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2-Hydroxybenzyl alcohol–phenanthroline (1/1)
Crystals of the title compound, C(12)H(8)N(2)·C(7)H(8)O(2), were obtained during cocrystallization experiments of a compound with two hydrogen-bond donors (2-hydroxybenzyl alcohol) with another compound containing two hydrogen-bond acceptors (phenanthroline). Unexpectedly, the two molecules do not...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971015/ https://www.ncbi.nlm.nih.gov/pubmed/21578512 http://dx.doi.org/10.1107/S1600536809044699 |
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author | Ton, Cuong Quoc Bolte, Michael |
author_facet | Ton, Cuong Quoc Bolte, Michael |
author_sort | Ton, Cuong Quoc |
collection | PubMed |
description | Crystals of the title compound, C(12)H(8)N(2)·C(7)H(8)O(2), were obtained during cocrystallization experiments of a compound with two hydrogen-bond donors (2-hydroxybenzyl alcohol) with another compound containing two hydrogen-bond acceptors (phenanthroline). Unexpectedly, the two molecules do not form dimers with two O—H⋯N hydrogen bonds connecting the two molecules. However, one of the hydroxy groups forms a bifurcated hydrogen bond to both phenanthroline N atoms, whereas the other hydroxy group forms an O—H⋯O hydrogen bond to a symmetry-equivalent 2-hydroxybenzyl alcohol molecule. In addition, the crystal packing is stabilized by π–π interactions between the two phenanthroline ring systems, with a centroid–centroid distance of 3.570 Å. |
format | Text |
id | pubmed-2971015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29710152010-12-30 2-Hydroxybenzyl alcohol–phenanthroline (1/1) Ton, Cuong Quoc Bolte, Michael Acta Crystallogr Sect E Struct Rep Online Organic Papers Crystals of the title compound, C(12)H(8)N(2)·C(7)H(8)O(2), were obtained during cocrystallization experiments of a compound with two hydrogen-bond donors (2-hydroxybenzyl alcohol) with another compound containing two hydrogen-bond acceptors (phenanthroline). Unexpectedly, the two molecules do not form dimers with two O—H⋯N hydrogen bonds connecting the two molecules. However, one of the hydroxy groups forms a bifurcated hydrogen bond to both phenanthroline N atoms, whereas the other hydroxy group forms an O—H⋯O hydrogen bond to a symmetry-equivalent 2-hydroxybenzyl alcohol molecule. In addition, the crystal packing is stabilized by π–π interactions between the two phenanthroline ring systems, with a centroid–centroid distance of 3.570 Å. International Union of Crystallography 2009-10-31 /pmc/articles/PMC2971015/ /pubmed/21578512 http://dx.doi.org/10.1107/S1600536809044699 Text en © Ton and Bolte 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 Ton, Cuong Quoc Bolte, Michael 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title | 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title_full | 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title_fullStr | 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title_full_unstemmed | 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title_short | 2-Hydroxybenzyl alcohol–phenanthroline (1/1) |
title_sort | 2-hydroxybenzyl alcohol–phenanthroline (1/1) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971015/ https://www.ncbi.nlm.nih.gov/pubmed/21578512 http://dx.doi.org/10.1107/S1600536809044699 |
work_keys_str_mv | AT toncuongquoc 2hydroxybenzylalcoholphenanthroline11 AT boltemichael 2hydroxybenzylalcoholphenanthroline11 |