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Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation
Hydrosilylation with octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) (1) has provided hundreds of molecular and macromolecular systems so far, making this method the most popular in the synthesis of siloxane-based, nanometric, cubic, and reactive building blocks. However, there are no reports on its sel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471723/ https://www.ncbi.nlm.nih.gov/pubmed/37653063 http://dx.doi.org/10.1038/s41598-023-41461-2 |
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author | Stefanowska, Kinga Nagórny, Jakub Szyling, Jakub Franczyk, Adrian |
author_facet | Stefanowska, Kinga Nagórny, Jakub Szyling, Jakub Franczyk, Adrian |
author_sort | Stefanowska, Kinga |
collection | PubMed |
description | Hydrosilylation with octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) (1) has provided hundreds of molecular and macromolecular systems so far, making this method the most popular in the synthesis of siloxane-based, nanometric, cubic, and reactive building blocks. However, there are no reports on its selective reaction with 1,3-diynes, which allows for the formation of new products with unique properties. Therefore, herein we present an efficient protocol for monohydrosilylation of symmetrically and non-symmetrically 1,4-disubstituted buta-1,3-diynes with 1. The compounds obtained bear double and triple bonds and other functionalities (e.g., Br, F, OH, SiR(3)), making them highly desirable, giant building blocks in organic synthesis and material chemistry. These compounds were fully characterized by (1)H, (13)C, (29)Si, 1D NOE, (1)H–(13)C HSQC NMR, FT–IR, and MALDI TOF MS, EA, UV–Vis, and TGA analysis. The TGA proved their high thermal stability up to 427 ℃ (T(d)(10%)) for compound 3j. |
format | Online Article Text |
id | pubmed-10471723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104717232023-09-02 Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation Stefanowska, Kinga Nagórny, Jakub Szyling, Jakub Franczyk, Adrian Sci Rep Article Hydrosilylation with octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) (1) has provided hundreds of molecular and macromolecular systems so far, making this method the most popular in the synthesis of siloxane-based, nanometric, cubic, and reactive building blocks. However, there are no reports on its selective reaction with 1,3-diynes, which allows for the formation of new products with unique properties. Therefore, herein we present an efficient protocol for monohydrosilylation of symmetrically and non-symmetrically 1,4-disubstituted buta-1,3-diynes with 1. The compounds obtained bear double and triple bonds and other functionalities (e.g., Br, F, OH, SiR(3)), making them highly desirable, giant building blocks in organic synthesis and material chemistry. These compounds were fully characterized by (1)H, (13)C, (29)Si, 1D NOE, (1)H–(13)C HSQC NMR, FT–IR, and MALDI TOF MS, EA, UV–Vis, and TGA analysis. The TGA proved their high thermal stability up to 427 ℃ (T(d)(10%)) for compound 3j. Nature Publishing Group UK 2023-08-31 /pmc/articles/PMC10471723/ /pubmed/37653063 http://dx.doi.org/10.1038/s41598-023-41461-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Stefanowska, Kinga Nagórny, Jakub Szyling, Jakub Franczyk, Adrian Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title | Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title_full | Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title_fullStr | Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title_full_unstemmed | Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title_short | Functionalization of octaspherosilicate (HSiMe(2)O)(8)Si(8)O(12) with buta-1,3-diynes by hydrosilylation |
title_sort | functionalization of octaspherosilicate (hsime(2)o)(8)si(8)o(12) with buta-1,3-diynes by hydrosilylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471723/ https://www.ncbi.nlm.nih.gov/pubmed/37653063 http://dx.doi.org/10.1038/s41598-023-41461-2 |
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