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Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Diethyl [hydr-oxy(phen-yl)meth-yl]phospho-nate
Acta Crystallographica. Section E, Structure Reports Online
|January 5, 2011
Summary
This study reveals that molecules of C(11)H(17)O(4)P form chiral helical chains through hydrogen bonding. An ethyl group exhibits disorder, impacting crystal structure analysis.
Area of Science:
- Crystal Chemistry
- Supramolecular Chemistry
- Organic Phosphorus Chemistry
Background:
- Understanding the self-assembly of organic molecules is crucial for designing novel materials.
- Hydrogen bonding plays a significant role in dictating crystal packing and molecular architecture.
Purpose of the Study:
- To elucidate the crystal structure and intermolecular interactions of the title compound, C(11)H(17)O(4)P.
- To investigate the role of hydrogen bonding in the formation of supramolecular architectures.
Main Methods:
- Single-crystal X-ray diffraction analysis was employed to determine the molecular and crystal structure.
- Analysis of hydrogen bonding networks and identification of disordered moieties.
Main Results:
- Molecules of C(11)H(17)O(4)P self-assemble into chiral helical chains along the crystallographic b axis.
- O-H⋯O hydrogen bonds between hydroxyl and phosphonate groups facilitate the formation of these helical chains.
- One ethyl group displays positional disorder with site occupancy factors of approximately 0.7 and 0.3.
Conclusions:
- The study demonstrates the formation of one-dimensional chiral supramolecular chains driven by hydrogen bonding.
- The observed disorder in the ethyl group provides insights into conformational flexibility within the crystal lattice.
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