Structure, derivatisation, and metal complexation of p-cyclohexylcalix[4]arene

Chao Shen, Rene Z.H. Phe, Isabella Fong, Alexandre N. Sobolev, Mauro Mocerino, Massimiliano Massi, Mark I. Ogden

Research output: Contribution to journalArticlepeer-review

Abstract

Driven by an interest in the impact of the para-substituent of calix[4]arenes on metal complexation and structural chemistry, studies of p-cyclohexylcalix[4]arene (L) have been carried out. The 1:1 dichloromethane and dimethylformamide solvates were found to be isostructural, and different to the typical bilayer structure often observed for p-t-butylcalix[4]arene solvates. The methanol solvate, in contrast, does form a bilayered structure but is also a 1:1 solvate, unlike the p-t-butylcalix[4]arene·2MeOH system. Lanthanoid complexation was investigated, resulting in the structural characterisation of two different DMF solvates of a 2:2 dimeric europium complex, Eu2(L–3H)2(DMF)4. A tetrazole derivative, 5,11,17,23-tetracyclohexyl-25,27-dihydroxy-26,28-bis(tetrazole-5-ylmethoxy)calix[4]arene, has been synthesised via the intermediate 5,11,17,23-tetracyclohexyl-25,27-dihydroxy-26,28-dicyanomethoxycalix[4]arene, with the latter compound being structurally characterised. Attempts to isolate lanthanoid clusters supported by the tetrazole derivative under conditions known to form Ln19 clusters with the p-t-butyl analogue were unsuccessful, resulting only in isolation of the ligand from the reaction mixture.

Original languageEnglish
JournalSupramolecular Chemistry
DOIs
Publication statusE-pub ahead of print - 2021

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