International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anions, cations, and neutral pairs, combining both cation-pi and anion-pi interaction sites, were investigated to probe the complexity of interfering weak intermolecular interactions. It is suggested from NMR experiments, and supported by CASSCF/CASPT2 calculations, that the binding constants of anions can be modulated by a factor of up to 100 by varying the fluorination sites on the electron-poor aromatic rings. Interestingly, this subtle chemical modification can also reverse the sign of cooperativity in ion-pair recognition. Wavefunction calculations highlight how short-and long-range interactions interfere in this recognition process, suggest...
We report that anion−π and cation−π interactions can occur on the same aromatic surface. Interaction...
[eng] Supramolecular chemistry is a field of scientific exploration that probes the relationship bet...
Cations bind to the π face of an aromatic structure through a surprisingly strong, noncovalent force...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe heteroditopic hemicryptophane 1, which bears a tripodal anion binding site...
We describe a large number of binding studies in aqueous media designed to provide new insights into...
We describe a large number of binding studies in aqueous media designed to provide new insights into...
International audienceBrothers and enemies: Anion–π and cation–π interactions act in a synergistic w...
International audienceThe heteroditopic hemicryptophane 1, which bears a tripodal anion binding site...
We report that anion−π and cation−π interactions can occur on the same aromatic surface. Interaction...
Cations bind to the π face of an aromatic structure through a surprisingly strong, noncovalent force...
We report that anion−π and cation−π interactions can occur on the same aromatic surface. Interaction...
[eng] Supramolecular chemistry is a field of scientific exploration that probes the relationship bet...
Cations bind to the π face of an aromatic structure through a surprisingly strong, noncovalent force...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe recognition properties of heteroditopic hemicryptophane hosts towards anio...
International audienceThe heteroditopic hemicryptophane 1, which bears a tripodal anion binding site...
We describe a large number of binding studies in aqueous media designed to provide new insights into...
We describe a large number of binding studies in aqueous media designed to provide new insights into...
International audienceBrothers and enemies: Anion–π and cation–π interactions act in a synergistic w...
International audienceThe heteroditopic hemicryptophane 1, which bears a tripodal anion binding site...
We report that anion−π and cation−π interactions can occur on the same aromatic surface. Interaction...
Cations bind to the π face of an aromatic structure through a surprisingly strong, noncovalent force...
We report that anion−π and cation−π interactions can occur on the same aromatic surface. Interaction...
[eng] Supramolecular chemistry is a field of scientific exploration that probes the relationship bet...
Cations bind to the π face of an aromatic structure through a surprisingly strong, noncovalent force...