http://www.cnr.it/ontology/cnr/individuo/prodotto/ID195138
Synthetic Tripodal Receptors for Carbohydrates. Pyrrole, a Hydrogen Bonding Partner for Saccharidic Hydroxyls (Articolo in rivista)
- Type
- Label
- Synthetic Tripodal Receptors for Carbohydrates. Pyrrole, a Hydrogen Bonding Partner for Saccharidic Hydroxyls (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/jo301341c (literal)
- Alternative label
O. Francesconi, M. Gentili, S. Roelens (2012)
Synthetic Tripodal Receptors for Carbohydrates. Pyrrole, a Hydrogen Bonding Partner for Saccharidic Hydroxyls
in Journal of organic chemistry
(literal)
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- O. Francesconi, M. Gentili, S. Roelens (literal)
- Pagina inizio
- Pagina fine
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- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Chimica, Universita' di Firenze; Istituto di Metodologie Chimiche (IMC), Consiglio Nazionale delle Ricerche (CNR). (literal)
- Titolo
- Synthetic Tripodal Receptors for Carbohydrates. Pyrrole, a Hydrogen Bonding Partner for Saccharidic Hydroxyls (literal)
- Abstract
- The carbohydrate recognition properties of synthetic tripodal receptors
relying on H-bonding interactions have highlighted the crucial role played by the functional
groups matching saccharidic hydroxyls. Herein, pyrrole and pyridine, which emerged as two
of the most effective H-bonding groups, were quantitatively compared through their
isostructural substitution within the architecture of a shape-persistent bicyclic cage receptor.
NMR and ITC binding studies gave for the pyrrolic receptor a 20-fold larger affinity toward
octyl-beta-D-glucopyranoside in CDCl3, demonstrating the superior recognition properties of
pyrrole under conditions in which differences would depend on the intrinsic binding ability
of the two groups. The three-dimensional structures of the two glucoside complexes in
solution were elucidated by combined NMR and molecular mechanics computational
techniques, showing that the origin of the stability difference between the two closely similar
complex structures resides in the ability of pyrrole to establish shorter/stronger H-bonds
with the glucosidic ligand compared to pyridine (literal)
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