GEOMETRICAL ISOMERIZATION OF CAROTENOIDS IN DICHLOROMETHANE

In a 3 mmol dm(-3) solution of all-trans-canthaxanthin (I) in HPLC gra de dichloromethane cis-isomers are formed. Optical absorptions due to cis-isomers in addition to those due to an intermediate are observed i n 3 mmol dm(-3) solutions of all-trans-beta-carotene(II) and 8'-apo-be ta-caroten-8'-al (III), as a result of 0.1-0.2 mmol dm(-3) acid normal ly found in HPLC grade dichloromethane. The cis-isomers were separated by HPLC and characterized by optical and NMR spectroscopic techniques . AM1 calculations performed on the ground state and protonated I show ed that 9-cis and 13-cis-isomers will be formed by acid induced isomer ization in greater yield than other cis and cis,cis-isomers. This was observed experimentally. If an excess amount of hydrochloric acid (sim ilar to 1 mol dm(-3)) is added to the solution of dichloromethane cont aining the carotenoids. radical cations of the carotenoids are formed.