6533b7cffe1ef96bd1259af1

RESEARCH PRODUCT

Resorcarenes in the Boat Conformation as Building Blocks for Hydrogen-Bonded Assemblies Including Two Ammonium Cations

Volker BöhmerErkki KolehmainenErich F. PaulusKari RissanenAlexander Shivanyuk

subject

Hydrogen bondChemistryOrganic ChemistryCyclohexane conformationInorganic chemistrySupramolecular chemistryGeneral ChemistryResorcinareneChlorideCatalysisCrystallographyCalixarenemedicineMoleculeConformational isomerismmedicine.drug

description

Crystal structures are reported for various co-crystals of rccc-resorcarenes with triethylammonium chloride. Usually, two molecules of a C2v-symmetric tetraester 2 in the boat conformation are linked through four hydrogen-bonded chloride anions to give dimeric assemblies. Two of the chloride anions may be replaced by four hydrogen-bonded ethanol molecules in an otherwise similar structure. These assemblies, which consist of six or eight components, posses voluminous, negatively charged chambers in which two triethylammionium cations, 3+, are included as guests by strong electrostatic and hydrogen-bonding interactions. The host-guest N-H...Cl hydrogen bonds were clearly detected at 173 K. These are the first examples of hydrogen-bonded, solid-state capsules trapping two ions of the same charge in close proximity. In the 1:2 complex with 3+ Cl-, the molecule of the parent resorcarene 1 also adopts a boat conformation whose cavity is considerably extended by four hydrogen-bonded chloride anions. The pocket formed in this way again includes two 3+ ions as a result of electrostatic and hydrogen bonding host-guest interactions. All these structures show that the boat conformers of resorcarenes can be used as a novel motif for the construction of hydrogen-bonded assemblies capable of molecular inclusion and encapsulation.

https://doi.org/10.1002/1521-3765(20010504)7:9<1944::aid-chem1944>3.0.co;2-2