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   <subfield code="a">The title macrocycle 1 was synthesised in good yield (66%) by a one-pot condensation process from 2,3-bis(chloromethyl)-p-xylene andN,N′-ditosylethylendiamine. The macrocycle was found to undergo isomerization processes at elevated temperature on the NMR time scale (ΔG≠ = 87.8 kJ mol−1) and acts as a suitable host only for toluene. The FAB-MS spectra of1 is rich, and full of interesting and very diagnostic fragmentation pathways.</subfield>
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