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Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene
The title compound, C(18)H(24), was the main product of thermolysis of noradamantene dimer (heptacyclo[9.3.1.1(2,6).1(4,8).1(9,13).0(1,9).0(2,8)]octadecane). The crystal structure was determined to prove that the thermolysis product of noradamantene dimer is favored by stretch release due to rin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393958/ https://www.ncbi.nlm.nih.gov/pubmed/22798823 http://dx.doi.org/10.1107/S1600536812026785 |
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author | Ioannou, Savvas Moushi, Eleni |
author_facet | Ioannou, Savvas Moushi, Eleni |
author_sort | Ioannou, Savvas |
collection | PubMed |
description | The title compound, C(18)H(24), was the main product of thermolysis of noradamantene dimer (heptacyclo[9.3.1.1(2,6).1(4,8).1(9,13).0(1,9).0(2,8)]octadecane). The crystal structure was determined to prove that the thermolysis product of noradamantene dimer is favored by stretch release due to ring opening of the four-membered ring. The bond length of the quaternary C atoms of the starting material was calculated as 1.6 Å, enlarged in comparison to other single bonds. After the rearrangement, the stretch release of the above carbons leads to an increase of the distance between them (2.824 Å) with respect to the crystallographic data. |
format | Online Article Text |
id | pubmed-3393958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33939582012-07-13 Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene Ioannou, Savvas Moushi, Eleni Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(24), was the main product of thermolysis of noradamantene dimer (heptacyclo[9.3.1.1(2,6).1(4,8).1(9,13).0(1,9).0(2,8)]octadecane). The crystal structure was determined to prove that the thermolysis product of noradamantene dimer is favored by stretch release due to ring opening of the four-membered ring. The bond length of the quaternary C atoms of the starting material was calculated as 1.6 Å, enlarged in comparison to other single bonds. After the rearrangement, the stretch release of the above carbons leads to an increase of the distance between them (2.824 Å) with respect to the crystallographic data. International Union of Crystallography 2012-06-20 /pmc/articles/PMC3393958/ /pubmed/22798823 http://dx.doi.org/10.1107/S1600536812026785 Text en © Ioannou and Moushi 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 Ioannou, Savvas Moushi, Eleni Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title | Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title_full | Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title_fullStr | Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title_full_unstemmed | Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title_short | Pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
title_sort | pentacyclo[9.3.1.1(2,6).1(4,8).1(9,13)]octadeca-1(2),8(9)-diene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393958/ https://www.ncbi.nlm.nih.gov/pubmed/22798823 http://dx.doi.org/10.1107/S1600536812026785 |
work_keys_str_mv | AT ioannousavvas pentacyclo9311261481913octadeca1289diene AT moushieleni pentacyclo9311261481913octadeca1289diene |