Solid-state compounds of stereoisomers: cis and trans isomers of 1,2-cyclohexanediol and 2,3-tetralindiol

Lloyd, M.A.; Patterson, G.E.; Simpson, G.H.; Duncan, L.L.; King, D.P.; Fu, Y.; Patrick, B.O.; Parkin, S.; Brock, C.P.

doi:10.1107/S0108768107010579

Acta Crystallographica Section B
Acta Crystallographica
Section B STRUCTURAL SCIENCE, CRYSTAL ENGINEERING AND MATERIALS

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Figure 9
Projections of the stacks of 2,3-tetralindiol molecules in (blue) the fully ordered compound of cis and R,R molecules, and (red) the enantiomerically pure trans compound (S,S enantiomers). The molecules on the left are molecule B (cis isomer) of the compound and molecule B of the pure S,S enantiomer. (a) Projection down the stack. The view direction is b for the compound and c for the pure enantiomer. (b) Projections related to those in part (a) by a 90° rotation around the horizontal. The choice of enantiomer has little effect on the drawings.

STRUCTURAL SCIENCE
CRYSTAL ENGINEERING
MATERIALS

ISSN: 2052-5206

Volume 63| Part 3| May 2007| Pages 433-447

doi:10.1107/S0108768107010579

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