2004•CrystEngCommRequires access

The crystal structure of an unstable polymorph of β- d -allose

Pierre A. Bonnet, Jacco van de Streek, Andrew V. Trask, W. D. Samuel Motherwell, William Jones

Open publisher page 10 citations

Abstract

The crystal structure of a new polymorph, Form II, of β-D-allose has been determined by X-ray powder diffraction. The unit cell is hexagonal, a = b = 16.598 Å, c = 4.856 Å, α = β = 90°, γ = 120°, space group P62 with Z = 6, Z′ = 1. The molecule adopts the 4C1 chair-conformation, with a torsional change of conformation of the O6 side-chain compared to the orthorhombic Form I. The two polymorphs share a common feature of a stacked hydrogen bonded column of molecules in the short axis direction. The structures differ in hydrogen linking of these columns. The more stable Form I has more immediate neighbours linked by hydrogen bonds to a reference molecule, and higher crystal density than Form II.

About this research paper

What this paper is about

The crystal structure of a new polymorph, Form II, of β-D-allose has been determined by X-ray powder diffraction. The unit cell is hexagonal, a = b = 16.598 Å, c = 4.856 Å, α = β = 90°, γ = 120°, space group P62 with Z = 6, Z′ = 1. The molecule adopts the 4C1 chair-conformation, with a torsional change of conformation of the O6 side-chain compared to the orthorhombic Form I. The two polymorphs share a common feature of a stacked hydrogen bonded column of molecules in the short axis direction. The structures differ in hydrogen linking of these columns. The more stable Form I has more immediate neighbours linked by hydrogen bonds to a reference molecule, and higher crystal density than Form II.

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The crystal structure of a new polymorph, Form II, of β-D-allose has been determined by X-ray powder diffraction. The unit cell is hexagonal, a = b = 16.598 Å, c = 4.856 Å, α = β = 90°, γ = 120°, space group P62 with Z = 6, Z′ = 1. The molecule adopts the 4C1 chair-conformation, with a torsional change of conformation of the O6 side-chain compared to the orthorhombic Form I. The two polymorphs share a common feature of a stacked hydrogen bonded column of molecules in the short axis direction. The structures differ in hydrogen linking of these columns. The more stable Form I has more immediate neighbours linked by hydrogen bonds to a reference molecule, and higher crystal density than Form II.

Key concepts: Orthorhombic crystal system, Crystallography, Hydrogen bond, Molecule, Crystal structure, Chemistry, Crystal (programming language), Hexagonal crystal system

Related papers

Back to paper searchBrowse research topicsOriginal source
The crystal structure of an unstable polymorph of β- d -allose — Research Paper | ScholarLens