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Absolute structure determination as a reference for the enantiomeric resolution of racemic mixtures of cyclophosphazenes via chiral high-performance liquid chromatography

Absolute structure determination as a reference for the enantiomeric resolution of racemic mixtures of cyclophosphazenes via chiral high-performance liquid chromatography
Absolute structure determination as a reference for the enantiomeric resolution of racemic mixtures of cyclophosphazenes via chiral high-performance liquid chromatography
Reversed-phase chiral high-performance liquid chromatography (HPLC) is a potentially powerful technique for the enantiomeric resolution of racemic mixtures, although the elution order of enantiomers is only relative and it is necessary to fully characterize reference systems for this method to provide absolute configurational information. The enantiomeric resolution of a series of racemic di-spiro cyclotriphosphazene derivatives, N3P3X2[O(CH2)(3)NH]2 (X = Cl, Ph, SPh, NHPh, OPh) [(1)-(5), respectively] was carried out by reversed-phase chiral HPLC on a commercially available Pirkle-type chiral stationary phase (R,R)-Whelk-01 using 85:15 (v/v) hexane-thf as the mobile phase. The absolute configurations of the resulting enantiomers of compounds (3) (X = SPh) and (5) (X = OPh) were determined unambiguously by X-ray crystallography. For both (3) and (5) it was found that the SS enantiomer eluted before the RR enantiomer, indicating a convenient method to determine the absolute configurations of enantiomers of this series of cyclophosphazene derivatives and providing the first set of enantiomeric reference compounds for cyclophosphazene derivatives. These structures demonstrate an interesting anomaly in that the pair of enantiomers of (3) crystallize in enantiomorphically paired space groups whilst, under the same conditions, the solid-state forms of the enantiomers of (5) form structures in Sohncke space groups that are not enantiomorphous.
cyclotriphosphazene derivatives, enantiomers, absolute configuration, x-ray crystallography, chiral hplc
0108-7681
355-362
Coles, Simon
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Davies, David
da29ccb1-e7a5-4e8a-ba17-34fe625d6fc8
Hursthouse, Michael
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Yeşilot, Serkan
6d82d5b6-173c-4ca4-bf2e-02676c18c8d0
Çoşut, Bünyemin
bb661ad6-f92c-4fe5-a81e-ec378009ef6b
Kılıç, Adem
565a42ec-2d18-4142-8b37-bb74b244b2f5
Coles, Simon
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Davies, David
da29ccb1-e7a5-4e8a-ba17-34fe625d6fc8
Hursthouse, Michael
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Yeşilot, Serkan
6d82d5b6-173c-4ca4-bf2e-02676c18c8d0
Çoşut, Bünyemin
bb661ad6-f92c-4fe5-a81e-ec378009ef6b
Kılıç, Adem
565a42ec-2d18-4142-8b37-bb74b244b2f5

Coles, Simon, Davies, David, Hursthouse, Michael, Yeşilot, Serkan, Çoşut, Bünyemin and Kılıç, Adem (2009) Absolute structure determination as a reference for the enantiomeric resolution of racemic mixtures of cyclophosphazenes via chiral high-performance liquid chromatography. Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 65 (3), part 3, 355-362. (doi:10.1107/S0108768109006120). (PMID:19461146)

Record type: Article

Abstract

Reversed-phase chiral high-performance liquid chromatography (HPLC) is a potentially powerful technique for the enantiomeric resolution of racemic mixtures, although the elution order of enantiomers is only relative and it is necessary to fully characterize reference systems for this method to provide absolute configurational information. The enantiomeric resolution of a series of racemic di-spiro cyclotriphosphazene derivatives, N3P3X2[O(CH2)(3)NH]2 (X = Cl, Ph, SPh, NHPh, OPh) [(1)-(5), respectively] was carried out by reversed-phase chiral HPLC on a commercially available Pirkle-type chiral stationary phase (R,R)-Whelk-01 using 85:15 (v/v) hexane-thf as the mobile phase. The absolute configurations of the resulting enantiomers of compounds (3) (X = SPh) and (5) (X = OPh) were determined unambiguously by X-ray crystallography. For both (3) and (5) it was found that the SS enantiomer eluted before the RR enantiomer, indicating a convenient method to determine the absolute configurations of enantiomers of this series of cyclophosphazene derivatives and providing the first set of enantiomeric reference compounds for cyclophosphazene derivatives. These structures demonstrate an interesting anomaly in that the pair of enantiomers of (3) crystallize in enantiomorphically paired space groups whilst, under the same conditions, the solid-state forms of the enantiomers of (5) form structures in Sohncke space groups that are not enantiomorphous.

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More information

Published date: June 2009
Keywords: cyclotriphosphazene derivatives, enantiomers, absolute configuration, x-ray crystallography, chiral hplc
Organisations: Organic Chemistry: Synthesis, Catalysis and Flow

Identifiers

Local EPrints ID: 149253
URI: http://eprints.soton.ac.uk/id/eprint/149253
ISSN: 0108-7681
PURE UUID: 4449d07e-0145-4766-8dcc-5b2881674b8c
ORCID for Simon Coles: ORCID iD orcid.org/0000-0001-8414-9272

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Date deposited: 04 May 2010 14:00
Last modified: 14 Mar 2024 02:43

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Contributors

Author: Simon Coles ORCID iD
Author: David Davies
Author: Serkan Yeşilot
Author: Bünyemin Çoşut
Author: Adem Kılıç

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