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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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Autores principales: Ton, Cuong Quoc, Bolte, Michael
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
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.
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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
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AT boltemichael 2hydroxybenzylalcoholphenanthroline11