Solid-state conformations and absolute configurations of (+) and (−) α-, β-, and γ-hexabromocyclododecanes (HBCDs)

Hexabromocyclododecanes (HBCDs) are high production volume chemicals used as flame retardants for plastics and textiles. They are currently produced in quantities exceeding 20 000 t/y. Despite this fact, the correct stereochemistry of most HBCDs is still not known. Six stereocenters are formed during bromination of cyclododecatrienes, resulting in mixtures of different stereoisomers. Considering all elements of symmetry, 16 different stereoisomers including six pairs of enantiomers as well as 4 meso forms are possible theoretically. Recently, we isolated 8 of the 16 possible stereoisomers from a technical HBCD mixture and assigned their relative configurations. Herein, we report on the isolation of 6 enantiomerically pure α-, β-, and γ-HBCDs, obtained from preparative chiral-phase liquid chromatography, and we present their absolute configurations, which were determined from X-ray diffraction analysis. The absolute configuration of (−) α-HBCD was found to be (1 R,2 R,5 S,6 R,9 R,10 S), while the one of (+) β-HBCD is assigned to (1 S,2 S,5 S,6 R,9 S,10 R), whereas the one of (−) γ-HBCD corresponds to (1 S,2 S,5 S,6 R,9 R,10 S). The given structural information allows the unambiguous identification of the six most important HBCD stereoisomers, which typically account for more than 95% of technical HBCDs. In addition, we compared the solid-state conformations of racemic and enantiomerically pure α-, β-, and γ-HBCDs. In all cases, vicinal dibromides adopted a synclinal (sc) conformation with torsion angles of 69 ± 6°. A unique structural motive was common to all examined HBCD solid-state conformations. This conserved structure was described as an extended triple turn consisting of an arrangement of three pairs of synclinal and two antiperiplanar torsion angles.