Structural comparisons of the binding cores formed by 1,3-di-Amide derivatives of p-tert-Butylcalix[4]arene: arms stabilization through Intra-molecular interactions including N-H***O, O-H***Cl and π***Cl types
hal.structure.identifier | Bioinorganic Laboratory, Department of Chemistry | |
dc.contributor.author | DEY, Mishtu | |
hal.structure.identifier | Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB] | |
dc.contributor.author | GUIONNEAU, Philippe | |
hal.structure.identifier | Bioinorganic Laboratory, Department of Chemistry | |
dc.contributor.author | HINGE, Vijaya Kumar | |
hal.structure.identifier | Bioinorganic Laboratory, Department of Chemistry | |
dc.contributor.author | RAO, Chebrolu P. | |
dc.date.issued | 2014 | |
dc.identifier.issn | 0369-8203 | |
dc.description.abstractEn | his paper deals with the development of a receptor with selectively functionalized at the lower rim of p-tert-butyl calix[4]arene linked through amide bond, resulting in the diamide derivatives (L 1 , L 2 and L 3 ) suitable for sensing ions and molecules. All the derivatives were thoroughly characterized by analytical and spectral methods. These derivatives were structurally characterized by single crystal X-ray diffraction and the conformational features of the calix[4]arene as well as the pendants are discussed. The L 1 and L 2 exhibited intramolecular hydrogen bond interaction between the N-H and the lower rim phenolic oxygen in addition to the circular hydrogen bonding between the phenolic O-H and the ether oxygen of the adjacent strand. The corresponding H-bond is absent when no 'H' is present on amide-N as in case of L 3 . Such intramolecular N-H***O interactions observed with the pendant results in a conformational bend responsible for the orientation of the arms and there by the nature of the binding core formed. Thus the binding cores formed differ largely between L 3 and the other two. | |
dc.language.iso | en | |
dc.publisher | Springer | |
dc.subject.en | p-tert-Butyl calix[4]arene | |
dc.subject.en | 3-di-Amide derivative | |
dc.subject.en | Single crystal | |
dc.subject.en | X-ray diffraction | |
dc.subject.en | Molecular recognition | |
dc.subject.en | Intramolecular hydrogen bond | |
dc.title.en | Structural comparisons of the binding cores formed by 1,3-di-Amide derivatives of p-tert-Butylcalix[4]arene: arms stabilization through Intra-molecular interactions including N-H***O, O-H***Cl and π***Cl types | |
dc.type | Article de revue | |
dc.identifier.doi | 10.1007/s40010-014-0145-5 | |
dc.subject.hal | Chimie/Matériaux | |
bordeaux.journal | Proceedings of the National Academy of Sciences, India Section A: Physical Sciences | |
bordeaux.page | 297-303 | |
bordeaux.volume | 84 | |
bordeaux.issue | 2 | |
bordeaux.peerReviewed | oui | |
hal.identifier | hal-01003800 | |
hal.version | 1 | |
hal.popular | non | |
hal.audience | Internationale | |
hal.origin.link | https://hal.archives-ouvertes.fr//hal-01003800v1 | |
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