Multicyclic Poly(ether ester)s by Polycondensation of Oligo(ethylene glycol)s and Trimesoyl Chloride

Monodisperse oligo(ethylene glycol)s were polycondensed with trimesoyl chloride using triethylamine as HCl acceptor. Despite nearly quantitative conversions and relatively high concentrations (0.4 mol/L), no gelation occurred with tri- and tetra(ethylene glycol), regardless of the feed ratio. With a feed ratio around 1.5/1.0 multicyclic poly(ether esters)s free of end groups were isolated and characterized by 1H NMR and MALDI-TOF mass spectrometry. At concentrations of 0.2 or 0.4 mol/L di-, penta-, and hexa(ethylene glycol)s yielded gels. At concentrations ≥ 0.2 mol/L exclusively gels were obtained from various α,ω-dihydroxyalkanes. However, soluble multicycles were obtained from 1,8-dihydroxy-3,6-dithiaoctane and from 1,4-bis(2-hydroxyethoxy)-2-butyne. The influence of conformational differences on the cyclization tendency is discussed. The multicycles derived from tri- and tetraethylene glycol showed cryptand properties and dissolved Li-, Na-, K-, and Cs-benzoate in tetrahydrofuran.