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1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane
The title compound, C(40)H(56)Cl(2)Si(4), was synthesized by the coupling of 1,1-di-tert-butyl-1,2-dichloro-2,2-diphenyldisilane with lithium. The asymmetric unit contains one half-molecule, which is completed by an inversion centre. In the molecule, the tetrasilane skeleton adopts a perfect ant...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275182/ https://www.ncbi.nlm.nih.gov/pubmed/22347038 http://dx.doi.org/10.1107/S1600536812000669 |
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author | Otsuka, Kyohei Ishida, Shintaro Kyushin, Soichiro |
author_facet | Otsuka, Kyohei Ishida, Shintaro Kyushin, Soichiro |
author_sort | Otsuka, Kyohei |
collection | PubMed |
description | The title compound, C(40)H(56)Cl(2)Si(4), was synthesized by the coupling of 1,1-di-tert-butyl-1,2-dichloro-2,2-diphenyldisilane with lithium. The asymmetric unit contains one half-molecule, which is completed by an inversion centre. In the molecule, the tetrasilane skeleton adopts a perfect anti conformation and the Si—Si bonds [2.4355 (5) and 2.4328 (7) Å] are longer than the standard Si—Si bond length (2.34 Å). The Si—Si—Si angle [116.09 (2)°] is larger than the tetrahedral bond angle (109.5°). These long bond lengths and the wide angle are favorable for reducing the steric hindrance among the tert-butyl and the phenyl groups. The dihedral angle between the phenyl rings in the asymmetric unit is 37.36 (8)°. |
format | Online Article Text |
id | pubmed-3275182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32751822012-02-15 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane Otsuka, Kyohei Ishida, Shintaro Kyushin, Soichiro Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(40)H(56)Cl(2)Si(4), was synthesized by the coupling of 1,1-di-tert-butyl-1,2-dichloro-2,2-diphenyldisilane with lithium. The asymmetric unit contains one half-molecule, which is completed by an inversion centre. In the molecule, the tetrasilane skeleton adopts a perfect anti conformation and the Si—Si bonds [2.4355 (5) and 2.4328 (7) Å] are longer than the standard Si—Si bond length (2.34 Å). The Si—Si—Si angle [116.09 (2)°] is larger than the tetrahedral bond angle (109.5°). These long bond lengths and the wide angle are favorable for reducing the steric hindrance among the tert-butyl and the phenyl groups. The dihedral angle between the phenyl rings in the asymmetric unit is 37.36 (8)°. International Union of Crystallography 2012-01-18 /pmc/articles/PMC3275182/ /pubmed/22347038 http://dx.doi.org/10.1107/S1600536812000669 Text en © Otsuka et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Otsuka, Kyohei Ishida, Shintaro Kyushin, Soichiro 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title | 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title_full | 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title_fullStr | 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title_full_unstemmed | 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title_short | 1,1,4,4-Tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
title_sort | 1,1,4,4-tetra-tert-butyl-1,4-dichloro-2,2,3,3-tetraphenyltetrasilane |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275182/ https://www.ncbi.nlm.nih.gov/pubmed/22347038 http://dx.doi.org/10.1107/S1600536812000669 |
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