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2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate
In the title compound, C(27)H(27)N(3)O(3)S(3)·CH(4)O, the dihedral angles formed by the mesitylene ring with the three oxopyridyl rings are 89.6 (1), 75.5 (1) and 80.69 (1)°, indicating that all three are nearly perpendicular to the mesitylene ring. Intramolecular C—H⋯S hydrogen bonds generate S(6)...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961605/ https://www.ncbi.nlm.nih.gov/pubmed/21202559 http://dx.doi.org/10.1107/S1600536808013081 |
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author | Ravindran Durai Nayagam, B. Jebas, Samuel Robinson Ravi Samuelraj, C. Schollmeyer, Dieter |
author_facet | Ravindran Durai Nayagam, B. Jebas, Samuel Robinson Ravi Samuelraj, C. Schollmeyer, Dieter |
author_sort | Ravindran Durai Nayagam, B. |
collection | PubMed |
description | In the title compound, C(27)H(27)N(3)O(3)S(3)·CH(4)O, the dihedral angles formed by the mesitylene ring with the three oxopyridyl rings are 89.6 (1), 75.5 (1) and 80.69 (1)°, indicating that all three are nearly perpendicular to the mesitylene ring. Intramolecular C—H⋯S hydrogen bonds generate S(6) ring motifs. The crystal structure is stabilized by intramolecular C—H⋯S and intermolecular C—H⋯O hydrogen bonds and weak C—H⋯π interactions. |
format | Text |
id | pubmed-2961605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29616052010-12-30 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate Ravindran Durai Nayagam, B. Jebas, Samuel Robinson Ravi Samuelraj, C. Schollmeyer, Dieter Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(27)N(3)O(3)S(3)·CH(4)O, the dihedral angles formed by the mesitylene ring with the three oxopyridyl rings are 89.6 (1), 75.5 (1) and 80.69 (1)°, indicating that all three are nearly perpendicular to the mesitylene ring. Intramolecular C—H⋯S hydrogen bonds generate S(6) ring motifs. The crystal structure is stabilized by intramolecular C—H⋯S and intermolecular C—H⋯O hydrogen bonds and weak C—H⋯π interactions. International Union of Crystallography 2008-05-10 /pmc/articles/PMC2961605/ /pubmed/21202559 http://dx.doi.org/10.1107/S1600536808013081 Text en © Ravindran Durai Nayagam et al. 2008 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 Ravindran Durai Nayagam, B. Jebas, Samuel Robinson Ravi Samuelraj, C. Schollmeyer, Dieter 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title | 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title_full | 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title_fullStr | 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title_full_unstemmed | 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title_short | 2,4,6-Tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
title_sort | 2,4,6-tris(1-oxo-2-pyridylsulfanylmethyl)mesitylene methanol solvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961605/ https://www.ncbi.nlm.nih.gov/pubmed/21202559 http://dx.doi.org/10.1107/S1600536808013081 |
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