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[1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate
In the title salt, C(12)H(20)NO(+)·CH(3)SO(3) (−), the [1-(1-adamantylamino)ethylidene]oxonium cations and methanesulfonate anions are linked into chains along the a axis via O—H⋯O and N—H⋯O hydrogen bonds. All non-H atoms of the acetamido group are essentially planar, with a maximum deviation of...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969600/ https://www.ncbi.nlm.nih.gov/pubmed/21583164 http://dx.doi.org/10.1107/S1600536809017632 |
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author | Vícha, Robert Nečas, Marek Kozubková, Zuzana Potáček, Milan |
author_facet | Vícha, Robert Nečas, Marek Kozubková, Zuzana Potáček, Milan |
author_sort | Vícha, Robert |
collection | PubMed |
description | In the title salt, C(12)H(20)NO(+)·CH(3)SO(3) (−), the [1-(1-adamantylamino)ethylidene]oxonium cations and methanesulfonate anions are linked into chains along the a axis via O—H⋯O and N—H⋯O hydrogen bonds. All non-H atoms of the acetamido group are essentially planar, with a maximum deviation of 0.0085 (12) Å. In comparison with related structures, the carbonyl C=O bond is slightly elongated [1.249 (2) Å], whereas the amide C—N bond is shortened [1.292 (2) Å]. |
format | Text |
id | pubmed-2969600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29696002010-12-30 [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate Vícha, Robert Nečas, Marek Kozubková, Zuzana Potáček, Milan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title salt, C(12)H(20)NO(+)·CH(3)SO(3) (−), the [1-(1-adamantylamino)ethylidene]oxonium cations and methanesulfonate anions are linked into chains along the a axis via O—H⋯O and N—H⋯O hydrogen bonds. All non-H atoms of the acetamido group are essentially planar, with a maximum deviation of 0.0085 (12) Å. In comparison with related structures, the carbonyl C=O bond is slightly elongated [1.249 (2) Å], whereas the amide C—N bond is shortened [1.292 (2) Å]. International Union of Crystallography 2009-05-20 /pmc/articles/PMC2969600/ /pubmed/21583164 http://dx.doi.org/10.1107/S1600536809017632 Text en © Vícha et al. 2009 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 Vícha, Robert Nečas, Marek Kozubková, Zuzana Potáček, Milan [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title | [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title_full | [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title_fullStr | [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title_full_unstemmed | [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title_short | [1-(1-Adamantylamino)ethylidene]oxonium methanesulfonate |
title_sort | [1-(1-adamantylamino)ethylidene]oxonium methanesulfonate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969600/ https://www.ncbi.nlm.nih.gov/pubmed/21583164 http://dx.doi.org/10.1107/S1600536809017632 |
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