0000000001302157

AUTHOR

Hua Ke

showing 12 related works from this author

Cover Picture: Achieving Strong Positive Cooperativity through Activating Weak Non‐Covalent Interactions (Angew. Chem. Int. Ed. 3/2018)

2018

chemistry.chemical_classificationchemistryStereochemistrySupramolecular chemistryCooperative bindingNon-covalent interactionsCover (algebra)CooperativityGeneral ChemistrySelf-assemblyHost–guest chemistryCatalysisAngewandte Chemie International Edition
researchProduct

Titelbild: Achieving Strong Positive Cooperativity through Activating Weak Non‐Covalent Interactions (Angew. Chem. 3/2018)

2017

chemistry.chemical_classificationchemistry010405 organic chemistryStereochemistryCooperative bindingNon-covalent interactionsGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAngewandte Chemie
researchProduct

Achieving Strong Positive Cooperativity through Activating Weak Non-Covalent Interactions

2018

Positive cooperativity achieved through activating weak non-covalent interactions is common in biological assemblies but is rarely observed in synthetic complexes. Two new molecular tubes have been synthesized and the syn isomer binds DABCO-based organic cations with high orientational selectivity. Surprisingly, the ternary complex with two hosts and one guest shows a high cooperativity factor (α=580), which is the highest reported for synthetic systems without involving ion-pairing interactions. The X-ray single-crystal structure revealed that the strong positive cooperativity likely originates from eight C-H⋅⋅⋅O hydrogen bonds between the two head-to-head-arranged syn tube molecules. Thes…

chemistry.chemical_classification010405 organic chemistryChemistryHydrogen bondStereochemistrycooperativitySupramolecular chemistrymolecular tubesCooperativityGeneral ChemistryDABCO010402 general chemistryhydorogenchemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundionsMoleculeNon-covalent interactionsmoleculesHost–guest chemistryTernary complexta116Angewandte Chemie International Edition
researchProduct

Directional Shuttling of a Stimuli-Responsive Cone-Like Macrocycle on a Single-State Symmetric Dumbbell Axle

2018

Rotaxane-based molecular shuttles are often operated using low-symmetry axles and changing the states of the binding stations. A molecular shuttle capable of directional shuttling of an acid-responsive cone-like macrocycle on a single-state symmetric dumbbell axle is now presented. The axle contains three binding stations: one symmetric di(quaternary ammonium) station and two nonsymmetric phenyl triazole stations arranged in opposite orientations. Upon addition of an acid, the protonated macrocycle shuttles from the di(quaternary ammonium) station to the phenyl triazole binding station closer to its butyl groups. This directional shuttling presumably originates from charge repulsion and an …

RotaxaneeducationTriazoleProtonation010402 general chemistry01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundbutyl groupssupramolekulaarinen kemiahost-guest chemistryrotaxanemoleculesta116Physicsmolecular machine010405 organic chemistrymolekyylitGeneral MedicineGeneral ChemistryMolecular machine0104 chemical sciencesMechanism (engineering)CrystallographyAxleMolecular shuttlechemistryDumbbellmacrocycleAngewandte Chemie International Edition
researchProduct

CCDC 1577841: Experimental Crystal Structure Determination

2018

Related Article: Yan-Long Ma, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|709|doi:10.1002/anie.201711077

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10163642-tetrabutoxy-132839505456-hexaoxatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaene dichloromethane solvateExperimental 3D Coordinates
researchProduct

CCDC 1575263: Experimental Crystal Structure Determination

2018

Related Article: Yan-Long Ma, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|709|doi:10.1002/anie.201711077

Space GroupCrystallographyCrystal System[2]-(11'-(pentane-15-diyl)bis(14-diazabicyclo[2.2.2]octan-1-ium))-(10163642-tetrabutoxy-132839505456-hexaoxatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaene)-rotaxane bis(hexafluorophosphate) acetonitrile solvateCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1575262: Experimental Crystal Structure Determination

2018

Related Article: Yan-Long Ma, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|709|doi:10.1002/anie.201711077

Space GroupCrystallography[3]-(11'-(decane-110-diyl)bis(14-diazabicyclo[2.2.2]octan-1-ium))-bis(10163642-tetrabutoxy-132839505456-hexaoxatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaene)-rotaxane bis(hexafluorophosphate) 12-dichloroethane acetonitrile solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

Achieving Strong Positive Cooperativity through Activating Weak Non‐Covalent Interactions

2023

researchProduct

CCDC 1826426: Experimental Crystal Structure Determination

2018

Related Article: Jie‐Shun Cui, Qian‐Kai Ba, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|7809|doi:10.1002/anie.201803349

Space GroupCrystallography[2]-(N1-((35-di-t-butylphenyl)methyl)-N6-((4-(1-((35-di-t-butylphenyl)methyl)-1H-123-triazol-4-yl)phenyl)methyl)-N1N1N6N6-tetramethylhexane-16-diaminium)-(10163642-tetrabutoxy-28505456-tetraoxa-1339-diazoniatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaene)-rotaxane trifluoroacetate tris(hexafluorophosphate) acetone methanol dichloromethane solvate monohydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1828064: Experimental Crystal Structure Determination

2018

Related Article: Jie‐Shun Cui, Qian‐Kai Ba, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|7809|doi:10.1002/anie.201803349

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10163642-tetrabutoxy-28505456-tetraoxa-1339-diazatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaeneExperimental 3D Coordinates
researchProduct

CCDC 1577842: Experimental Crystal Structure Determination

2018

Related Article: Yan-Long Ma, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|709|doi:10.1002/anie.201711077

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10163642-tetrabutoxy-132839505456-hexaoxatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)30323436414345(53)4648-icosaeneExperimental 3D Coordinates
researchProduct

CCDC 1826427: Experimental Crystal Structure Determination

2018

Related Article: Jie‐Shun Cui, Qian‐Kai Ba, Hua Ke, Arto Valkonen, Kari Rissanen, Wei Jiang|2018|Angew.Chem.,Int.Ed.|57|7809|doi:10.1002/anie.201803349

Space GroupCrystallography10163642-tetrabutoxy-28505456-tetraoxa-1339-diazatridecacyclo[43.7.1.1351.12327.12529.027.0611.01520.01924.03237.03355.04146.04953]hexapentaconta-246810151719212329(55)303234364143454749(53)-icosaene dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct