(+)-syn-Benzotriborneol forms stable complexes with one molecule of water. This is due to the ability of the host to form three hydrogen bonds with water, to act simultaneously as a hydrogen-bond acceptor and donor, and to a perfect geometrical match between the pair. We report experimental (X-ray and neutron diffraction, VT NMR, DSC, TGA) and stereochemical studies carried out to elucidate and quantify the molecular and thermodynamic aspects of this supramolecular complex.

(+)-syn-Benzotriborneol an enantiopure C(3)-symmetric receptor for water

Crisma M;
2012

Abstract

(+)-syn-Benzotriborneol forms stable complexes with one molecule of water. This is due to the ability of the host to form three hydrogen bonds with water, to act simultaneously as a hydrogen-bond acceptor and donor, and to a perfect geometrical match between the pair. We report experimental (X-ray and neutron diffraction, VT NMR, DSC, TGA) and stereochemical studies carried out to elucidate and quantify the molecular and thermodynamic aspects of this supramolecular complex.
2012
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
Inglese
10
2464
2469
Sì, ma tipo non specificato
CUP-SHAPED MOLECULES; C-3 SYMMETRY; RECOGNITION; BINDING; CYCLOTRIMERIZATION; COMPLEXATION; CONSTRUCTION; CAVITANDS; DIMER
1
info:eu-repo/semantics/article
262
Fabris F.; De Lucchi O.; Nardini I.; Crisma M.; Mazzanti A.; Mason S.A.; LeméèCailleau M.H.; Scaramuzzo F.A.; Zonta C.
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/232674
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