Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols

Literature Information

Publication Date 2003-01-21
DOI 10.1039/B209427D
Impact Factor 3.876
Authors

Amelia García Fraile, David G. Morris, Antonio García Martínez, Santiago de la Moya Cerero, Kenneth W. Muir, Karl S. Ryder, Enrique Teso Vilar


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Abstract

Our interest in the relationship between the hydrogen bonding motifs displayed by monoalcohols and the properties of the solids which contain these motifs has led us to determine the crystal structures of three polycyclic bridgehead monoalcohols. One C10H16O isomer crystallises in the space group P212121 but the three molecules which comprise the asymmetric unit are related approximately by the operations of a 31 screw axis. They are linked by hydrogen bonds to form an infinite helix. A second C10H16O isomer forms rings containing four molecules joined by cooperative hydrogen bonds. The chiral space group P41212 accommodates molecules of the S,S and R,R enantiomers in the molar ratio 92 ∶ 8 (ee 84%) owing to disorder. A related C9H14O2 keto-alcohol forms infinite chains by C–OH⋯OC hydrogen bonding. These hydrogen bond motifs are shown to be typical for 45 tertiary monoalcohols, CmHnOH, present in the Cambridge Structural Database. Tertiary monoalcohols display in a more pronounced form the strong preferences for trigonal and tetragonal space groups and for asymmetric units containing several molecules which are established features of the crystallochemistry of monoalcohols.

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Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
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Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

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