Abstract

The cyclo cocondensation of triethylenetetramine with arylpyruvaldehydes is templated by iron(III) chloride, to give a [12]aneN4 type diimine complex intermediate which may be reduced and demetallated in situ with sodium borohydride giving the saturated [12]aneN4 metal-free macrocycle in up to 60% overall yields; photophysical studies are used to demonstrate the similarity between the aryl functionalised [12]aneN4 derivatives formed by this route and analogues derived from [12]aneN4 itself.

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