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By the reaction of para‐formylcalix[4]arenes 1–6 with trialkyl phosphites in the presence of dry hydrogen chloride, calix[4]arenes 7–13 possessing dialkylphosphoryl‐hydroxymethyl groupings at the upper rim were synthesized. Calix[4]arenes 18–23 functionalized with dialkylphosphoryl‐alkyl(aryl)aminomethyl groups were obtained by sodium‐promoted addition of dialkyl phosphites to C=N bonds of para‐iminocalix[4]arenes 14–17. The consecutive treatment of α‐hydroxy‐ or α‐aminophosphonic acid dialkyl esters of calix[4]arenes 7, 10, 18, and 21 with bromotrimethylsilane and methanol gave dihydroxyphosphoryl derivatives of calix[4]arenes 24–27. It was shown that calix[4]arenes bearing at the macrocyclic upper rim hydroxymethylphosphonic fragments, as well as bis‐hydroxymethyl(aminomethyl)phosphonic fragments, are able to undergo self‐assembly with formation of dimeric OH···O=P hydrogen bonded associates.
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Solovyov et al. (2001) studied this question.
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