Circular Dichroisms of Mono- and Dibromo[2.2]paracyclophanes: A Combined Experimental and Theoretical Study.

ABSTRACT: Circular dichroisms (CDs) of planar chiral 4-bromo[2.2]paracyclophane (1) and three isomeric dibromo[2.2]paracyclophanes (p-2, m'-2, and o'-2) were investigated experimentally and theoretically. They all exhibited strong multisignate Cotton effects (CEs) at the ¹L_b, ¹L_a, and ¹B transitions of the component (bromo)benzene chromophore and were comparable to each other. For all of the cyclophanes examined, the enantiomer that eluted earlier from a chiral high-performance liquid chromatography column (Chiralcel IA or IB) exhibited negative and positive CEs at the ¹L_b and ¹L_a bands, respectively, which were followed by a more complicated pattern of CDs at the higher-energy bands. These CD features were well reproduced by quantum chemical calculations, allowing us to unambiguously assign the absolute configurations of the first-eluted enantiomers as R _p in all of the cases examined. Interestingly, the CDs of 1 and 2, although largely comparable in shape, were still sensitive to the number and pattern of bromine substitution, showing closer resemblance between m'-2 and o'-2 and between p-2 and 1. The theoretical calculations also reproduced successfully these spectral resemblance between them. The anisotropy (g) factors for the ¹L_b bands of these cyclophanes were considerably large (?10^-2), whereas those for the ¹L_a band were conventional in the order of 10^-3. In addition, a weak CE was observed in the low-energy region at around 320 nm, which turned out to originate from the interplanar interaction and is hence assigned to the "cyclophane band". The experimental g factors of this band were fairly large in the order of 10^-2, but the computation turned out to be quite challenging and were less well reproduced theoretically, ascribable to the forbidden nature of the transition.

SUBMITTER: Toda M 

PROVIDER: S-EPMC6641403 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature