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RESEARCH PRODUCT
Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*
Pia JurčekRakesh PuttreddyJohn F. TrantRobin H. A. RasKari RissanenLotta TurunenNgong Kodiah Beyehsubject
crystal structurekemiaSupramolecular chemistryCrystal structurechemistry010402 general chemistry01 natural scienceschemistry.chemical_compoundPolymer chemistryPyridinecrystalssupramolekulaarinen kemiaAcetoneresorcinarenesmoleculesIsoquinolineta116Biochemistry Biophysics and Structural Biologyvetysidoksetta114010405 organic chemistryHydrogen bondQuinolinemolekyylitGeneral Chemistrykiteet0104 chemical sciencesaromatic N-oxidesSolventChemistrychemistryvetyhydrogenhydrogen bondsSupramolecular chemistrydescription
The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional self-included chains. Of special note, crystallising C-propyl-2-bromoresorcinarene with 3-methylpyridine N-oxide from acetone results in a 2:2 dimeric capsular assembly organised through both C−H···πhost and N−O···(H−O)host interactions. peerReviewed
year | journal | country | edition | language |
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2018-01-01 | SUPRAMOLECULAR CHEMISTRY |