Racemic and Enantiopure Camphene and Pinene Studied by the Crystalline Sponge Method
Author(s) -
Wester de Poel,
Paul Tinnemans,
Alexander L. L. Duchateau,
Maarten Honing,
Floris P. J. T. Rutjes,
Elias Vlieg,
R. De Gelder
Publication year - 2017
Publication title -
crystal growth and design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.966
H-Index - 155
eISSN - 1528-7505
pISSN - 1528-7483
DOI - 10.1021/acs.cgd.7b00942
Subject(s) - enantiopure drug , camphene , pinene , enantiomer , molecule , chemistry , sponge , organic chemistry , chromatography , enantioselective synthesis , geology , essential oil , catalysis , paleontology
The use of an achiral metal-organic framework for structure determination of chiral compounds is demonstrated for camphene and pinene. The structure of enantiopure β-pinene can be resolved using the crystalline sponge method. However, α-pinene cannot be resolved using enantiopure material alone because no ordering of guest molecules takes place in that case. Interestingly, enantiomeric pairs order inside the channels of the host framework when impure (+)-camphene is offered to the host, which is also the case when a racemic mixture of α-pinene is used. A mixture of (+)-α-pinene and (-)-β-pinene also leads to ordered incorporation in the host, showing the influence of the presence of an inversion center in the host framework. We further show that powder X-ray diffraction provides a direct view on incorporation of ordered guest molecules. This technique, therefore, provides a way to determine the optimal and/or minimal soaking time. In contrast, color change of the crystal only demonstrates guest uptake, not ordering. Moreover, we show that color change can also be caused by guest-induced host degradation.
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