0000000000616075

AUTHOR

Wei-er Liu

showing 3 related works from this author

Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Abstract Molecular recognition of aromatic hydrocarbons by four endo -functionalized molecular tubes has been studied by 1 H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅ π interactions.

chemistry.chemical_classificationhydrogen bond010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesmolecular dynamics0104 chemical sciencesMolecular recognitionmacrocycleschemistryhydrogenProton NMRhost-guest chemistryaromatic hydrocarbonhydrocarbonsmolecular recognitionAromatic hydrocarbonSpectroscopyHost–guest chemistryta116Binding selectivityChinese Chemical Letters
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Molecular recognition of aromatic hydrocarbons by four endo-functionalized molecular tubes has been studied by 1H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅π interactions. peerReviewed

hydrogen bondmacrocyclesvetyhost-guest chemistryaromatic hydrocarbonmolekyylidynamiikkamolecular recognitionhiilivedyt
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CCDC 1532334: Experimental Crystal Structure Determination

2017

Related Article: Guo-Bao Huang, Wei-Er Liu, Arto Valkonen, Huan Yao, Kari Rissanen, Wei Jiang|2018|Chin.Chem.Lett.|29|91|doi:10.1016/j.cclet.2017.07.005

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10183846-tetrabutoxy-30545860-tetraoxa-13154143-tetra-azatridecacyclo[47.7.1.1355.12529.12731.027.0611.01722.02126.03439.03559.04550.05357]hexaconta-246810171921232531(59)32343638454749(57)5052-icosaene-1442-dione 26-dibutoxyanthracene hydrateExperimental 3D Coordinates
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