4.5 Article

Helicates with Ether-Substituted Catechol Esters as Ligands

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2020, Issue 32, Pages 5161-5172

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202000843

Keywords

Helicate; Templating; Molecular switch; Thermodynamics; Catecholate

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Mono- or biscatechol esters with ether-type substituents or spacers form either triple lithium bridged dimeric helicates or triple stranded helicates with the ability to bind three lithium cations in their interior. Hierarchical helicates with ether or thioether substituents show in solution a monomer-dimer equilibrium which is independent of the heteroatom in the ester substituent. However, dimerization constants are significantly lower than for corresponding alkyl derivatives. Dinuclear helicates with oligoether spacers are well obtained in the presence of lithium cations. Upon removal of the cations the helicates expand and successive addition of LiCl results in compression again.

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