.ncbi.nlm.nih.gov/pubmed/36275119 http://dx.doi.org/10.1039/d2ra04955d |
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