Crystal structure ofcis-anti-cis-dicyclohexane-18-crown-6 acetonitrile disolvate

Author:

Nazarenko Alexander

Abstract

The title compound (systematic name:cis-anti-cis-2,5,8,15,18,21-hexaoxatricyclo[20.4.0.09,14]hexacosane acetonitrile disolvate), C20H36O6·2CH3CN, crystallizes from an acetonitrile solution of dicyclohexane-18-crown-6 on evaporation. The molecule is arranged around a center of symmetry with half the crown ether molecule and one molecule of acetonitrile symmetry independent. All O—C—C—O torsion angles aregauchewhile all C—O—C—C angles aretrans. The sequence of torsion angles is [(tg+t)(tgt)]3; the geometry of oxygen atoms is close to pseudo-D3dwith three atoms below and three atoms above the mean plane, with an average deviation of ±0.16 (1) Å from the mean plane. This geometry is identical to that observed in metal ion complexes of dicyclohexane-18-crown-6 but differs significantly from the conformation of a free unsolvated molecule. Each acetonitrile molecule connects to a crown ether moleculeviatwo of its methyl group H atoms (C—H...O). Weaker interactions exist between the third H atom of the acetonitrile methyl group and an O atom of a neighbouring crown ether molecule (C—H...O); and between the N atom of the acetonitrile molecule and a H atom of another neighbouring crown ether molecule. All these intermolecular interactions create a three-dimensional network stabilizing the disolvate.

Publisher

International Union of Crystallography (IUCr)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Reference11 articles.

1. Bruker (2013). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.

2. Bruker (2014). SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.

3. Isomer-dependent complexation of malononitrile by dicyclohexano-18-crown-6

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