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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...

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Detalles Bibliográficos
Autores principales: Ioannou, Savvas, Moushi, Eleni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
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.
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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
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