Crystallographic Analysis under Pressure Can Resolve Ambiguity Regarding Chirality: The Case of an Imidazolium-Based Coordination Network

Hydrostatic pressure can be a valuable aid in the structural study of a chiral compound, avoiding disorder and providing an unambiguous description of the stereochemistry of the chemical system. This follows from the single-crystal X-ray diffraction studies performed on the chiral framework [Y<sub>4</sub>(ox)<sub>5</sub>(L*)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>]·2.5H<sub>2</sub>O, <b>1</b> (L* = (<i>S</i>,<i>S</i>)-1,3-bis(carboxyethyl)imidazolium)), for hydrostatic pressures up to 3.6 GPa. The positional disorder for the chiral groups obtained at ambient pressure vanished when the crystal was subjected to hydrostatic pressure (2.4 GPa), unambiguously confirming the stereoisomer for all the chiral carbon centers and the homochiral nature of <b>1</b>.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-01-06
DOI
https://doi.org/10.1021/acs.inorgchem.5c05328
Citations
1
Primary Topic
Crystallography and molecular interactions
Type
article
Field-Weighted Citation Impact
26.05
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article

Crystallographic Analysis under Pressure Can Resolve Ambiguity Regarding Chirality: The Case of an Imidazolium-Based Coordination Network

Jean‐Pascal Sutter, Émilie Delahaye, Carine Duhayon
1 citations
Inorganic Chemistry
Crystallography and molecular interactions
26.05
article

Crystallographic Analysis under Pressure Can Resolve Ambiguity Regarding Chirality: The Case of an Imidazolium-Based Coordination Network

Jean‐Pascal Sutter, Émilie Delahaye, Carine Duhayon
article en
1 citations

Abstract

Hydrostatic pressure can be a valuable aid in the structural study of a chiral compound, avoiding disorder and providing an unambiguous description of the stereochemistry of the chemical system. This follows from the single-crystal X-ray diffraction studies performed on the chiral framework [Y<sub>4</sub>(ox)<sub>5</sub>(L*)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>]·2.5H<sub>2</sub>O, <b>1</b> (L* = (<i>S</i>,<i>S</i>)-1,3-bis(carboxyethyl)imidazolium)), for hydrostatic pressures up to 3.6 GPa. The positional disorder for the chiral groups obtained at ambient pressure vanished when the crystal was subjected to hydrostatic pressure (2.4 GPa), unambiguously confirming the stereoisomer for all the chiral carbon centers and the homochiral nature of <b>1</b>.

Inorganic ChemistryVol. 65(2)
Centre National de la Recherche Scientifique (FR), Laboratoire de Chimie de Coordination (FR)
Clean water and sanitation
Openalex Percentile: Top 3%
Crystallography and molecular interactions
26.05
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