Abstract
Chlorination of triphenylene (1a) employing a mixture of aluminium trichloride and sulphur monochloride in sulphuryl chloride leads to rearrangement with formation of the title chlorocarbon (2), a new host, as main product. X-ray crystal structure analyses of the unsolvated spirocycle (2) as well as of its inclusion compounds with guests benzene and cyclohexa-1,4-diene are described.
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